Medpace
Contract Manager (Dallas)
Medpace, Dallas, Texas, United States, 75215
Job SummaryWe are growing rapidly, and currently seeking a full-time office-based Site Contract Manager to join our Clinical Operations team. This position will work on a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you! Incentives are available.
Responsibilities
End-to-end management of the clinical trial agreement (CTA) process for global, multi-site clinical trials
Develop the study-specific CTA strategy with the Sponsor and internal stakeholders
Develop country-specific CTA templates
Negotiate CTAs and the corresponding budget directly with sites
Present progress to internal and external stakeholders ensuring deliverables are met within agreed upon timelines.
Qualifications
Bachelor’s degree in relevant legal or business field;
A minimum of 4 years’ industry experience with considerable contract and budget negotiation experience
Ability to effectively influence others
Exceptionally strong communication skills
Advanced knowledge of Microsoft Word, Excel, and PowerPoint
Travel:
minimal
Medpace OverviewMedpace 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 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
Hybrid work-from-home options (dependent upon position and level)
Competitive PTO packages, starting at 20+ days
Flexible work hours
Company-sponsored employee appreciation events
Employee health and wellness initiatives
Flexible work schedule
Competitive compensation and benefits package
Structured career paths with opportunities for professional growth
Annual bonus and merit programs*
Discounts on local sports games, local fitness gyms and attractions
Free on-site parking
10 Balconies with Outdoor seating
47,338 SF completely remodeled office in 2020
Awards:
Recognized by Forbes as one of America's Best Mid-size Companies in 2021 and 2022
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.
EO/AA Employer M/F/Disability/Vets
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Responsibilities
End-to-end management of the clinical trial agreement (CTA) process for global, multi-site clinical trials
Develop the study-specific CTA strategy with the Sponsor and internal stakeholders
Develop country-specific CTA templates
Negotiate CTAs and the corresponding budget directly with sites
Present progress to internal and external stakeholders ensuring deliverables are met within agreed upon timelines.
Qualifications
Bachelor’s degree in relevant legal or business field;
A minimum of 4 years’ industry experience with considerable contract and budget negotiation experience
Ability to effectively influence others
Exceptionally strong communication skills
Advanced knowledge of Microsoft Word, Excel, and PowerPoint
Travel:
minimal
Medpace OverviewMedpace 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 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
Hybrid work-from-home options (dependent upon position and level)
Competitive PTO packages, starting at 20+ days
Flexible work hours
Company-sponsored employee appreciation events
Employee health and wellness initiatives
Flexible work schedule
Competitive compensation and benefits package
Structured career paths with opportunities for professional growth
Annual bonus and merit programs*
Discounts on local sports games, local fitness gyms and attractions
Free on-site parking
10 Balconies with Outdoor seating
47,338 SF completely remodeled office in 2020
Awards:
Recognized by Forbes as one of America's Best Mid-size Companies in 2021 and 2022
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.
EO/AA Employer M/F/Disability/Vets
#J-18808-Ljbffr