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Clinical Research Associate

extra holidays - extra parental leave - fully flexible

Remote:

Full Remote

Contract:

Full time

Experience:

Senior (5-10 years)

Work from:

Turkey

Offer summary

Qualifications:

Substantial site management experience, Understanding of clinical trial methodology, Experience in oncology clinical trials, Good knowledge of GCP/ICH guidelines, Effective time management and organizational skills.

Key responsabilities:

Manage site activities for oncology studies
Mentor junior CRAs
Collaborate with industry leaders
Conduct independent monitoring visits
Utilize world-class technology in studies

Parexel Pharmaceuticals XLarge http://www.parexel.com/

10001 Employees

See more Parexel offers

Job description

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.

Parexel is currently seeking a Senior Clinical Research Associate to support us in Turkey, 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.

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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