Sr. Clinical Project Manager

Proclinical Group; Boston (MA); Remote; USD 125,000 - 150,000; Full time

Job summary

A leading life sciences recruiter is seeking a Senior Clinical Project Manager to lead global clinical trials in oncology. This remote role involves managing project teams, ensuring compliance with regulations, and overseeing study execution. Ideal candidates will possess a Bachelor's degree in health sciences and have substantial experience in clinical research.

Qualifications

• Bachelor's degree in health sciences or related field required.
• Experience in clinical research and study management is essential.
• Knowledge of FDA Regulations and ICH-GCP guidelines preferred.

Responsibilities

• Oversee study execution and manage CROs, vendors, and consultants.
• Lead risk management efforts and ensure compliance with regulations.
• Drive clinical program timelines and provide mentoring to junior team members.

Skills

Clinical research

Study management

Communication

Collaboration

Oncology knowledge

Education

Bachelor's degree in health sciences or related field

Tools

Excel

Word

PowerPoint

Outlook

MS Project

Job description

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 [e-mail]

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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