Clinical Trial Coordinator - UK - London, Hybrid - FSP - REGISTER YOUR INTEREST

When our values align, there's no limit to what we can achieve.
 
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

REGISTER YOUR INTEREST for upcoming Clinical Trial Coordinator roles with Parexel FSP in the UK.

Office based in London, with the flexibility to go to the office as a minimum of two days per week and based on the business need.

Open to candidates with experience as Clinical Trial Assistant, Study Coordinator, Clinical Trial Coordinator, Project Support Associate, Project Specialist, ICRA, or similar.

Play a pivotal role in some of the most significant clinical studies taking place today!

Single sponsor dedicated to a legendary pharmaceutical R&D powerhouse. A top 10 company and the name behind an incredible array of medicines, therapies, and vaccines. Collaborate, and learn, alongside some of the industry’s most experienced people.

Working as a Clinical Trials Coordinator at Parexel FSP provides an exciting platform for your skills, as well as the potential to develop into a variety of career paths. We make a difference in millions of lives. We’ll do the same for your career!

Primary Responsibilities:

The Clinical Trial Coordinator (CTC) will support the Clinical Research Manager (CRM) and other team members through the life cycle of the study from study start-up to study closure

Support the team members through the life cycle of a clinical trial from study start-up to study closure, performing the following duties:

• Trial and site administration and support.

• Collaborate with finance/budgeting representatives.

• Meeting Planning.

• Interact with internal and external stakeholders (study sites, vendors, etc.) in support of clinical study objectives.

• Tracking and reporting negotiations.

• Ensuring compliance with financial procedures.

• Maintenance of tracking tools and systems.

• Collate, distribute, and archive clinical documents.

• Assist with electronic Trial Master File reconciliation.

• Budgeting, Agreement, and Payments: Collaborate with finance/budgeting representatives.

• Meeting Planning.

Education and Experience:

• B.A./B.S. (Life Sciences preferred) or equivalent healthcare experience.

• Minimum 1-2 years in Clinical Research in a similar role.

• Fluent in Local Languages and business proficient in English (verbal and written).

• Good understanding of Global, Country/Regional Clinical Research guidelines.

• Effective time management, organizational and interpersonal skills, conflict management.

• Effective communication with external customers (e.g., sites and investigators).

• Able to work independently.

We care about our people and your passion, as they are the key to our success, and provide an open and friendly work environment where we empower people and provide them with opportunities to develop their long-term careers. In addition, you will have the opportunity to develop within your role and tackle further responsibilities or develop your skill set within other related departments of Parexel.

Who are Parexel

Parexel supports clinical studies across the full range of therapeutic areas, and we have longstanding partnerships with a vast client base.

We supported the trials of most of today’s top 50 best-selling drugs, but equally we enable more niche drug developments that are critical to the well-being of many patients.

You’ll be an influential member of the wider team.

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