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FULL-TIME Director, DOCS Program Management -Statistical Programming
Research - Lawerenceville, NJ 08648

Roles & Responsibilities of the Position The responsibilities of the Operations Manager include, but are not limited to: CPC MANAGEMENT • Complete DOCS induction and orientation for newly employed CPCs. • Ensure client-specific induction and orientation is planned, communicated and completed. • Establish goals and objectives for each CPC. • Monitor performance and conduct annual appraisal for each CPC, as applicable. • Conduct regular 1:1 meetings with assigned CPCs. • Ensure timely submission and approval of time reports, expense reports ...

View FULL-TIME Director, DOCS Program Management -Statistical Programming Job - Lawerenceville, NJ 08648
Entry Level Animal Care Technician
Research - Indianapolis, IN 46241

Contract Length: 90-days Temp-to-Perm Hours: • Normal (8) hour days, Monday – Friday. • Start times are varied depending upon location. For example if start time is 7:00am their day would end around 3:00pm. If start time was 9:00am their day would wrap up around 5:00pm. FYI - 9:00am is the latest start time. • Once the schedule has been determined, it will not change. It will be consistent week to week. Key Points- this is not a job for everyone • Handling mice and rats that are genetically bred for medical testing • They will be cleaning cag...

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Clinical Logistics Associate
Research - Tarrytown, NY 10533

Responsibilities • Manages and tracks investigational product (IP) inventory; advises supply management team of potential shortages and makes recommendations for resupply activities based on usage trends. • Initiates IP shipment orders according to supply plans or as requested by Clinical Trial Management team; tracks orders through receipt at investigator study sites; communicates with distribution vendors to ensure timely and compliant shipment and delivery to investigator sites. • Reviews and evaluates temperature excursion data and communica...

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Director of Clinical Research Protection
Research - Los Angeles area, CA 91008

The Research Protections is responsible for the review and oversight of all human subject research conducted. The Director for Clinical Research Protections assures and maintains compliance with federal and state regulatory requirements for the conduct of research as well as prepares AAHRPP (Association for the Accreditation of Human Research Potection Programs) applications and maintains accreditation. The Director for Clinical Research Protections, reports to the Senior Director, Research Protections The Director for Clinical Research Protections i...

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Regulatory Affairs Coordinator
Research - Los Angeles area, CA 91008

Regulatory Affairs Coordinator Position Summary and Key Responsibilities: Will be responsible for all aspects of clinical research regulatory compliance, including document preparation, submission, and management, for a specified portfolio of clinical trials. Essential Functions: • Coordinate the preparation and timely submission of regulatory documents Institutional Review Board (IRB), Cancer Protocol Review and Monitoring Committee (CPRMC), Data Safety and Monitoring Board (DSMB), other internal committees, national cooperative groups, industr...

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regulatory affairs
Sr Director Clnical Research IVD
Research - Boston, MA 02453

-Sr Director will report to the VP of Quality and Regulatory. Team to be supervised is 11 Clinical Study Managers (5 in Finland, 3 in China and 3 in US) - Requirements: - Ph.d preferred but MS will be considered. MD Degrees in other related scientific fields besides Biochem and Molecular will also be considers. - 7+ years’ experience clinical experience in Medical Device or Pharma and including leadership - Past success in designing/developing clinical studies - Well-polished communicator and experience interfacing with regulators a...

View Sr Director Clnical Research IVD Job - Boston, MA 02453
Regulatory CMC Manager
Research - Freemont, CA 94555

The manager reports to the Director of Regulatory Affairs, this position will be responsible for contributing to proactively managing CMC aspects of one of more global clinical programs including overseeing preparation and submission of global CMC submissions, ensuring the CMC content is complete, well-written and meets all relevant requirements. This position will contribute to the evaluation of proposed manufacturing changes for regulatory impact to ongoing and existing filings and providing strategic regulatory guidance for optimal implementation o...

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Clinical Sample Processor I
Research - Farmingdale, NY 11735

Looking for an individual to process a backlog of samples and get them in to the correct storages areas. HS degree required as is Reliable Transportation. This person will be required to work even in inclement weather as the department never closes.

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Medical Technologist
Research - Farmingdale, NY 11735

• *Responsible for the quality and timelines of technical procedures, as well as their compliance with applicable company, CAP, and local regulatory agency testing requirements. • *Perform technical assignments and testing and issue reports in accordance with written procedures. These should be processed within agreed turnaround times. • *Enters and releases required information in the LIS, such as test results, comments, and quality control results in a timely manner with compliance to all regulatory requirements. • *Adheres to written internal ...

View Medical Technologist Job - Farmingdale, NY 11735
CHIEF ECONOMIST and HEAD OF ECONOMIC RESEARCH CENTER
Research - LOS ANGELES , CA 90071

CHIEF ECONOMIST and HEAD OF ECONOMIC RESEARCH CENTER Our client is a well-established, prestigious Los Angeles economic development leadership organization that promotes a globally competitive, prosperous and growing LA County economy. They are seeking an experienced, talented Regional Economist with a PhD in Economics, to fill a high-profile position heading up their key economic research Center in Los Angeles County and surrounding areas in Southern California which encompasses the Southern California region, including the counties of Los Angele...

View CHIEF ECONOMIST and HEAD OF ECONOMIC RESEARCH CENTER Job - LOS ANGELES , CA 90071
Ph.D., economic analysis, forecasting, media relations, Spanish, labor economics. development economics, public policy, Los Angeles
Senior Clinical Project Manager-HOMEBASED in MASSACHUSETTS
Research - Boston, MA 02134

This position can be home based ANYWHERE in MASSACHUSETTS! Our client is currently hiring a SENIOR CLINICAL PROJECT MANAGER, home based. Global experience is preferred. Excellent team looking for someone with good leadership skills, as well as strong clinical research knowledge and understanding. Excellent communication skills necessary. 4+ years of project management experience is preferred as well as prior CRO experience. Ideal would include both CRO and sponsor experience. Job Summary (including but not limited to): Provide leaders...

View Senior Clinical Project Manager-HOMEBASED in MASSACHUSETTS Job - Boston, MA 02134
clinical operations, CRA manager, clin ops, clinical research, project management, trial management, global trials
Sr. Contracts and Grants Analyst
Research - NEW YORK, CA 100007

Summary: Responsible for the development and analysis of contractual relationships including investigator grants including but not limited to drafting, negotiating, and finalizing agreements related to clinical trials. Provide support to the clinical team in the pricing, planning, execution and control of grants and contracts. Principal Responsibilities: Responsible for analyzing contract requests/needs from operating companies and translating into appropriate contracts/budgets for company sponsored and investigator initiated clinical tr...

View Sr. Contracts and Grants Analyst Job - NEW YORK, CA 100007
Contracts Analysts, Contracts Specialists, Contracts Administrators, Contracts Negotiators, Contracts Managers
Clinical Research Associate
Research - CANADA , TN 00000

Job Title: Clinical Research Associate Experience: 3+ years Therapeutic areas:Oncology Location: Canada Roles & Responsibilities of the position PRINCIPAL RESPONSIBILITIES: - Participates in site feasibility and/or pre-trial site assessment visits, providing recommendation from local area about site/investigator selection in collaboration with the trial team - Acts as primary local company contact for assigned sites for specific trials. - Attends/participates in investigator meetings as needed. - Responsible for executing activities...

View Clinical Research Associate Job - CANADA , TN 00000
CRA,"clinical research associate",Oncology
Home Based Regional CRA (Oncology, Cardiovascular, or Neuroscience)
Research - regional, PA 19454

Multiple Home Based Regional Clinical Research Associate positions available for individuals who live in or are located within a commutable distance to a major city. Opportunities available located in the following areas: Los Angeles and San Francisco, CA; North East Region (NY, NJ, PA, DC-MD, MA area); Chicago, IL and the Pacific North West. Qualified candidates must demonstrate a minimum of 3 years CRO or Pharmaceutical company clinical research on-site monitoring experience. Individuals with experience monitoring Oncology; Neuroscience, Cardiovasc...

View Home Based Regional CRA (Oncology, Cardiovascular, or Neuroscience) Job - regional, PA 19454
Regional CRA; CRA; Clinical Research Associate; Clinical Trials