Study Start Up - Regulatory Submissions Coordinator London, England

Medpace, Inc.

Full Time London, England 33796 - 36999 GBP ANNUAL Today

Job description

Job Summary :

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. 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.

Entry-level positions are available for recent graduates.

Responsibilities :

Prepare, review, and file clinical trial applications for UK & Ireland;
Provide insightful input on regulatory submissions documents and timelines;
Ensure submissions comply with applicable regulations and guidance documents;
Advise on changing country regulations and compliance requirements; and
Track submissions and ensure timely filing of documents.

Qualifications :

Bachelor's degree (preferably in a Life Sciences field);
Experience in study start-up is essential;
Hands-on experience preparing, reviewing, and submitting regulatory documentation;
Knowledge of Microsoft® Office; and
Excellent organization and communication skills, great attention to detail.

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 4,000 people across almost 40 countries.

Why Medpace? :

When you join Medpace, you become part of a team dedicated to supporting the development of ground-breaking drugs and devices. Our employees provide hope for those living with debilitating diseases. We invite you to be a part of something that is impacting millions of people around the globe while enjoying a competitive total compensation and benefits package and internal growth opportunities.

Organic Growth: Medpace is continuing to grow in all areas globally and has built an expansive research campus at its headquarters in Cincinnati, OH. In 2020, Medpace opened a new seven story building that is approximately 250,000 SQFT. In total, the headquarter's campus includes five buildings and approximately 600,000 SQFT. The company also has expanding office locations in Dallas, TX and Denver, CO.

Perks (vary by location):

On-site gym and swimming pool
Flexible work schedule
Medical and dental insurance
Company pension scheme
Cycle to work scheme
50% reimbursement of commuting expenses & Season Ticket Loan
Annual salary review
Performance-based bonus

Awards:

Medpace historically named a Top Cincinnati Workplace by the Cincinnati Enquirer
Recognized by Forbes as one of America's Best Mid-size Companies in 2021
Medpace ranks amongst top CROs for site ratings across all 10 important attributes including CRA training, preparation & organization, accessibility of staff, open communication, and ensuring timely drug availability
Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility
Ranked in the top 10 on the 2021 LinkedIn Top Companies list in Cincinnati

What to Expect Next:

A member of our recruitment team will review your qualifications and, if interested, you will be contacted for an interview.

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