Sr. Clinical Project Manager

Proclinical Staffing

Boston (MA)

Remote

USD 96,432 - 123,984

Full time

14 days+

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Job summary

Proclinical Staffing is seeking a Senior Clinical Project Manager to lead global clinical trials in oncology. This remote position requires expertise in managing project teams, ensuring compliance with regulations, and overseeing study execution. The ideal candidate will have a Bachelor's degree in health sciences and experience in clinical research.

Qualifications

Experience in clinical research and study management.
Proficient in managing CROs, vendors, and consultants.
Ability to travel as needed.

Responsibilities

Oversee study execution, including management of CROs, vendors, and consultants.
Manage individual study projects, ensuring milestones are met.
Ensure compliance with ICH-GCP, federal, and local regulations.

Skills

Communication

Collaboration

Knowledge of FDA Regulations

Therapeutic knowledge in oncology

Education

Bachelor's degree in health sciences or related field

Tools

Excel

Word

PowerPoint

Outlook

MS Project

Job description

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

Base pay range

$70.00/hr - $90.00/hr

Direct message the job poster from Proclinical Staffing

Recruiting Life Sciences Professionals across the North America

Sr. Clinical Project Manager - Contract - Boston - REMOTE

Are you a dedicated individual looking to put your expertise to work fully flexibly in a remote position?

Proclinical is seeking a Senior Clinical Project Manager to lead the planning and execution of large, global clinical trials in oncology.

Primary Responsibilities:

The successful candidate will be involved in managing project teams to ensure timelines and budgets are met, with a focus on operational leadership within clinical development.

Skills & Requirements:

Bachelor's degree in health sciences or related field.
Experience in clinical research and study management.
Proficient in managing CROs, vendors, and consultants.
Knowledge of FDA Regulations and ICH-GCP guidelines.
Strong communication and collaboration skills.
Therapeutic knowledge in oncology preferred.
Proficient in Excel, Word, PowerPoint, Outlook, and MS Project.
Ability to travel as needed.

The Sr. Clinical Project Manager's responsibilities will be:

Oversee study execution, including management of CROs, vendors, and consultants.
Manage individual study projects, ensuring milestones are met and metrics tracked.
Lead risk management efforts and report progress to senior leadership.
Guide investigator recruitment and ensure staff training on guidelines and SOPs.
Ensure compliance with ICH-GCP, federal, and local regulations.
Contribute to clinical documentation and regulatory submissions.
Maintain responsibility for study-related operational plans and quality management.
Participate in forecasting and managing clinical trial supplies.
Ensure proper maintenance of the Trial Master File.
Respond to Quality Assurance audits and regulatory inspections.
Facilitate development of clinical trial agreements and manage budgets.
Drive clinical program timelines and goals, and provide mentoring to junior team members.

Compensation:

$70.00 - $90.00 Per Hour

If you are having difficulty in applying or if you have any questions, please contact Bodin Forsen at b.forsen@proclinical.com

If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.

Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.

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Seniority level