Clinical Research Associate I & II (FSP) - Ankara or Istanbul

Parexel FSP is currently seeking Clinical Research Associate I

and CRAII. Home-based in Istanbul or Ankara.

Open to Clinical Research Associates with a minimum of 1 year

of experience onsite monitoring in Turkey for CRAI and 2 years experience

for CRAII.​

Working as a 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.

Great opportunities to travel, work from home, meet new people, and play

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.