Clinical Trial Associate - FSP - Remote
United Kingdom, Remote Additional Locations Romania-Remote; Serbia-Remote; Spain-Remote Job ID R0000034077 Category Project Leadership Date Posted 06/17/2025Overview
As a part of the global Project Leadership group at Parexel, you are responsible for leading cross-functional teams to deliver high-quality and patient-focused clinical trials and help bring life-changing treatments to market faster. You collaborate with clients and internal stakeholders to identify project requirements, develop project plans, and manage project timelines and budgets. The role requires strong leadership and communication skills, the ability to work under pressure, and a passion for improving patients' lives.
In return, Parexel offers a supportive work environment, and a high degree of empowerment and accountability to lead your studies. Within this role, you work with a diverse set of clients and therapeutic areas, and you are encouraged to take on new challenges and pursue your interests.
Success Profile
Do you have these soft skills and interpersonal traits to succeed at Parexel?
- Adaptable
- Communicator
- Collaborative
- Leadership
- Proactive
- Problem-solver
About This Role
Parexel are currently recruiting for an experienced Clinical Trial Associate/Administrator to support a large global cardiology study.
In this position you will be an invaluable resource, providing support to the wider clinical study teams, helping to maintain system accuracy and ensuring on time delivery of clinical trial deliverables
Some specifics about this advertised role
- Assist with the in-house coordination of activities related to the conduct of clinical trials
- Track progress across multiple programs and communicate this to internal and external stakeholders
- Assist in maintaining clinical invoice tracking and other budget databases for multiple projects; generate periodic reports on status of payments and other database reports, and resolve payment inquiries from investigator sites
- Maintain informational databases for clinical trial status throughout the life of a clinical program
- Responsible for the assembly, review, quality control, and tracking of regulatory documents
- Perform maintenance and tracking of study materials including investigational drug
- Organize trial and program related team meetings, associated agendas, and generate meeting minutes, including tracking of action items
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.
What we are looking for in this role
For every role, we look for professionals who have the determination and courage always to put patient well-being first.
That to us is working with heart.
Here are a few requirements specific to this advertised role.
- BS/ BA degree is preferred.
- Minimum 1+ years of clinical research experience gained with a CRO, Biotech or Pharmaceutical Company working on Phase 1-4 clinical trials.
- Experience supporting global/regional trials is essential
#LI-REMOTE
Potential Career Path
Parexel offers a growth path with diverse therapeutic areas and clients, so you can grow according to your interests.
- Associate Project Leader
- Project Leader
- Senior Project Leader
- Associate Project Director
- Project Director
- Director, Project Leadership
- Senior Director, Project Leadership
Employee Insights
Why Project Leaders work at Parexel
