Study Start-Up Project Manager
Irving, TXFull-time
Behavioral Health Market Context
Apply Nowvia Medpace Careers
Benefits
Paid Time OffHealth Insurance
Job Description
management process at Medpace.
Incentives can include: Competitive bonus program, sign-on/relocation bonus, and equity awards.
Location: Position is based in Dallas, TX.
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
• Experience with Cardiovascular and Metabolic indications in an academic and/or clinical trial setting is desired, such as, but not limited to, NASH, diabetes, medical devices and coronary artery diseases.
• 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 Overview
Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.
Why Medpace?
People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.
The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.
Dallas Perks
• Dallas Campus Overview
• Flexible work environment
• Competitive PTO packages, starting at 20+ days
• Competitive compensation and benefits package
• Company-sponsored employee appreciation events
• Employee health and wellness initiatives
• Community involvement with nonprofit organizations
• Structured career paths with opportunities for professional growth
• Discounts on local sports games, fitness gyms and attractions
• Modern, ecofriendly campus with an on-site fitness center
• Free on-site parking
• Outdoor seating and workspace
Awards
• Named a Top Workplace in 2024 by The Cincinnati Enquirer
• Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
• Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility
What to Expect Next
A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.
Incentives can include: Competitive bonus program, sign-on/relocation bonus, and equity awards.
Location: Position is based in Dallas, TX.
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
• Experience with Cardiovascular and Metabolic indications in an academic and/or clinical trial setting is desired, such as, but not limited to, NASH, diabetes, medical devices and coronary artery diseases.
• 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 Overview
Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.
Why Medpace?
People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.
The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.
Dallas Perks
• Dallas Campus Overview
• Flexible work environment
• Competitive PTO packages, starting at 20+ days
• Competitive compensation and benefits package
• Company-sponsored employee appreciation events
• Employee health and wellness initiatives
• Community involvement with nonprofit organizations
• Structured career paths with opportunities for professional growth
• Discounts on local sports games, fitness gyms and attractions
• Modern, ecofriendly campus with an on-site fitness center
• Free on-site parking
• Outdoor seating and workspace
Awards
• Named a Top Workplace in 2024 by The Cincinnati Enquirer
• Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
• Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility
What to Expect Next
A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.
Qualifications
- •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
- •Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility
Benefits
- •Incentives can include: Competitive bonus program, sign-on/relocation bonus, and equity awards
- •Dallas Campus Overview
- •Flexible work environment
- •Competitive PTO packages, starting at 20+ days
- •Competitive compensation and benefits package
- •Company-sponsored employee appreciation events
- •Employee health and wellness initiatives
- •Community involvement with nonprofit organizations
- •Structured career paths with opportunities for professional growth
- •Discounts on local sports games, fitness gyms and attractions
- •Modern, ecofriendly campus with an on-site fitness center
- •Free on-site parking
- •Outdoor seating and workspace
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
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