Arbetsbeskrivning

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

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