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Operations Manager
Manufacturing & Production - Phoenix, AZ 85323

Job Purpose: Provide direction and leadership to the Southwest manufacturing facility to achieve company goals and objectives. This position will be responsible for all aspects of the plant including safety, environmental, developing people, quality, productivity, cost and facility management. Additionally, the role is responsible for planning, coordinating, organizing and controlling production, as well as continuously improving manufacturing processes to ensure the highest quality product with the total lowest cost to meet and exceed the expectatio...

View Operations Manager Job - Phoenix, AZ 85323
operations manager, plant manager, director of manufacturing,
Clinical Biostatistician (onsite/offsite)
Science & Biotech - San Diego, CA 92122

Contract Biostatistician, onsite/offsite, San Diego, CA - 1 year renewable contract - 20/30 hours per week; possibly can increase according to workload - Prefer at least 50% onsite, or 1 day onsite. Alternatively, onsite for initial training and able to come onsite as needed. Summary: The Project Statistician works extensively with Clinical Data Management, Science Team, and other project team members to effectively communicate data findings to the data manager and project team, including client clinicians and statisticians. The successful cand...

View Clinical Biostatistician (onsite/offsite) Job - San Diego, CA 92122
establish statistical processes, Prepare or provide input into statistical sections of protocols, including sample size calculations, randomization specifications and verify randomization codes, provide specifications for safety and efficacy analysis datasets to programmers,proficient in SAS and able to program using SAS macro language.
Remote Safety SAS programmer (ISS/ISE)
Science & Biotech - Home Based, CA 94101

Remote Clinical SAS programmer need, open ended contract SAS programmer with 5+ years of experience as a Clinical Research SAS Programmer. Experience with integrate safety analysis and reporting (ISS/CSS) is preferred. Provide programming support for Global Safety activities related to clinical trials data: - Follow company’s SOP and process guidelines, creation and maintenance of programs used for aggregate data creation, management, data validation, statistical report (TFLs – Tables/Figures/Listings) generation, and program validation. - T...

View Remote Safety SAS programmer (ISS/ISE) Job - Home Based, CA 94101
CDISC, SAS, SDTM, ADaM, tables, listings, figures, macros, graphs, validation, safety, efficacy, ISS, ISE, global safety
Plant Manager
Manufacturing & Production - Lapeer, MI 48446

Our client has a plant located about 10 minutes from Lapeer MI. They're in search of a strong leader for Plant Manager over ~50 nonunion employees. This job requires experience with P&L, quality, supply chain, maintenance, etc. Being this is a smaller plant you will be involved with all aspects of making sure the plant runs smoothly. This is a great company, and outstanding hiring manager, an excellent long-term and short term career path, very competitive pay, a strong bonus and an excellent relocation package. The next move in this company wou...

View Plant Manager Job - Lapeer, MI 48446
plant manager, manufacturing, processing, packaging, minerals, chemical, engineer
SAS Analyst- contract
Other - St. Augustine, FL 32080

TalentMine is actively looking for a SAS Programming analyst for a long term contract opportunity with a client in the Pharmaceutical industry. This is an onsite position supporting SAS system application rollout to Research and Development. For more details please e-mail resumes to Requirements: Experience specializing in SAS Enterprise Guide Administration Will provide SAS administration and analysis and application program support for multiple applications in a Research and Development environment Must have ex...

View SAS Analyst- contract Job - St. Augustine, FL 32080
SAS Analyst, Unix, Linux, SQL, Access
Consulting Director, Consumer Goods
Management & Business - Dallas, TX 75201

Consulting Director – Consumer Packaged Goods - Dallas The Company Cognizant (NASDAQ:CTSH) is a leading provider of information technology, consulting, and business process outsourcing services, dedicated to helping the world's leading companies build stronger businesses. Headquartered in Teaneck, New Jersey (U.S.), Cognizant has over 160,000 employees as of March 31, 2013. Cognizant is a member of the NASDAQ-100, the S&P 500, the Forbes Global 1000, and the Fortune 500 and is ranked among the top performing and fastest growing companies in the wo...

View Consulting Director, Consumer Goods Job - Dallas, TX 75201
Clinical Development Scientist / Clinical Research Scientist
Science & Biotech - King of Prussia, PA 19406

An excellent sponsor company in King of Prussia, PA is seeking an experienced and talented Clinical Development Scientist to join their team. The Clinical Development Scientist’s principal responsibly will be to assist with the drafting of core protocols, CRF’s, and analytical plans through discussions with matrix team members. They will also assist with drafting assigned sections of clinical reports, dossiers, and other clinical documents. Additional responsibilities will include, but are not limited to the following: • Reviews standard for...

View Clinical Development Scientist / Clinical Research Scientist Job - King of Prussia, PA 19406
Clinical Development Scientist, Clinical Scientist, Clinical Research Scientist, writing, write, draft, drafting, protocol, protocols, CRF’s, case report forms, clinical reports, clinical study reports, dossiers, drug supply, investigator brochures, investigator meetings, report, reports, standard reply, standard replies, training materials, investigational new drug, new drug applications, IND, NDA, INDs, NDAs, manuscripts, abstracts
Toronto CRA
Science & Biotech - Detroit, MI 48201

We are currently seeking candidates that reside in Canada. Clinical Research Associates with Oncology experience to manage sites in Greater Toronto area. Responsibilites include: Responsible for executing activities within site initiation and start-up, site monitoring, site management and site/study close-out. Contributes to site level recruitment strategy and contingency planning and implementation in partnership with other functional areas to achieve clinical research target. Ensures that all AEs/SAEs/PQCs are reported within the required repo...

View Toronto CRA Job - Detroit, MI 48201
Oncology, Rish based Monitoring, CRA, Clinical Research Associate, Source Data Verification
TMF Compliance Specialist
Science & Biotech - Raritan, NJ 08869

A large pharmaceutical company in Central NJ has an immediate need for a TMF Compliance Specialist. This position will be responsible for supporting clinical trial audits and inspections. This person will serve as the point of contact and will participate in the support of TMF management Q&A. Other responsibilities may include, but are not limited to the following: • Review TMF and eTMF for completeness at a high level • Identify trends in the organization using eTMF reporting tool • Function as the TMF process subject matter expert (SME...

View TMF Compliance Specialist Job - Raritan, NJ 08869
Trial Master File, TMF, eTMF, electronic TMF, electronic trial master file, compliance, compliant, clinical trial, audit, inspection, FDA, ICH/GCP, ICH, GCP, report, reporting, filing, file, archive, archival, archiving, external regulatory, regulatory
Clinical Outsourcing Manager
Science & Biotech - Berkeley Heights, NJ 08922

Clinical Solutions Group is partnering with an excellent sponsor company to find a talented Clinical Outsourcing Manager to join a growing team. This company has a great company culture and is located in the greater Plainfield, NJ area. Responsibilities will include, but are not limited to, the following: • Perform and manage all activities associated with the development and execution of contracts with Clinical Research Organizations performing clinical trial services and other vendors as necessary • Prepare study specific request for prop...

View Clinical Outsourcing Manager Job - Berkeley Heights, NJ 08922
outsourcing, clinical outsourcing, outsourcing manager, contracts, contract, Clinical Research Organization, CROs, vendor, vendors, RFP, RFPs, Request for Proposals, bidding negotiations, benchmark, benchmarking, sourcing strategy, negotiate, negotiations, negotiating, legal, study scope, scope of work, SOW, vendor performance, metrics, contract terms and conditions, terms and conditions, T&C, market analysis, market analysis, financial negotiations
Science & Biotech - Kalamazoo, MI 49001

The Sr. Clinical Research Associate (CRA) performs and coordinates all aspects of the clinical monitoring and site management process in accordance with ICH Good Clinical Practices, FDA guidelines, local regulations and Standard Operating Procedures. Conducts site visits to assess protocol and regulatory compliance and manages required documentation Responsible for ensuring that data will pass international quality assurance audits. Represents company in the global medical research community and develops and maintains collaborative relationships with ...

View Sr. CRA Job - Kalamazoo, MI 49001
sponsor, CRO, CRA, Regional CRA, Clinical Research Associate, independent monitoring, virology, oncology, Hep C, phase I, GCP, study sites, site management, SOP, regulatory compliance, clinical sites, study start up, start-up, site initiation, site visits, close-out, close out, HIV, Respiratory
Clinical Site Manager / In-House CRA
Science & Biotech - Wallingford, CT 06494

A highly reputable company in the greater New Haven area has a need for a Clinical Site Manager (In-House CRA). This opportunity office based and is initially a 12 month contract with the option to extend. This opening is targeting in-house CRAs with Site Management experience, Regional CRAs that wish to come in-house, and junior to mid-level Trials Managers with Site Management experience. Oncology and/or Neurology experience is desired, but not required. • Independently monitors the progress of assigned Investigative sites by maintaining c...

View Clinical Site Manager / In-House CRA Job - Wallingford, CT 06494
Clinical site manager, in-house CRA, in house CRA, iCRA, CRA, clinical research associate, ICH, GCP, ICH/GCP, FDA, guidelines, regulations, regulatory, protocol, site management, protocol management, site, clinical site, site issues, resolve, resolution, resolutions, timelines, project planning, investigative sites, site monitor, site monitors
Clinical Project Manager – Oncology - Remote / Home-Based
Science & Biotech - Salt Lake City, UT 84101

Clinical Solutions Group is currently partnering with an exceptional client for a Clinical Project Manager role. This position can be contact or contract to hire and it is 100% Remote. Candidates are allowed to work from their homes with minimal travel involved. Candidates for this opportunity MUST have prior monitoring experience and recent work in oncology. Candidates must also have worked on multiple studies and have both project management and people management. The Clinical Project Manager will manage single and full service clinical pro...

View Clinical Project Manager – Oncology - Remote / Home-Based Job - Salt Lake City, UT 84101
clinical trials, trials management, complex studies, outsourcing, difficult patient populations, large studies, phase III, large phase III studies, external vendor, outside vendor, service provider, initiation, close, closure, initiate, global, compliance, ICH, GCP, legal, regulatory, standards, SAE, serious adverse event, SAEs, Serious Adverse Events, risk, risk management, risks, Health Authorities, submission, submissions, ethics committee, ethics committees, investigator meeting, meetings, presentation, monitor training, supply, IMP, forecast, budget, financial plan, payment schedules, oversee, documentation, documents, time management, resolve issues, invoice, invoices, site payments, quality, review, Trial Master File
Sr. Safety Surveillance Associate
Science & Biotech - Carlsbad, CA 92010

The Sr. Safety Surveillance Associate will receive and analyze Serious Adverse Event (SAE) information for completeness, accuracy and regulatory reportability requirements; evaluate SAE case data with an emphasis on medical presentation, conduct discussions regarding specific patient case data with health care practitioners and Sponsors; determine regulatory reporting requirements based upon case data, product information, and FDA or ICH guidelines and regulations; prepare SAE Reports, including preparation of narrative summary; identify missing/discr...

View Sr. Safety Surveillance Associate Job - Carlsbad, CA 92010
SAE, AE, BSN, RN, data, queries, drug safety, pharmacovigilence, narrative summary, ICH, FDA, MedDRA
Central Labs Global Project Manager
Science & Biotech - Lancaster, PA 17602

Purpose: To deliver an industry superior sponsor-experience and project performance (time, quality/level of service and cost of awarded projects) that exceed the clients’ expectations and specifications. To oversee and coordinate all internal and external activities to ensure the smooth, timely and accurate flow of information required to meet the purpose of the role. To strengthen the client relationship and support business growth from repeat business. Key Accountabilities: • Consult and provide operational input into quotes / proposal ...

View Central Labs Global Project Manager Job - Lancaster, PA 17602
Central Laboratory, Global, operations, proposals, budgets, SOW, contract, Project Management, CRO, Sponsor, clinical research
Pharmaceutical Biostatistics Director
Science & Biotech - Irvine, CA 92618

Position Summary: The Director, Biostatistics will require experience in statistics, drug development, and clinical research. The Director, Biostatistics is expected to work collaboratively with the R&D department to determine accurate study designs, sample size estimates, and write sections of study protocols. Essential Job Functions: •Participate in study design and protocol development and ensure that study designs are consistent with study objectives and are optimal within study constraints. •Calculate sample sizes and/or...

View Pharmaceutical Biostatistics Director Job - Irvine, CA 92618
Biostatistics, SAS, Pharmaceutical, CRF Design, Database edit checks, Drug development
Pharmaceutical Clinical Data Manager
Science & Biotech - Irvine, CA 92618

Position Summary: The primary responsibilities of this position will be to coordinate clinical data management activities for phase I-IV clinical trials by supervising outside vendors and contractors, as well as performing data quality checks to ensure the integrity of the clinical data. Essential Job Functions: •Oversee clinical data management activities across multiple studies. Perform thorough reviews of critical CDM documentation such as eCRF specifications, eCRF completion guidelines, annotated CRFs, edit check specification...

View Pharmaceutical Clinical Data Manager Job - Irvine, CA 92618
Clinical Data Manager, EDC, eCRF, Oracle, GCP, CDISC, CDASH, SDTM, ADaM, SAS, SQL
Clinical Data Manager
Science & Biotech - Dallas/Fort Worth, TX 76134

Manage the creation, execution and maintenance of Data Management Plans in support of clinical study deliverables. Lead the design, creation and lifecycle management of data collection, validation and reporting specifications and usage guidelines. Support the training and development of certain CDM study personnel (e.g. Clinical Data Analyst I & II’s) through formal training and guided mentorship. Support the preparation of project budgets and financial reporting. Assist in the development of study resourcing plans and direct the activities ...

View Clinical Data Manager Job - Dallas/Fort Worth, TX 76134
Clinical Data Manager, Clinical Research, Pharma, Biotech, SAS, Biostatistician, Statistical Programmer, CDISC, ADaM, SDTM, EDC, Data Analyst, Data collection, Validation, Data Entry, Oracle Clinical, Medidata RAVE, InForm, Pharmacuetical, CRO, Clinical Research, CRA, Data Management
Director of Quality Assurance
Science & Biotech - San Diego, CA 91911

The Director of Quality Assurance reports to the President/CEO and provides leadership and management to the Quality Department in the development, implementation, administration, and documentation of our Quality Management System and its associated standards and systems to ensure that clinical trials are conducted and data is generated, documented, and reported in compliance with internal standards, GCP, ISO 9001 and relevant and applicable regulatory requirements. Perform duties in accordance with company’s values, policies, and procedures. Es...

View Director of Quality Assurance Job - San Diego, CA 91911
CAPA, Clinical Research, Biotech, Clinical Data, Research, Director, Quality Assurance, QA, GCP, ISO, Manager of Quality Assurance, Director of Quality Assurance, FDA, ICH, GCP,
Regional Clinical Research Associate - Houston
Science & Biotech - Houston, TX 77007

We are a large pharmaceutical sponsor. Preferred therapeutic areas are Oncology. Responsibilities • Perform designated projects in accordance with applicable SOPs, clinical on-site monitoring activities (drive patient recruitment, source data verification, drug accountability, data collection), collecting regulatory documentation (when required), performing qualification, initiation, monitoring and termination of investigational sites in accordance with ICH GCP guidelines. • Responsible for coordinating a moderate to large team or mult...

View Regional Clinical Research Associate - Houston Job - Houston, TX 77007
Regional CRA, Clinical Research Associate, GCP, ICH, Monitoring, Oncology
R&D Clinical Project Manager
Science & Biotech - Titusville, NJ 08560

Research and Development Clinical Project Manager Office Based in Titusville, NJ - some flexibility to work from home Long Term Contract! - BS Degree is required - 7 years of operational experience within the Pharma/ CRO industry - Align with the R&DC/sponsor clinical team on accurate planning of trials within program/project and ensure information is available to the team. -Own Request for Service (RFS), give operational input in design and implementation of the protocol. Provide Proposal for acceptance and execution of a clinical trial by ...

View R&D Clinical Project Manager Job - Titusville, NJ 08560
Research and Development, R&D, RFP, Management, RFS, Operational, Clinical Project lead, CPL, CPM, Project manager, global trial, outsourcing
SQL Developer
Other - Palm City, FL 34490

This position is for a temporary/contract resource to develop database application for corrective action system. Effort will replace existing FileMaker Pro Database application and develop interface into existing ERP system. Position will report to VP of Process, Quality to specify application requirements, develop application, debug, pilot, and provide documentation and training. ESSENTIAL FUNCTIONS 1. Responsible for the development and configuration of databases and database interfaces in the organization. The role includes the development and...

View SQL Developer Job - Palm City, FL 34490
sql, database, developer, configuration, vba, microsoft, palm city, stuart, florida
SQL Developer
Information Technology - Palm City, FL 34990

This position is for a temporary/contract resource to develop database application for corrective action system. Effort will replace existing FileMaker Pro Database application and develop interface into existing ERP system. Position will report to VP of Process, Quality to specify application requirements, develop application, debug, pilot, and provide documentation and training. ESSENTIAL FUNCTIONS 1. Responsible for the development and configuration of databases and database interfaces in the organization. The role includes the development and...

View SQL Developer Job - Palm City, FL 34990
SQL, developer,
Director of Clinical Affairs
Science & Biotech - San Jose, CA 95101

Requirements: • Bachelor’s degree in a science/health related field including a minimum of 5 years in management. • 10 years clinical research experience in medical device, pharmaceutical or biotechnology is required. • Advanced degree (M.S., Ph.D, MD) is preferred • Familiarity/experience with US and foreign clinical trial requirements, global experience preferred • Previous experience selecting and initiating and monitoring clinical research sites • Excellent...

View Director of Clinical Affairs Job - San Jose, CA 95101
clinical research, clinical affairs, device, Director
Director of QA
Science & Biotech - Chula Vista, CA 91909

Education/Experience: Bachelor's degree (B.A.) from a four-year college or university in Life Sciences or related field with 10+ years Quality Assurance Management experience, 5+ at Director level required, 5+ Early Phase Clinical trial management and/or QA experience, and 2+ ISO 9001 experience. Deep knowledge of and experience with GCP is an absolute must. Skills, Knowledge, and Abilities: Advanced knowledge of US and International Regulatory requirements for clinical research including FDA/ICH-GCP; knowledge of ISO 9001;demonstrated leadership...

View Director of QA Job - Chula Vista, CA 91909
iso 90001, gcp, QA, quality assurance, fda, ich
Process Engineer
Manufacturing & Production - Decherd , TN 37324

Process Engineer Location: Decherd, TN Major Responsibilities will include but not limited to: new model development, current model development, new equipment specification development, installation and startup; developing, implementing, and monitoring supplier quality systems through standards: SPC, FMEA, and control plans. The central purpose of all of these duties is to assist the Decherd Powertrain plant in achieving quality, cost, delivery, and safety goals. Qualifications and Requirement: B.S. Degree in Engineering from an ...

View Process Engineer Job - Decherd , TN 37324
Automotive, Industrial, Manufacturing, Process Engineer,
Permanent - Sr. SAS Programmer
Science & Biotech - Watertown, MA 02471

Responsibilities: • Design, develop, evaluate, validate and modify computer programs using SAS to analyze and evaluate clinical data • Produce and deliver standard datasets, program edit checks and produce quality tables, figures and listings in a timely fashion and high quality • Possess thorough knowledge of CDISC theory and implementation guidelines, able to create and validate CDISC standard datasets • Provide expertise in the design and development of clinical trials, protocols, case report forms and clinical databases • W...

View Permanent - Sr. SAS Programmer Job - Watertown, MA 02471
SAS, Clinical, Research, Pharmaceutical, Biotechnology, Programming
Technical Recruiter
Information Technology - Fremont, , CA 94539

What we’re looking for? Oxford's continued success is attributed to the success of our employees. We hire the best and the brightest. We've developed programs and created tools designed to effectively accelerate your career. As you achieve, we want to make sure you are rewarded not only financially, but also with opportunities for advancement. Nearly 95 percent of all managers are promoted from within our organization. To learn more about this opportunity, contact us now or attend Oxford’s virtual career fair, where one of our Staff Recruiters w...

View Technical Recruiter Job - Fremont, , CA 94539
Sr. Clinical Research Associate
Science & Biotech - Houston, TX

DOCS Global is actively seeking Clinical Research Associates (CRAII), Regional, in Houston. Experience working with multiple protocols is required. Experience facilitating pre-study initiation process, orienting site personnel on protocols and procedures, compliance to FDA Regulations and managing site activities is a must. Must have BA/BS/BSc plus a minimum of 3+ years experience in the pharmaceutical or biotech industry. Role Highlights In addition to a competitive package, we are offering CRAs long-term contract roles with DOCS and the ch...

View Sr. Clinical Research Associate Job - Houston, TX
local travel, monitoring, oncology, multiple protocols, contract
Senior Biostatistician
Science & Biotech - San Francisco, CA 00000

About The Opportunity: Our client is looking for a Senior Biostatistician to join their growing Biometrics group. The preferred candidate will have experience in the pharmaceutical or biotech environment. This individual must bring experience in the analysis and reporting of clinical study data to both internal stakeholders as well as to external audiences. Ideally, this experience would include exposure to the design, analysis and reporting of clinical studies in late stage clinical development. The Senior Biostatistician will support the de...

View Senior Biostatistician Job - San Francisco, CA 00000
SAP, CRF, Statistics, Statistician, Clinical, SAS, Pharmaceutical, Biotech, Phase, Trial
Data Management SAS Programmer
Science & Biotech - Wayne, PA 19087

About The Opportunity: Our client is a biopharmaceutical company based in the greater Philadelphia, PA area. They have an impressive team of highly experienced scientists and pharmaceutical professionals collaborating across discovery, development and commercialization. The Database Programmer is responsible for producing reports for use by the Clinical Data Managers. This individual will develop transfer specifications with vendors for external data sources, performing Study Data Tabulation Model (SDTM) conversion dataset programming and Quality ...

View Data Management SAS Programmer Job - Wayne, PA 19087
SDTM, SAS, Database, Program, Programmer, Data, Conversion, Oracle, CDISC
Clinical Outsourcing Consultant
Research - Woodcliff Lake, NJ 07677

Support internal customers in the development of outsourcing requirements for Phase I-IV global clinical trials. Lead and support the qualification and evaluation process for new service providers. Lead the process of Request for Proposal (RFP) development from service provider selection through final contract execution. Manage the contracting process including preparation, finalization, and administration of CDAs, MSAs, Service Agreements, Work Orders, Change Orders, and Amendments. Coordinate development of service requirements, e.g., statement-...

View Clinical Outsourcing Consultant Job - Woodcliff Lake, NJ 07677
outsourcing, contracts, budget, clinical trials, phase I-IV, service agreements, MSA
Senior Internal Auditor - Banking/Financial Services
Other - Chicago, IL 60601

Immediate need for a Dynamic Senior Internal Auditor for our financial services client located in the Chicago Loop. This is an exciting opportunity to participate in the amazing growth taking place within this organization, join a highly motivated team and develop as a professional, potentially leading to other positions in the organization. The Senior Auditor will perform complex professional internal auditing work. Work involves leading or participating in audit projects, providing consulting services to the organizations management and staff, a...

View Senior Internal Auditor - Banking/Financial Services Job - Chicago, IL 60601
CPA, CIA, internal audit, banking, financial services
Transportation Rate Analyst
Manufacturing & Production - Phoenix, AZ 85018

Growing manufacturing company headquartered in Phoenix is looking to add a Transportation Rate Analyst to provide safe and cost effective analysis for transportation shipments with focus on rail, highway, and marine. Essential Job Functions Negotiate rates as needed with contract carriers. Provide analysis of current transportation and operations practices to determine process and cost improvement opportunities. Provide the necessary freight analysis and decision support systems for other functional areas. Develop, format and distribute mo...

View Transportation Rate Analyst Job - Phoenix, AZ 85018
Tranportation, Rates, SAP, Rail, highway, marine, barge, containers
Clinical Research Associate (In-House)
Science & Biotech - Redwood City, CA 94061

DOCS Global is seeking experienced CRAs for an in-house position with a growing client in Redwood City. Qualified candidates will monitor the initiation and performance of clinical trials at external research sites to assure compliance with all study procedures and regulatory requirements. Serve as the primary liaison with the research site, track the progress of the study and resolve problems with the study execution. Assist with the development of study protocols, and identifies potential research sites. 3-5 years experience in a CRA role. Car...

View Clinical Research Associate (In-House) Job - Redwood City, CA 94061
Clinical Research Associate, CRA, monitor, Cardiovascular, device, in-house, in house, clinical trial, clinical study, study start up, site, clinical research
Senior Managing Consultant - Merger, Acquisition, Divestiture and Joint Venture
Management & Business - Teaneck, NJ 07666

MERGER, ACQUISITION, DIVESTITURE AND JOINT VENTURE SENIOR MANAGER Job Description We are looking for highly motivated and ambitious merger, acquisition, divestiture and/or joint venture experienced professionals across several levels (Senior Consultant, Manager, Senior Manager and Director) with a proven track record of engagement leadership and execution and who will bring to bear their industry, strategy, skills, and process expertise to deliver significant impact to our clients and practice. Our Mergers & Integrations practice helps clients...

View Senior Managing Consultant - Merger, Acquisition, Divestiture and Joint Venture Job - Teaneck, NJ 07666
Regional Clinical Research Associate - Los Angeles
Science & Biotech - Los Angeles, CA 90210

We are a large pharmaceutical sponsor. Preferred therapeutic areas are Oncology and Cardiology. Responsibilities • Perform designated projects in accordance with applicable SOPs, clinical on-site monitoring activities (drive patient recruitment, source data verification, drug accountability, data collection), collecting regulatory documentation (when required), performing qualification, initiation, monitoring and termination of investigational sites in accordance with ICH GCP guidelines. • Responsible for coordinating a moderate to lar...

View Regional Clinical Research Associate - Los Angeles Job - Los Angeles, CA 90210
Regional CRA, Clinical Research Associate, GCP, ICH, Monitoring, Oncology, Cardiology
Engineering Manager
Engineering & Architecture - Puyallup, WA 98371

Engineering Manager Direct Hire Location: Puyallup, WA Pay: DOE Job Goals: Under the general supervision of the Plant Manager, the Engineering Manager is responsible for coordinating design changes and engineering support for the manufacturing operation. This includes the development and leadership of all Engineering, CNC Programing, Tooling and Maintenance personnel to support all building, facility operations and process engineering activities. This position is also responsible for creating and managing complex capital projects, assis...

View Engineering Manager Job - Puyallup, WA 98371
ISO/AS9100, ISO14001, Lean Manufacturing, Engineering, Manager, CNC, six sigma
Project Engineer
Information Technology - Boca Raton, FL 33432

JOB SUMMARY The person(s) in this position will work as a team member or team lead for design, implementation, documentation and handoff of IT projects. These projects range in size from single server installations to multi-server, multi-site installations and utilize a wide range of technologies, including Microsoft, Cisco, HP, Dell, VMWare, Juniper, and various other Tier-1 vendor products. This position will work as a member of the sales and technical teams providing design and development of the project’s architecture, Project Schedules, Project...

View Project Engineer Job - Boca Raton, FL 33432
customer, troubleshooting, projects, engineer, server, installation
Sr. QA Auditor (GCP)
Science & Biotech - Houston, TX 77001

Candidate will be responsible for the following: •Enhance worldwide clinical quality assurance programs and audit ongoing studies, systems and documents to assure quality assurance compliance with regard to all regulatory guidelines, acting in a Management role and providing updates regularly. •Routinely provide GCP/QA consultation for all Company staff; assist in review of group SOP’s; assist in sponsor audits/inspections. •Ensure the timely and effective follow up of all identified or assigned quality issues. •Keep up-to-date with rele...

View Sr. QA Auditor (GCP) Job - Houston, TX 77001
GCP, QA, Auditing
Sr. QA Auditor (GCP)
Science & Biotech - Plainsboro, NJ 08536

Candidate will be responsible for the following: •Enhance worldwide clinical quality assurance programs and audit ongoing studies, systems and documents to assure quality assurance compliance with regard to all regulatory guidelines, acting in a Management role and providing updates regularly. •Routinely provide GCP/QA consultation for all Company staff; assist in review of group SOP’s; assist in sponsor audits/inspections. •Ensure the timely and effective follow up of all identified or assigned quality issues. •Keep up-to-date with rele...

View Sr. QA Auditor (GCP) Job - Plainsboro, NJ 08536
GCP, QA, Auditing
Field Medical Manager
Science & Biotech - Plainsboro, NJ 08536

Description: Position supports the function of Field Medical working both within a therapeutic area(s) and with impact across the function of Field Medical to support the safe and appropriate use of company medicines. Responsibilities include: Provide assistance in the development of National Field Medical and Thought Leaders plans and collaborates with Associate Director (AD) on the development of regional aligned plans. Ability to handle project work streams and initiatives aligned with the Medical Plan to deliver impactful HCP interactions. Deve...

View Field Medical Manager Job - Plainsboro, NJ 08536
MSL, field manager, stakeholder communications, project management
Actuarial Consulting Office Receptionist
Healthcare & Medical - Lebanon, TN 37087

Medical recruiting office in need of a receptionist. Please call 615-547-6396. Salary is negotiable depending on experience (Monday-Thursday 9am to 2pm/Fridays 9am to 12pm) IMMEDIATE OPENING!

View Actuarial Consulting Office Receptionist Job - Lebanon, TN 37087
Secretary, entry level
Project Engineer/Mechanical Enginee
Engineering & Architecture - Seattle, WA 98108

Medical equipment manufacturing company in Seattle is seeking a Project Engineer/Mechanical Engineer. Looking for a self-starter responsible for the planning, development, and release to manufacturing of new product projects and for the planning, execution, and release of updates to existing products. Primary objective is to deliver projects on schedule, within project budget, meeting all technical requirements, and within product COG target. Location: Seattle, WA Pay: Competitive Duration: Temp-hire Shift: 1st ESSENTIAL DUTIES AND RESPON...

View Project Engineer/Mechanical Enginee Job - Seattle, WA 98108
medical device, Project Engineer, Mechanical Engineer, ISO, FDA
Dynamics AX Administrator
Information Technology - Boulder, CO 80301

Blue Line Talent is seeking a mid to senior level Microsoft Dynamics AX administrator with notable work experience in AX 2012 for this contract position in downtown Boulder. We seek an accomplished Dynamics AX Administrator who enjoys a hands-on technical task leadership role in a highly collaborative and dynamic small team environment. Job Title: Dynamics AX 2012 r2 ERP System Application Administrator (contract) Work Location: Downtown Boulder The Client: • Publicly traded, Colorado-based, start-up Position Details: • Fie...

View Dynamics AX Administrator Job - Boulder, CO 80301
Systems Administration, System Administor, Microsoft Dynamics AX 2012, Management Reporter, AOT, X++ coding, SQL Server, ERP System Application Administrator, Xpo
Senior QA Tester Lead
Other - Minneapolis, MN 55419

Our client is looking for a Senior QA Tester on a 6+ month contract basis Coordinates changes with developers, technical writers and end users, Develops and performs test model validation, Implements software testing methodologies ,Performs unit, integration and/or regression testing 12+ years of testing experience. • Within 12 years, Should have been in test manager role for at least 4 years. • Should have handled testing of 1 or 2 mobile applications testing. • Strong test management experience is expected....

View Senior QA Tester Lead Job - Minneapolis, MN 55419
mobile testing, automated testing
Inside Sale Representative
Sales & Sales Management - San Diego , CA 92101

Who is encouraged to apply? - Candidates with Restaurant/Hospitality/Retail Management backgrounds looking to make a transition to sales. - Sports-minded individuals with competitive drive. - Recent Grads with strong track record of performance. was recently named #673 on the Inc. 5000 Fastest Growing Companies in America & 6th Fastest Growing Company in San Diego by San Diego Business Journal. As we continue to expand at a rapid pace, alternative career paths and special assignments will arise, giving YOU the opportunity t...

View Inside Sale Representative Job - San Diego , CA 92101
sales, account manager, inside sales, b2b, b2c, outside sales, account executive, sales reps
Technical Support Analyst
Other - Minneapolis, MN 55401

Our client is looking to add an additional Technical Support Team. They do require a undergrad degree. After completing their comprehensive training program, you will be working either 1st or 2nd shift. Resolve client tech issues Determine effective resolution of issues by troubleshooting & analyzing computer system errors of moderate to difficult scope where analysis of situations or data require an in-depth eval Provide remote tech support for hardware (printers, desktop, laptop, drivers, monitors, and PDAs) & software (internally developed app...

View Technical Support Analyst Job - Minneapolis, MN 55401
technical support, customer service,
Software Engineer - REST, Groovy, Java, TDD
Other - Minneapolis, MN 55419

Looking for experience software engineer to join our client's highly collaborative team of engineers, builders and problem solvers that share an open lab environment. This team is committed to code simplicity and consistent high quality. Responsibilities: • Collaboration with team members and others to define and understand software requirements and design. • High quality software development and delivery. • Tier three application support in test systems and production. Skills: • At least five years of relevant systems software en...

View Software Engineer - REST, Groovy, Java, TDD Job - Minneapolis, MN 55419
REST, HTTP, Groovy, Spring, XML, Agile
Solutions Engineer - Delivery
Information Technology - St Louis, MO 63115

Solutions Engineer Datalink has a clear vision for growth, a penchant for successful execution, and a robust, comprehensive portfolio of data center services and solutions. We enable our customers to transform their data centers to become more efficient, manageable, and responsive to evolving business demands. Datalink successfully delivers projects that provide business agility and cost efficiency while strengthening business and IT alignment. Doing so demands exceptional talent from our workforce. We support and nurture our talented team, w...

View Solutions Engineer - Delivery Job - St Louis, MO 63115
Delivery, Post Sales, Engineer, Architect, Implement, Services