Good Clinical Practice Jobs in Boston, MA

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Sr. Clinical Trial Associate

Apex Systems

Cambridge, MA, USA

Full-time

Job#: 2006455 Job Description: Senior Clinical Trial Associate, Contract 2006455 Location: Cambridge, MA (Hybrid) Science: Antibody Drug Conjugates Therapeutic Area: Oncology Job Overview: The Sr. CTA will manage the through-put of data inquiries and tracking of clinical data and information. The incumbent will help to fine-tune the tracking, distribution, and storage of critical information that develops during the course of clinical trials. Primary Job Responsibilities:Perform daily and weekl

Clinical Scientist

SGS Consulting

Cambridge, MA, USA

Contract

Job Description: This role is key to help the medical supervision of clinical studies by Clinical Research Directors (CRD) and to ensure scientific management of clinical studies to be performed by the Clinical & Sciences Operations Platform (CSO) and Development Units in client s R&D.The primary purpose of the Clinical Scientist s position is to assist/support the Clinical Research Director in the medical/scientific contribution for the clinical studies e.g: supporting operational activities pe

Senior CGP Auditor

Zachary Piper Solutions, LLC

Boston, MA, USA

Full-time

Piper Health and Sciences is actively seeking a Senior Google Cloud Platform Auditor with proven knowledge of Google Cloud Platform across all phases of Clinical Research. The Senior Google Cloud Platform Auditor will plan and conduct internal and external audits including system audits, supplier audits, safety/pharmacovigilance (PV) audits and others. The Senior Google Cloud Platform Auditor r is a remote, full time opportunity with travel requirements for in-person audit activities. Responsib

Sr. Clinical Trial Manager

Eliassen Group

Cambridge, MA, USA

Contract

Our fast-growing Pharma client is seeking a strong Sr Clinical Trial Manager to join their high performing team to serve as the Unblinded Sr CTM on their program. This Sr CTM will work on a high visibility, large, & fast paced Vaccine Study. This study is outsourced and then has an internal core team comprised of internal employees. Our client is looking for a mature and levelheaded Sr Clinical Trial Manager who can work effectively within a fast-paced environment as an Unblinded part of the

Sr R&D Engineer / Human Factors Engineer

SSI People

Burlington, MA, USA

Contract

Description: Years Experience: 0-6 years of related work experience with a complete understanding of specified functional areas. Skills: Prior engineering skills/experience preferred. Education: Bachelor's degree or an equivalent combination of education and work experience Duties: Responsible for providing engineering support in the creation and the development of new medical device products (invasive and non-invasive). Responsible for compliance with applicable Corporate and Divisional

Sr./Director Clinical Data Management - Oncology

Apex Systems

Cambridge, MA, USA

Full-time

Job#: 2015552 Job Description: Director/Senior Director, Clinical Data Management-Oncology 2015552 Location: Cambridge, MA (Hybrid) Therapeutic Area: Immuno-Oncology Job Overview: We are seeking an experienced Director/Senior Director of Clinical Data Management to oversee all aspects of data management for clinical studies. Primary Job Responsibilities: Serving as the main point of contact for data management activities with clinical and translational CROs, ensuring effective communication and

Medical Device Product Manager

Corps Team Services, LLC

Boston, MA, USA

Full-time

Our client, a medical device company located in Boston, is seeking a Medical Device Product Manager for a direct hire role. This is a hybrid role. The Medical Devices Product Manager will be responsible for leading the development and management of medical device products from concept through to market launch. This role is ideal for candidates with a strong background in biomedical engineering and a blend of skills in quality management, regulatory compliance, and product development. The ideal

Senior Biostatistician

Motion Recruitment Partners, LLC

Andover, MA, USA

Full-time

Our client, a publicly traded medical device company that is a world leader in improving and saving patients lives by transforming the way that organs are transplanted and donated is hiring for a Senior Bioinformatician to join them. Requirements and Qualifications: 6+ years of Experience Programming experience with: SAS, Python or R Masters in Biostatistics, Statistics, Mathematics, or Computer Science Clinical trials experience is a huge plus 2-3x/week in-office Benefits: Health, Dental, Visi

Senior Manager, Biostatistics

AstraZeneca

Boston, MA, USA

Full-time

This is what you will do: The Senior Manager Biostatistics is responsible for statistical activities in support of clinical trials, including but not limited to the following: contributing to trial designs, authoring statistical sections of protocols, preparing statistical analysis plans, and reviewing and interpreting the analysis of clinical trial data. You will be responsible for: Collaborates with Clinical Development, Clinical Pharmacology, Regulatory and Clinical Operations expertise are

Associate Director, Biostatistics

AstraZeneca

Boston, MA, USA

Full-time

This is what you will do: The Associate Director, Biostatistics oversees all biostatistics activities for one or more clinical programs to ensure timely and accurate delivery of statistical designs, analyses, and reports and regulatory submissions. Independently provides strategic statistical input to drug development including feasibility assessments, development plans, complex study designs, cross-study statistical methodology, interpretations, regulatory submissions and follow up. Contributes

Associate Director, Biostatistics

AstraZeneca

Boston, MA, USA

Full-time

This is what you will do: The Associate Director, Biostatistics oversees all biostatistics activities for one or more clinical programs to ensure timely and accurate delivery of statistical designs, analyses, and reports and regulatory submissions. Independently provides strategic statistical input to drug development including feasibility assessments, development plans, complex study designs, cross-study statistical methodology, interpretations, regulatory submissions and follow up. Contributes

Associate Director, Biostatistics

AstraZeneca

Boston, MA, USA

Full-time

This is what you will do: The Associate Director, Biostatistics oversees all biostatistics activities for one or more clinical programs to ensure timely and accurate delivery of statistical designs, analyses, and reports and regulatory submissions. Independently provides strategic statistical input to drug development including feasibility assessments, development plans, complex study designs, cross-study statistical methodology, interpretations, regulatory submissions and follow up. Contributes

Clinical Monitoring Lead

Patel Consultants Corp

Remote

Contract

W-2 Candidates only! Remote position but preferably in Eastern Time Zone. Our client needs a Clinical Monitoring Lead. Responsibilities: Accountable for the execution of monitoring plans & overall quality of monitoring performed by CRAs for assigned US conducted trials (~5-8) across Therapeutic Area(s) phase depending on complexity, size and stage of study.Conduct on-site visits to assess CRA performance, including co-monitoring/supervisory visits, as requested, including oversight of CRAs worki

Scientist, Veterinary Technician

Pfizer

Cambridge, MA, USA

Full-time

Why Patients Need You Pfizer's purpose is to deliver breakthroughs that change patients' lives. Research and Development is at the heart of fulfilling Pfizer's purpose as we work to translate advanced science and technologies into the therapies and vaccines that matter most. Whether you are in the discovery sciences, ensuring drug safety and efficacy or supporting clinical trials, you will apply cutting edge design and process development capabilities to accelerate and bring the best-in-class me

Senior Computational Biologist

Pfizer

Cambridge, MA, USA

Full-time

WHY PATIENTS NEED YOU Pfizer's purpose is to deliver breakthroughs that change patients' lives. Research and Development is at the heart of fulfilling Pfizer's purpose as we work to translate advanced science and technologies into the therapies and vaccines that matter most. Whether you are in the discovery sciences, ensuring drug safety and efficacy or supporting clinical trials, you will apply cutting edge design and process development capabilities to accelerate and bring the best in class me

Associate Director, Biostatistics

AstraZeneca

Boston, MA, USA

Full-time

This is what you will do: The Associate Director, Biostatistics oversees all biostatistics activities for one or more clinical programs to ensure timely and accurate delivery of statistical designs, analyses, and reports and regulatory submissions. Independently provides strategic statistical input to drug development including feasibility assessments, development plans, complex study designs, cross-study statistical methodology, interpretations, regulatory submissions and follow up. Contributes

Associate Director, Scientific Communications Lead

AstraZeneca

Waltham, MA, USA

Full-time

Associate Director, Scientific Communications Lead Waltham, MA or Gaithersburg, MD Are you passionate about communicating scientific findings to drive action and progress? We are seeking a highly motivated and skilled individual to join our team as the Associate Director, Scientific Communications Lead. This role requires independence and dexterity to learn and effectively communicate complex scientific findings at the intersection of Oncology and AI. The individual in this role will additiona

Medical Writer (REMOTE)

NetSource, Inc.

Remote

Contract

PLEASE ONLY SUBMIT YOUR RESUME IF YOU HAVE REGULATORY MEDICAL WRITING EXPERIENCE. ALL OTHER RESUMES WILL BE REJECTED Please note that this is a 6 month contract position. Must have experience writing PLS under EU Clinical Trial Regulation. Must know what the Annex# is. 40 hours /week (Mon Fri) NON NEGOTIABLES: 5 years experience as a regulatory medical writer writing clinical study reports 3 years of Plain Language Summary (PLS) experience 5 years experience writing Clinical study results 3 year

Senior Associate Scientist, Metabolism

Pfizer

Cambridge, MA, USA

Full-time

Why Patients Need You Pfizer's purpose is to deliver breakthroughs that change patients' lives. Research and Development is at the heart of fulfilling Pfizer's purpose as we work to translate advanced science and technologies into the therapies and vaccines that matter most. Whether you are in the discovery sciences, ensuring drug safety and efficacy or supporting clinical trials, you will apply cutting edge design and process development capabilities to accelerate and bring the best in class me

Veeva Vault Architect.

Cognizant Technology Solutions

Boston, MA, USA

Full-time

Veeva Vault Architect. Cognizant Technology Solutions is seeking for "Veeva Vault Architect" who could join in our team of IT professionals in a permanent role. If you meet our background requirements and skills and looking for an opportunity to be rewarded for your skills and expertise, here is the ideal opportunity for you! About Us: Cognizant (Nasdaq: CTSH) is one of the world's leading professional services companies, redefining clients' business, operating, and technology models for the d