CRA (Clinical Research Associate) entry level

Om jobbet

Entry-Level Clinical Research Associate (CRA)

Employer: Corpremans Clinical Trial Consultancy AB

Location: Bjärred, Sweden (few days in office and few days remotely from home)

Employment type: 6 months training and then employment

Start date: As early as possible.

About the role

Corpremans Clinical Trial Consultancy AB is looking for a Clinical Research Associate (CRA) to join our team. The role is suitable for a junior or entry-level candidate interested in gaining experience in clinical research and clinical trial monitoring.

The CRA will support the management and monitoring of clinical trials to ensure compliance with study protocols, regulatory requirements, and Good Clinical Practice (ICH-GCP).

Main responsibilities

Assist with monitoring clinical trial sites (remote and on-site)

Verify clinical trial data and documentation

Support investigators and clinical trial sites

Prepare monitoring visit reports

Ensure compliance with study protocols and regulatory requirements

Maintain study documentation and trial records

Qualifications

Degree in Life Sciences, Pharmacy, Medicine, Nursing, or related field

Basic knowledge of clinical research and ICH-GCP

Good organizational and communication skills

Fluency in English and Swedish

Candidate should be based in Skåne as it is required to come to office few days a week.

Meriting

Experience in clinical research or healthcare

Knowledge of electronic data capture (EDC) systems

Understanding of EU clinical trial regulations

Other

Some travel to clinical trial sites may be required.

About Corpremans Clinical Trial Consultancy AB

We provide consulting and monitoring services for clinical trials conducted by pharmaceutical, biotechnology, and medical device companies, ensuring high-quality research and regulatory compliance.