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    • Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical,…
    • View all Medpace, Inc. jobs - Stirling jobs - Study Manager jobs in Stirling
    • Salary Search: Regulatory Submissions (Study Start-up) Manager salaries
    • See popular questions & answers about Medpace, Inc.
    • Strong industry experience in medical devices or a diagnostics background.
    • Participating in all sales and marketing meetings.
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    • Guide clients on integrated marketing/communications decisions, identifying new opportunities to increase visibility their brand including consultative selling.
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    • *Field-based role covering Scotland*.
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    • The Territory Manager purpose in this role is to effectively increase sales volume and revenue through medical device product sales year on year, whilst…
    • Relevant degree in a science subject or communications/marketing.
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    • Gilead’s therapeutic areas of focus include liver diseases, infectious diseases, inflammatory diseases, haematology and oncology.

Job Post Details

Regulatory Submissions (Study Start-up) Manager - job post

Medpace, Inc.
2.6 out of 5 stars
Wallace House 17-21 Maxwell Place, Stirling FK8 1JU
Full-time
You must create an Indeed account before continuing to the company website to apply

Job details

Job type

  • Full-time

Location

Wallace House 17-21 Maxwell Place, Stirling FK8 1JU

Benefits

Pulled from the full job description

  • Annual leave
  • Work from home
  • Company events

Full job description

Job Summary :
Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, office-based, Regulatory Submissions Manager to join our Clinical Operations team. This position plays a key role in the clinical trial management process at Medpace. 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.
Responsibilities :
  • Efficiently manage and successfully execute all aspects of global start-up;
  • Perform quality checks on submission documents and site essential documents;
  • Prepare and approve informed consent forms;
  • Review pertinent regulations to develop proactive solutions to start-up issues and challenges; and
  • Present during bid defenses, general capabilities meetings, and audits.
Qualifications :
  • Extensive experience in clinical research, preferably with a CRO. Experience may include CRA or project management experience;
  • Knowledge and experience of Clinical Trial Applications within Europe;
  • Strong oral and written communication skills; and
  • Team oriented approach and strong leadership skills.
Medpace Overview :
Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV 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 the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.
Why Medpace? :
When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.

Purpose-Driven Work
    • Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence

Collaborative Culture
    • Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.
    • Leadership throughout Medpace is both accessible and approachable

Continuous Growth & Development
    • Office based environment with on-site mentors
    • Defined career paths with clear advancement opportunities
    • Industry renowned onboarding and training programs designed to accelerate professional development
    • Ongoing training and continuous learning opportunities throughout your career
    • An environment that encourages employees to influence change, contribute ideas, and grow quickly

Other Employee Benefits
    • Competitive compensation programs that recognize and reward performance
    • Comprehensive health, wellness, retirement, and PTO benefits
    • Office based culture with occasional WFH that provides flexibility for eligible positions after training
    • Company-sponsored social events

Please note benefits may vary based on country.

What to Expect Next
A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.
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