(Sr.) Clinical Trial Manager

Boston Full-Time 72000 - 84000 £ / year (est.) No home office possible

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This range is provided by Genepool Networks. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$90.00/hr – $100.00/hr

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Executive Search | Recruitment Professional

Overview:

Genepool Networks is excited to connect with experienced Clinical Trial Managers (CTMs) and Senior Clinical Trial Managers (Sr. CTMs) to oversee the planning, execution, and completion of clinical studies. If you’re passionate about collaborating closely with internal teams, external vendors, and clinical sites to ensure trials are conducted efficiently, within budget, and in compliance with regulatory standards, read on!

Key Responsibilities:

Study Oversight: Lead the operational aspects of clinical trials from initiation to close-out, ensuring adherence to protocols, timelines, and budgets.

Vendor Management: Coordinate with Contract Research Organizations (CROs), laboratories, and other third-party vendors to align with study objectives and deliverables.

Site Coordination: Manage site selection, initiation, monitoring, and close-out activities, maintaining strong relationships with investigators and site staff.

Regulatory Compliance: Ensure all trial activities comply with Good Clinical Practice (GCP), International Council for Harmonization (ICH) guidelines, and applicable regulatory requirements.

Data Integrity: Collaborate with data management teams to oversee data collection, query resolution, and database lock processes.

Risk Management: Identify potential risks to study timelines or data quality and implement mitigation strategies promptly.

Documentation: Maintain accurate and up-to-date trial documentation, including Trial Master Files (TMFs), monitoring reports, and study logs.

Cross-functional collaboration: Work closely with clinical operations, regulatory affairs, medical writing, and other departments to ensure cohesive study execution.

Training: Provide training and guidance to site personnel and internal team members on study protocols and procedures.

Qualifications:

Bachelor’s degree in Life Sciences, Nursing, or a related field; advanced degree preferred.

Minimum of 3–5 years of experience in clinical trial management, preferably within a sponsor organization.

Demonstrated experience in oncology clinical trials is highly desirable.

Comprehensive knowledge of clinical research processes, GCP, ICH guidelines, and FDA regulations.

Proven ability to manage multiple studies or projects simultaneously.

Excellent organizational, communication, and interpersonal skills.

Proficiency in Microsoft Office Suite and clinical trial management systems (CTMS).

Preferred Experience:

Experience with early-phase (Phase I/II) and late-phase (Phase III) clinical trials.

Familiarity with electronic data capture (EDC) systems and other clinical trial technologies.

Ability to travel as required to oversee site activities and attend meetings.

We value building relationships with talented professionals prioritizing exceptional alignment in their plans for career progression. If you\’re interested in overseeing impactful clinical studies and collaborating with dynamic internal teams, external vendors, and clinical sites, we’d love to hear from you.

Seniority level

Seniority level

Mid-Senior level

Employment type

Employment type

Contract

Job function

Job function

Project Management
Industries

Biotechnology Research and Pharmaceutical Manufacturing

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