Clinical Research Associate (CRA) Monitor (fmd)

FGK Career; Guildford; Hybrid; GBP 80,000 - 100,000; Full time

Job summary

A leading clinical research organization based in Guildford is seeking a qualified candidate to support project management in the planning and implementation of national and international clinical trials. Responsibilities include conducting monitor visits, preparing study-related documents, and collaborating with trial centers. The ideal candidate should possess a relevant qualification in the medical field, excellent interpersonal skills, and be entitled to work in the UK. The company offers a supportive environment and exciting projects in the pharmaceutical sector.

Benefits

Flexible home office options

Support from experienced scientists

Modern office environment

Qualifications

• You are a scientist, physician, or have a relevant qualification in the medical field.
• Professional experience as a CRA or completion of basic CRA training is advantageous.
• You have entitlement to work in the UK.
• You possess a UK driver's license.

Responsibilities

• Support project management in national and international clinical trials.
• Conduct monitor visits complying with SOPs and guidelines in the UK.
• Prepare study-related documents for authorities and ethics committees.

Skills

Strong communication skills

Fluency in English

Knowledge of ICH-GCP guidelines

Organisational skills

Interpersonal skills

Education

Relevant qualification in the medical field

Tools

Project management tools

Job description

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

Key Skills

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

Employment Type : Full-Time

Experience : years

Vacancy : 1