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Biotech Research Lab Jobs

546 jobs

Serves as primary contact point between the CRO, sponsor and investigational sites.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 site selection, pre-...

Scientist, Process Research & Development Thriving pharmaceutical company is looking for a talented organic chemist to join a process R&D group as a scientist. You will be responsible for: •Developing, optimizing and implement synthetic processes •Managing process development and scale-up activities (for early to mid-stage drug candidates) •Working with small molecule drugs substances •Worki...

Serves as primary contact point between the CRO. sponsor and investigational sites. 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 s...

Serves as primary contact point between the sponsor and investigational sites. 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 site s...

Responsibilities The ideal candidate will use his/her extensive sales knowledge and experience to perform a variety of business management, analytical, and support functions including the following activities: • Executing outbound calls to customers using professional selling skills to generate and close a high number of quality leads and quotes. • In-depth knowledge of all internal operations ...

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 Medical Writing activities in a set of projects belonging to one or more clients; such that quality, timelines and budget meet expectations.? Respons...

Manufacturing Technician - Biotech, La Jolla, CA Kelly Scientific Resources, a division of Kelly Services, is currently seekingseveral, 2nd shift Manufacturing Technicianswork with a fast-growing scientific/technology company focusedon using modified/synthetically produced microorganisms to produce alternative fuels located in La Jolla, CA. Position Type: Contract Work schedule/Shift: 2nd shift...

Serves as primary contact point between the sponsor and investigational sites.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 site selection, pre-trial...

Entry Level positions in Biotech (Germantown) We are reviewing resumes for a variety of ENTRY level (and experienced) positions for a Biotech firm in Germantown, NY, (off 9G, just south of Hudson and 40 miles north of Poughkeepsie). These are lab tech animal care positions requiring dedicated and motivated individuals who are ready for a new career opportunity. Training and career development is...

Serves as primary contact point between the CRO. sponsor and investigational sites. 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 s...

Serves as primary contact point between the CRO, sponsor and investigational sites.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 site selection, pre-...

Job Description / Capsule Develops procurement partnerships with key business stakeholders in the MedImmune Biologics operating unit in support of all preclinical service categories. Leading demand and supply side activities, this role has 4 major types of accountability: * Strategic relationship management - to ensure that Category Strategies are highly aligned to current and future Business nee...

Serves as primary contact point between the sponsor and investigational sites.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 site selection, pre-trial...

Job Description / Capsule Develops procurement partnerships with key business stakeholders in the MedImmune Biologics operating unit in support of all preclinical service categories. Leading demand and supply side activities, this role has 4 major types of accountability: * Strategic relationship management - to ensure that Category Strategies are highly aligned to current and future Business ne...

Serves as primary contact point between the CRO. sponsor and investigational sites. 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 s...

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,...

Summary: •The job holder is accountable for the quality of work performed. •Independently perform all work to satisfy DM Management, DPM and Sponsors. •Responsible for ensuring the completion of multiple Data Management projects according to sponsor and contract requirements and in accordance with applicable standard operating procedures.•Study lead for Data Project Manager and as appropriate w...

Job Title: Clinical Data Manager (2 openings) Working Arrangement:Onsite at large pharma in Northern NJ Initial Duration:6 months with the option to be extended Duties: Responsible for providing timely and professional ongoing quality management of clinical trial data by identifying errors/inconsistencies in CRF data and ensuring their resolutions in order that databases can be declared clean a...

BioClinica is the worldwide leader for medical imaging core lab services, providing pharmaceutical, biotech, and medical device companies with clinical trial support for all phases and across all major indications. The PET Research Specialist performs image collection, quality assurance and both quantitative and qualitative analysis of phantom and patient PET or SPECT data acquired in the context...

BioClinica is the worldwide leader for medical imaging core lab services, providing pharmaceutical, biotech, and medical device companies with clinical trial support for all phases and across all major indications. The PET Research Specialist performs image collection, quality assurance and both quantitative and qualitative analysis of phantom and patient PET or SPECT data acquired in the context...