At a Glance
- Tasks: Support regulatory submissions and ensure compliance with regulations.
- Company: Dynamic life sciences company focused on innovation and collaboration.
- Benefits: Flexible work environment, competitive pay, and great PTO packages.
- Other info: Structured career paths and employee appreciation events for a supportive workplace.
- Why this job: Join a team making a real difference in clinical trials and patient care.
- Qualifications: Bachelor's in Life Sciences and 2 years as a Regulatory Submissions Coordinator.
The predicted salary is between 35000 - 45000 £ per year.
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.
Additional Responsibilities
- Prepare, review, and file clinical trial applications;
- Communicate with research sites to collect all essential documents required before the site starts to enroll patients;
- Provide insightful input on regulatory submission 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
Join our dynamic Clinical Operations team in London, where we prioritise employee growth and foster a collaborative work culture. As a Clinical Trial Site Relationship Coordinator, you'll benefit from ongoing professional development opportunities while working in a vibrant environment that values strategic relationships and innovative solutions in clinical research. Enjoy the unique advantage of reduced travel while making a meaningful impact in the field of clinical trials.
We think you need these skills to ace Experienced Regulatory Submissions Coordinator in Stirling
Communication Skills
Problem-Solving Skills
Organizational Skills
Adaptability
Flexibility
Compassion
Teamwork
