Clinical Research Associate (m/f/d) - UK

Optimapharm; London; Remote; GBP 40,000 - 55,000; Full time

Job summary

A leading global CRO is seeking an experienced Clinical Research Associate (CRA) to join their UK team. This role involves independent monitoring of clinical trials, ensuring compliance, and collaborating with site personnel. The successful candidate will benefit from opportunities for professional growth and participation in international projects.

Benefits

Performance bonus

Training opportunities

Qualifications

• At least 2-3 years of independent clinical trial monitoring experience.
• Ability to read, analyze, and interpret scientific and technical journals.

Responsibilities

• Perform routine site visits independently, including pre-study and closeout visits.
• Manage assigned sites to ensure compliance and adequate enrollment.
• Negotiate study budgets with investigators/institutions.

Skills

Fluent in English

Strong knowledge of ICH GCP Guidelines

Excellent verbal and written communication skills

Good interpersonal and negotiation skills

Ability to work independently

Proficiency in computer skills

Education

University degree in medical or life sciences

Nursing education or relevant healthcare college degree

Job description

Location: home-based

Who we are?

Optimapharm is a globally operating, leading, mid-sized, full-service CRO aiming to deliver new therapies to improve and save patients’ lives.

Optimapharm’s key priorities are the well-being of our people, consistent quality delivery to our clients, and healthy, sustainable growth.

With 26 strategically located offices, Optimapharm operates in 40+ countries, providing optimal access to Patients and Investigators globally. Established nearly 20 years ago, we leverage our experience, stable project teams, and a collaborative, flexible approach to secure a high level of repeat business, gain the trust of new customers, and support the continued growth of the company.

We are looking for an experienced CRA to join our team in the UK and support us in making a tangible difference to project sponsors, patients, and their families worldwide.

What do we offer?

• Working in a successful company that’s growing and evolving daily
• Collaborating with a highly experienced team of clinical research professionals
• Participation in international projects and opportunities for professional growth
• Performance bonus
• Training opportunities

Who are we looking for?

Qualifications and Experience

• University degree, preferably in medical or life sciences; nursing education or relevant healthcare college degree
• At least 2-3 years of independent clinical trial monitoring experience
• Strong knowledge of ICH GCP Guidelines, regulatory requirements, and a keen interest in clinical research
• Fluent in English, both written and spoken
• Proficiency in computer skills
• Ability to read, analyze, and interpret scientific and technical journals
• Excellent verbal and written communication skills
• Good interpersonal and negotiation skills
• Ability to work independently and proactively
• Ability to work effectively in a matrix environment
• A current, valid driver’s license

Your Responsibilities

• Perform routine site visits independently, including pre-study, initiation, interim monitoring, and closeout visits
• Manage assigned sites through regular contact with site personnel to ensure compliance, adequate enrollment, and understanding of study requirements
• Review CRFs, generate queries, and resolve them according to data review guidelines or data management systems
• Identify and escalate potential risks and training needs for site personnel
• Prepare CAPA plans for issues identified during monitoring and follow up until resolution
• Prepare documents for EC submissions, translations, and other tasks as instructed
• Negotiate study budgets with investigators/institutions and assist with site contracts
• Administer site payments per project instructions

By joining our fast-growing team, you will have excellent opportunities for personal growth and career development.

If interested, please send your CV in English. Only shortlisted candidates who meet the requirements will be contacted for further steps.