At a Glance
- Tasks: Support regulatory submissions and manage clinical trial documentation.
- Company: Join a rapidly growing clinical operations team at Medpace.
- Benefits: Enjoy flexible work, competitive pay, and great career growth opportunities.
- Other info: Be part of a supportive environment with employee appreciation events.
- Why this job: Make a real impact in clinical trials and enhance your professional skills.
- Qualifications: Bachelor's in Life Sciences and 2 years of regulatory submissions experience required.
The predicted salary is between 30000 - 40000 £ per year.
Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, office-based Regulatory Submissions Coordinator to join our Clinical Operations team. This position plays a key role in the clinical trial management process at Medpace.
Responsibilities
- Provide day-to-day departmental support activities to Regulatory Submissions Coordinators;
- Maintain database and spreadsheets as necessary to facilitate tracking and documentation of departmental activities;
- Collect, review, organize, and assemble regulatory start-up submissions;
- Perform other tasks as needed;
- Prepare, review, and file clinical trial applications;
- Communicate with research sites (hospitals, etc.) to collect all essential documents required before the site starts to enrol patients to participate in the clinical trial;
- Provide insightful input on regulatory submissions documents and maintain timelines for study start-up through both internal and external collaboration;
- Ensure submissions comply with applicable regulations and guidance documents.
Qualifications
- Bachelor's degree in a Life Sciences field;
- At least 2 years of work experience as a Regulatory Submissions Coordinator;
- Hands-on experience preparing, reviewing, and submitting regulatory documentation;
- Knowledge of Microsoft Office;
- Excellent organization and communication skills;
- Great attention to detail.
Benefits
- Flexible work environment;
- Competitive compensation and benefits package;
- Competitive PTO packages;
- Structured career paths with opportunities for professional growth;
- Company-sponsored employee appreciation events;
- Employee health and wellness initiatives.
Experienced Regulatory Submissions Coordinator in Stirling employer: Medpace, Inc.
Medpace, Inc. is an excellent employer for those seeking a dynamic role as a Feasibility Data Visualization Analyst in London. With a flexible work environment, competitive compensation, and a strong focus on structured career development, employees are empowered to grow and thrive while collaborating closely with clinical operations and medical teams to enhance data strategies. This supportive culture fosters innovation and meaningful contributions to clinical research.
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We think this is how you could land Experienced Regulatory Submissions Coordinator in Stirling
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We think you need these skills to ace Experienced Regulatory Submissions Coordinator in Stirling
Some tips for your application 🫡
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Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at Medpace, Inc. that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
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If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.
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