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Research Study Jobs in Cambridge

1 - 15 of 38
Search jobs in
1 - 15 of 38
Search Results - Research Study Jobs in Cambridge
Abacus Service Corporation-Cambridge
Description: Research Associate II - In-vivo Onsite role in Cambridge, MA The purpose of this position is to conduct in-vivo toxicology experiments using a broad range of scientific and technical skills to deliver high-quality data...
resume-library.com -
Microsoft-Cambridge
Microsoft Research (MSR) AI Frontiers is inviting applications for a Principal Researcher to join our team. We are focused on solving real-world problems and pushing the boundaries of agentic AI systems and interaction research. The mission...
US Tech Solutions-Cambridge
Duration: 12 Months Contract Employment Type: W-2 Job Description: The Associate Director of US Health Economics and Outcomes Research & Real-World Evidence (HEOR & RWE) contractor will help develop real-world and economic evidence generation...
mindmatch.ai -
Pfizer-Cambridge
The purpose of Director of Clinical Research role is to coordinate and lead the development of first in man (FIH), proof of mechanism (POM), proof of clinical activity (SoCA) and proof of concept (PoC) and dose ranging studies for novel biological...
dejobs.org -
AbbVie-Cambridge
into research or development programs. Responsibilities: Contribute to clinical development by supporting Phase 1-4 studies including study design, and clinical pharmacology strategy. Author regulatory documents including protocols, study reports, population...
resume-library.com -
Cedent Consulting-Cambridge
Summary: This role is ideal for someone with a strong background in clinical research and drug development. The position involves shaping and driving the clinical development process, contributing to clinical program strategy and execution...
Takeda-Cambridge
The Director Clinical Science - M.D. is responsible for providing strategic direction and oversight in clinical research, ensuring the successful execution of major initiatives. This role focuses on designing clinical studies, managing safety...
mindmatch.ai -
Katalyst Healthcares & Life Sciences-Cambridge
to incorporate production code macros in studies required, ability to execute programming assignment and problem solve issues independently, and ability to present complex research and data clearly to stakeholders. Experience and/or training in the application...
resume-library.com -
Sarepta Therapeutics-Cambridge
activities within Sarepta that positively impacts our clinical programs. The Director of Feasibility & Study Start-up will report to the Sr. Director, Clinical Operations, Feasibility & Study Start-up, Early Research and RWE and lead a team to drive...
surfingwave.app -
Delphia Therapeutics-Cambridge
efficacy studies in collaboration with a contract research organization in order to support program goals and objectives.  •  Prepare regulatory submission documentation, author in vivo pharmacology sections of regulatory documents.  •  Identify and manage...
mindmatch.ai -
Katalyst Healthcares & Life Sciences-Cambridge
Responsibilities: Leads all DM lifecycle activities, from study start-up, maintenance, database lock and close-out. Independently develop DM documents including but not limited to Data Management Plans (DMP), Case Report Forms (CRFs), CRF...
resume-library.com -
Takeda Pharmaceutical-Cambridge
of reaction & particle engineering, including the development of scale down models for the study of unit operations, process safety evaluation as well as technical transfer to external contract manufacturing organizations. He or she will be collaborating...
AbbVie-Cambridge
PK/PD study proposals and leads those efforts. Anticipates and critically evaluates Clinical Pharmacology, PK/PD or regulatory advances, strengths, weaknesses, opportunities and threats, and responds with appropriate new strategies. Consistently...
resume-library.com -
Pfizer-Cambridge
advanced methods for innovative research in drug discovery. + Collaborate with team members in performing data analyses and integrating resources to provide novel insights into disease biology and therapeutics. + Communicate analyses and study...
dejobs.org -
Cambridge
and general knowledge of industry practices and standards.  •  Familiarity with CDISC (Clinical Data Interchange Standards Consortium) standards, such as SDTM (Study Data Tabulation Model), ADaM (Analysis Data Model), and CDASH (Clinical Data Acquisition...
pharmiweb.jobs -
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