Clinical Research Associate I

Experience level: mid senior level.

As a Clinical Research Associate I you will work on the frontline of communication with project stakeholders, ensuring timelines, targets and standards of clinical research projects in a variety of therapeutic indications.  You will build and maintain relationships with clinical sites and investigators.  You will focus on subjects’ rights, safety and well-being and quality of data compliance.

You will

• Conduct and report all types of onsite monitoring visits

• Be involved in study startup (if applicable)

• Perform CRF review, source document verification and query resolution

• Be responsible for site communication and management

• Be a point of contact for in-house support services and vendors

• Communicate with internal project teams regarding study progress

• Participate in feasibility research

• Support regulatory team in preparing documents for study submissions

• College/University degree in Life Sciences or an equivalent combination of education, training & experience

• Clinical Research or Medical experience

• Independent on-site monitoring experience in the UK

• PC skills to be able to work with MS Word, Excel and PowerPoint

• Ability to plan, multitask and work in a dynamic team environment

• Communication, collaboration, and problem-solving skills

• Ability to travel

• Valid driver’s license

Become a full-fledged clinical research professional with the support of a knowledgeable and professional team.  You will develop a variety of skills while progressing with the company and contributing to our full-scale challenging projects.

We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do.  A dynamic, global company founded in 1995, we bring together more than 3000 driven, dedicated and passionate individuals.  We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.