Clinical Trial Jobs in Cambridge
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Search Results - Clinical Trial Jobs in Cambridge
Simcere Zaiming-Cambridge
to improving the lives of patients in China and worldwide. Our culture values sincerity, collaboration, result orientation, and a relentless pursuit of scientific excellence.
Position Overview:
We are seeking an experienced and detail-oriented Clinical Trial...
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SPECTRAFORCE-Cambridge
biospecimens in clinical trials or research settings.
• Biospecimen Management & Lab Coordination requires end-to-end workflow coordination, timeline planning and milestone tracking, strong biospecimen lifecycle expertise, clinical trial systems & tools...
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Beacon Hill-Cambridge
Job Description
Job Title: Clinical Trial Associate
Contract Term: 6 months to start; could extend
Hybrid - 3 days onsite required in Cambridge
Experience required:
Sponsor exp is REQUIRED
Preferred Qualifications
Project Coordination...
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Arroyo Media-Cambridge
to complete your profile to be considered for participation. Once complete, invitations will reach you via on-site or via email.
• Compensation various per difficulty and length of study. Some studies such as clinical trial in-person focus groups pay as high...
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Mindlance-Cambridge
collection to destruction
Ensure the traceability of associated documentation in the electronic Trial Master File (eTMF)
EDUCATION
Bachelor’s degree required in Biological Sciences, Biomedical Sciences, Biotechnology, Clinical Laboratory Science, Public...
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TekWissen ®-Cambridge
and support to the Translational Science Lead (TSL) to ensure operational implementation and execution of translational science strategies in clinical trials which may include phase I, II and III studies.
• The BTE is responsible for all operational...
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Takeda Pharmaceutical-Cambridge
assessing scientific, medical, and development feasibility, evaluating complete or ongoing clinical trials, assessing regulatory interactions and future development plans.
• For ongoing alliance projects, will interface with partner to achieve Takeda’s...
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Curate Partners-Cambridge
privacy tools, security controls, and data quality frameworks.
Establish architecture standards for sensitive and regulated pharma data, including GxP, HIPAA, GDPR, clinical trial data, patient data, manufacturing quality data, and proprietary R&D data...
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ClinLab Solutions Group-Cambridge
guidelines and regulatory requirements governing clinical trial conduct
• Proven ability to negotiate vendor contracts and manage financial accountability across complex outsourcing arrangements...
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The Lotus Group LLC-Cambridge
We are seeking an experienced Director of Biostatistics to lead statistical strategy and execution for complex, late-stage clinical development programs. In this role, you will design innovative clinical trials, author statistical sections...
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Green Key Resources-Cambridge
development experien
• ceDeep expertise in statistical methodologies for clinical trials, including registration and lifecycle manageme
• ntProven experience interacting with global health authoriti
• esStrong communication skills with the ability to translate...
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Adecco-Cambridge
and laboratory supplies.
• Ensure adherence to Good Laboratory Practice (GLP), Good Clinical Practice (GCP), and applicable quality standards.
Clinical Trial Sample Management Support
• Support biospecimen management activities across clinical studies from...
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adecco.com -
Cambridge
JOB DESCRIPTION
We are seeking an experienced and skilled Clinical Programmer with a strong background within clinical programming. The ideal candidate will have 4-6 years of experience in clinical data programming, with a focus on clinical trial...
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pharmiweb.jobs -
Takeda Pharmaceutical-Cambridge
and negotiation of clinical development plans for potential alliances and or in-licensing opportunities. Assesses scientific, medical, and development feasibility, evaluating strategic fit with overall portfolio, evaluating complete or ongoing clinical trials...
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Takeda Pharmaceutical-Cambridge
of potential business development opportunities and conduct of due diligence evaluations assessing scientific, medical and development feasibility, evaluating complete or ongoing clinical trials, and regulatory interactions and future development plans...
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