Clinical Research Associate (CRA) Monitor (fmd)

FGK Career

Not Interested
Bookmark
Report This Job

profile Job Location:

Guildford - UK

profile Monthly Salary: Not Disclosed
Posted on: 17 hours ago
Vacancies: 1 Vacancy

Job Summary

Your mission
  • You support project management in the planning organisation and implementation of national and international clinical trials in phases II to IV.
  • You conduct monitor visits (initiation monitoring of ongoing trial activities and close-out) in accordance with SOPs and applicable guidelines across the UK.
  • You work closely with the trial centers and the relevant departments of the sponsor.
  • You prepare study-related documents (e.g. for authorities and ethics committees) and project plans select potential trial centers prepare training courses and presentations and conduct these independently.
Your profile
  • You are a scientist physician or have a relevant qualification in the medical field.
  • It would be advantageous if you already have professional experience as a CRA or have successfully completed basic CRA training.
  • You have strong communication skills and fluency in English.
  • Additional excellent language skills and knowledge of ICH-GCP guidelines are an advantage but not a requirement.
  • You are flexible when the role requires.
  • You are organised punctual have great interpersonal skills and happy to work with the team.
  • You have an entitlement to work in the UK.
  • You have a UK drivers licence.
Why us
  • We ensure you a thorough introduction and support from a team of experienced natural scientists.
  • We offer exciting and varied projects from the pharmaceutical biotech and medical production sectors.
  • We guarantee fast decision-making processes due to flat hierarchies and open doors culture.
  • We love diversity! Our teams are diverse cross-generational and we work and learn with and from each other.
  • We have modern well-equipped offices.
  • We provide flexible home office options with a minimum of 1 day per week in the office.
We invite you to join us in making a lasting difference in the lives of countless patients. Every day anew.
Interested
We are looking forward to your application.
About us

We feel responsible.

In our medium-sized and owner-managed CRO honest and success-oriented cooperation is even more important than a company and personnel policy controlled by external capital.
If you also value long-term teamwork in a family environment with a collegial cordial and yet professional working atmosphere then you have come to the right place.



Required Experience:

IC

Your missionYou support project management in the planning organisation and implementation of national and international clinical trials in phases II to IV.You conduct monitor visits (initiation monitoring of ongoing trial activities and close-out) in accordance with SOPs and applicable guidelines a...
View more view more

Key Skills

  • CSS
  • Cloud Computing
  • Health Education
  • Actuary
  • Building Electrician

About Company

Company Logo

We feel responsible. In our medium-sized and owner-managed CRO, honest and success-oriented cooperation is even more important than a company and personnel policy controlled by external capital. If you also value long-term teamwork in a family environment with a collegial, cordial and ... View more

View Profile View Profile