Senior Clinical Research Associate - FSP
United Kingdom, Remote Job ID R0000028325 Category Clinical Trials Date Posted 11/15/2024Overview
As a Clinical Research Associate (CRA) at Parexel, you act as an integral part to get treatments to patients sooner. Our CRAs' priority is the safety and well-being of the patients. As you travel to investigator sites and perform your monitoring duties, we encourage you to be inquisitive, take accountability, build relationships, and act with integrity.
Join a team with a wide variety of experiences and knowledge, and work on global projects within a broad scope of therapeutic areas. We’re looking for people who want to grow personally and professionally and support their colleagues globally and cross-functionally.
Success Profile
Do you have these soft skills and interpersonal traits to succeed at Parexel?
- Communicator
- Detail-oriented
- Flexible
- Organized
- Problem-solver
- Self-starter
About This Role
Parexel is currently seeking a Senior Clinical Research Associate to support us in the UK, assigned to one of our key sponsors.
Working as a Senior Clinical Research Associate at Parexel FSP offers tremendous long-term job security and prospects.
We undertake vital clinical studies for sponsors including the leading global biotechs and Pharma top 50. And we have an incredible pipeline of work.
Whether you see your future path as a CRA, or in fields such as clinical operations, project management, line management, or other positions, we have a world of opportunity waiting for you.
Our CRAs work from their home office base, supporting studies within their country or region. ‘Manageable sites, manageable protocols’ is our mantra. Expect exciting professional challenges in inspiring studies, but with time for your outside life.
Some specifics about this advertised role
Dedicated to one client.
Responsible for all site management and monitoring activities across assigned oncology studies
Work with industry leaders and subject matter experts.
Opportunity to mentor junior CRAs.
Work with world-class technology.
a pivotal role in the drug development process.
Here are a few requirements specific to this advertised role.
Substantial Site Management experience, with an understanding of the clinical trial methodology and terminology.
Experience in, or willingness to monitor oncology clinical trials.
Experience in independent monitoring, all types of visits.
Effective time management, organizational and interpersonal skills & problem-solving skills, with the ability to multi-task and prioritize.
Good understanding and working knowledge of clinical research, phases of clinical trials, current GCP/ICH & country clinical research law & guidelines.
#LI-REMOTE
Potential Career Path
Parexel offers various career paths and internal development programs for CRAs to advance to the next level. This could include enhancing your technical position, moving into management, or shifting to other areas of the business.
- APEX CRA
- CRA I
- CRA II
- Senior CRA
- Project ManagementSubject Matter ExpertPeople Management
Employee Insights
TEAM IMPRESSIONS
Why Clinical Research Associates work at Parexel
