First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

Message

First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

Message

First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

Message

First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

Message

One of the largest CROS in the global market is currently recruiting a Senior CRA to their UK team on a home-based capacity. This contract research organisation (CRO) is renowned for their work in technological advances and access to real-world data. This is an exciting opportunity to become embedded in the wider clinical operations team and work on ground-breaking new medicine development.

The position will be filled at CRA or Senior CRA level depending on experience and may include customer-managed clients.

Job Responsibilities:

Monitoring activities at clinical study sites to assure adherence to Good Clinical Practices (GCPs), SOPs, and study protocols.
Reviewing regulatory documents as required and prepare site visit reports.
Participating in the study development and start-up process, including reviewing protocols, designing and/or reviewing CRFs, preparing Informed Consent forms, developing study documents, organizing and presenting at investigator meetings, working with management on monitoring strategy, and/or developing project specific CRA training.
Participating in clinical training programs and maintaining awareness of developments in the field of clinical research as needed.

Skills and Requirements:

A BS/BA degree.
2 years of monitoring experience or combination of on-site monitoring and clinical research coordinator experience.
Sound knowledge of medical terminology and clinical monitoring processes.
In-depth therapeutic and protocol knowledge as provided in company training.
Ability to perform regionalized travel an average of 65%, depending on project needs.
In depth therapeutic and protocol knowledge as provided in company training.
Demonstrable multitasking, project management, and execution skills.
Good interpersonal skills, including communication, presentation, persuasion, and influence.
Good organisational skills, including efficiency, punctuality, and collaboration in a team environment.
Proficiency with computer skills, such as MS Office.

To Apply:

Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.

In case you have difficulty in applying or if you have any questions, please contact Andrea Rotmistrovsky at +44 203 854 0675 or upload your CV on our website - www.proclinical.com.

A full job description is available on request.

ProClinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

#LI-AR1

#ClinicalResearch