Biotech Research Lab Jobs

470 jobs

Seeking a CRN who will coordinate the conduct of Phase I – IV clinical trials including consenting, screening and enrolling eligible subjects, managing subject treatment per protocol, oversight and coordination of research testing, including labs, office visits and radiology exams, provide oversight for research medication administration, monitor patient care, treatment side effects and patient st...

Position SummaryAssists in the management of the clinical monitoring process to ensure site adherence to applicable regulatory requirements, ICH/GCP Guidelines, company SOPs, and study protocols.Ensures coordination of an accelerated study start-up including pre-study visits, initiation, interim, and closeout activities associated with clinical trials to ensure timelines and metrics are met and ma...

Serves as primary contact point between the sponsor and the investigational site. A Site Manager is assigned to trial sites ensuring inspection readiness through compliance with the clinical research protocol, company's Standard Operating Procedures (SOP), codes of Good Clinical Practice (GCP), applicable regulations and guidelines from start-up through data-base lock. Responsibilities include sit...

Serves as primary contact point between the sponsor and the investigational site. A Site Manager is assigned to trial sites ensuring inspection readiness through compliance with the clinical research protocol, company's Standard Operating Procedures (SOP), codes of Good Clinical Practice (GCP), applicable regulations and guidelines from start-up through data-base lock. Responsibilities include sit...

This is a 5 month contract that could go longer, but not certain at this time. Surgical study. In house. Must have 4-6 years as an In House CRA, management of CRO and other vendors, exp reviewing Trip Reports, TMF oversight and general management of CROs and Monitoring teams. Position Summary Assists in the management of the clinical monitoring process to ensure site adherence to applicable regu...

- Assists with the management and development of study related documents including clinical protocols, case report forms, study manuals, and other study related tools. - Reviews and approves site activation documentation - Participates in site qualification and site initiation process, including scheduling of monitor activities with site personnel. - Assists in planning and preparing materials ...

With 30 years of experience in the CRO/pharma industry and more than 13,000 employees worldwide, PPD's lab services units continue to flourish. PPD continues to recognize our employees as the cornerstone of our success and strive to provide a supportive environment that offers exciting opportunities for skills enhancement. Our cutting-edge technologies, real time analytics and superior training dr...

We are seeking an experienced Clinical Data Project Manager. This is a full time position available in our office in Research Triangle Park (NC).Primary Goals:? Responsible for all data deliveries for assigned projects within time and budget with highest priority applied to data quality.? Responsible for the planning, organization, and coordination of Data Management & Systems, Statistics and Medi...

We are seeking an experienced Clinical Data Project Manager. This is a full time position available in our office in Research Triangle Park (NC).Primary Goals:· Responsible for all data deliveries for assigned projects within time and budget with highest priority applied to data quality.· Responsible for the planning, organization, and coordination of Data Management & Systems, Statistics and Medi...

Job summary The Clinical Site Manager (CSM) is primary point of contact with all clinical sites during clinical trials. As such, the CSM is responsible for providing technical, educational and clinical support to their assigned sites for our clinical research studies. The CSM is responsible for overseeing or managing all aspects of the studies relating to clinical site screening and recruitment,...

Serves as primary contact point between the sponsor and the investigational site. A Site Manager is assigned to trial sites ensuring inspection readiness through compliance with the clinical research protocol, company's Standard Operating Procedures (SOP), codes of Good Clinical Practice (GCP), applicable regulations and guidelines from start-up through data-base lock. Responsibilities include sit...

Serves as primary contact point between the sponsor and the investigational site. A Site Manager is assigned to trial sites ensuring inspection readiness through compliance with the clinical research protocol, company's Standard Operating Procedures (SOP), codes of Good Clinical Practice (GCP), applicable regulations and guidelines from start-up through data-base lock. Responsibilities include sit...

Major Duties and Responsibilities: Research Associate (RA) will work in a collaborative setting with other cell line and cell culture development staff on CMC development projects. RA’s primary responsibility is to support recombinant cell line and cell culture development. This will include recombinant protein productions, maintaining clinical and research cell lines, solution and cell culture m...

My name is Jon Foster and I am a VP/ Recruiter at Staff Icons. I am reaching out to you to inform you, your friends, or colleagues of a NEW Lab Director, Cytogenetics job opportunity located in Seattle, WA area. If interested, please send me your resume/referral info. See additional info below: Job Summary We are looking for a Director of Cytogenetics in the Seattle WA area. ABMG Boarded in C...

TechData is looking for Outcome research statistician(Econometrician, Economic Modeler), Biostatistician, Pharmacovigilance Physician Physician, Pharmacovigilance Scientist, SAS Programmer/Statistical Programmer (Some can be telecommuting), Hadoop Administrator, Sr. Clinical Data Manager, Drug Safety Specialist, Clinical Research Assoc IIIfor our pharmaceutical clients in Central NJ. Please see be...

Applied Research Scientist – Molecular Biology Enfold is a private biotech company dedicated to creating the next generation of molecular biology cloning and expression systems for both eukaryotic and mammalian platforms. We are looking for creative, inventive, and talented Molecular Biologists who enjoy working collaboratively. The position will involve periods of sustained literature research, ...

Job Title: Bioinformatician/Research IT Specialist Location: Cambridge, Massachusetts Job Description: *LOOKING FOR 4-5 YEARS OF EXPERIENCE IN BIOLOGY FOCUSED LABS. The IT department for BioMedical Research (NIBR) is looking for a degree-educated Bioinformatician/Research IT Specialist with an excellent understanding of biology, research data, and lab workflows, as well as experience in softwa...

Company Confidential
Summary Opportunity to work full time in an exciting and growing biotech company as a Research Laboratory Technical Specialist. The position offers flexible hours and opportunities to work with leading universities and experts on a variety of projects to develop advanced medical technologies. Major Responsibilities: Follow established protocols to perform biological tests and assays. Develop a...

Zhejiang Hisun Pharmaceutical Co. Ltd. was established in 1956 and currently employs over 7000 people, and is a public trade company (stock code 600267). Hisun’s vision is to become a widely respected international pharmaceutical company by advancing its mission of persisting in pharmaceutical innovation for the benefit of human beings.Hisun focuses on the integration of pharmaceutical research an...

Lab Tech/ Animal Care /Full Time Lab Tech / Animal Care ACT We are looking for Laboratory Technicians (Animal Care Technicians) for an international biotech company in Rensselaer. These positions are TEMP with a possibility of Temp to Hire for the right candidate. These positions are 40 hours / week, M-F. This company is the leader in producing laboratory mice for pharmaceutical research and deve...