PRA Health Sciences

Clinical Research Associate - Phase I

Location
Hungary, Home based, Budapest
Salary
Competitive
Posted
13 Feb 2021
Closes
15 Mar 2021
Ref
HH2020-71443
Discipline
Clinical Research
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)

One thing we all have in common is the drive to produce great results for our clients and to advance treatment options available to patients worldwide. We always have a desire to keep seeking new and better ways to operate, to achieve these results. Enter: the Strategic Solutions Division.

As an Early Phase Clinical Research Associate, you will be dedicated to one of our global pharmaceutical clients; a client with which PRA shares a culture of innovation, flexibility and a common vision of bringing life-improving drugs to market. Leading by example, you can set the standard of excellence and enjoy a challenging career in this exclusive program.

The Clinical Research Associate is ultimately responsible for the successful management of investigator sites and monitoring activities for assigned clinical studies throughout the trial life-cycle.

Key responsibilities include:

- Full ownership of investigator sites for assigned studies, with responsibility for the successful management of the site right through to close-out, in accordance with the clinical monitoring plan.

- Developing effective relationships with investigator site staff to ensure that key clinical metrics are met.

- Ensuring integrity of clinical data through an ability to sufficiently maintain site tracking records and working diligently to relevant guidelines.

You are:

Passionate, innovative and committed.

Here at PRA we want our employees to succeed and ensure that they are set up for this success through constant training, development and support. To enable success in this position you will have:

- Prior experience of working in investigator site management, including conducting monitoring visits, from either a pharmaceutical company or a CRO environment.

-Experience in supporting Phase I studies

- A working knowledge of ICH-GCP guidelines and local and international regulatory requirements is essential.

- You will be educated to degree level in a life science discipline or be a licensed healthcare professional.

- Fluent Hungarian and English language is a must.

Your health, your family, your career, your money — the things that matter to you, matter to us. The benefits of PRA just get better and better.

PRA Health Sciences is an Equal Opportunity Employer. We welcome and encourage diversity in the workplace.

You are:

Passionate, innovative and committed.

Here at PRA we want our employees to succeed and ensure that they are set up for this success through constant training, development and support. To enable success in this position you will have:

- Prior experience of working in investigator site management, including conducting monitoring visits, from either a pharmaceutical company or a CRO environment.

-Experience in supporting Phase I studies

- A working knowledge of ICH-GCP guidelines and local and international regulatory requirements is essential.

- You will be educated to degree level in a life science discipline or be a licensed healthcare professional.

- Fluent Hungarian and English language is a must.

Your health, your family, your career, your money — the things that matter to you, matter to us. The benefits of PRA just get better and better.

PRA Health Sciences is an Equal Opportunity Employer. We welcome and encourage diversity in the workplace.

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