Experienced Study Start-Up Project Manager (Remote)

Medpace, Inc.; United States; Remote; USD 90,000 - 120,000; Full time

Benefits offered by this job

Flexible work environment

Competitive PTO packages – starting at 20+ days

Employee health and wellness initiatives

Competitive compensation and benefits package

Structured career paths with opportunities for professional growth

Job summary

Medpace is seeking a full-time Global Study Start-Up Project Manager to join their Clinical Operations team. The role requires leading the execution of global studies, ensuring regulatory compliance, and managing quality checks. Candidates must hold a Bachelor's degree and have over 5 years of clinical research experience, ideally in a senior role at a CRO. This position allows for remote work, competitive pay, and includes various perks such as generous PTO, career growth opportunities, and employee wellness initiatives.

Qualifications

• 5+ years of experience in clinical research, preferably in a Senior/Lead role at a CRO in Study Start-Up.
• Demonstrated role in developing others.
• Strong communication skills required.

Responsibilities

• Manage successful execution of global start-up, maintenance, and close-out studies.
• Lead others in a matrix environment.
• Perform quality checks on submission documents.

Skills

Project management

Oral and written communication

Leadership in a matrix environment

Education

Bachelor's degree

Advanced degree in Life Sciences

Job description

Job Summary

Do you enjoy working in a fast-paced environment where you are empowered to make strategic decisions and contribute to a growing and profitable company? Join us at Medpace! Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, Global Study Start-Up Project Manager to join our Clinical Operations team. This position plays a key role in the clinical trial management process at Medpace.

Incentives can include: Competitive bonus program, sign-on bonus, and equity awards.

Location: Remote

Responsibilities

• Efficiently manage successful execution of global start-up, maintenance, and close-out studies;
• Effectively lead others in a matrix environment;
• Perform quality checks on submission documents and site essential documents;
• Prepare and approve informed consent forms;
• Serve as a Sponsor point of contact for start-up and regulatory submissions items;
• Review pertinent regulations to develop proactive solutions to start-up challenges;
• Prepare new business proposals and present during bid defenses, general capabilities meetings, and audits;
• Contribute to the growth and development of departmental staff, processes and systems.

Qualifications

• Bachelor's degree required, advanced degree in Life Sciences preferred
• 5+ years of experience in clinical research, preferably in a Senior/Lead role at a CRO in Study Start-Up
• Project management experience and demonstrated role in developing others
• Strong oral and written communication skills required

Travel: Minimal

Medpace Perks

• Flexible work environment
• Competitive PTO packages – starting at 20+ days
• Company-sponsored employee appreciation events
• Employee health and wellness initiatives
• Competitive compensation and benefits package
• Structured career paths with opportunities for professional growth
• Discounts for local businesses