Senior CRA

This is a fully remote position, open to applicants in Norway.

📋 Description

• Conduct qualification visits, site initiation visits, monitoring visits, and termination visits at designated clinical sites.

• Create visit and contact reports.

• Establish and maintain relationships with clinical sites and personnel.

• Address and resolve site-related inquiries and concerns as the primary point of contact.

• Ensure study integrity while fostering strong rapport with sites.

• Review trial performance and protect the rights and well-being of human subjects.

• Collaborate with clinical sites to devise patient recruitment strategies that align with enrollment timelines.

• Ensure adherence to SOPs, protocols/amendments, GCP, and relevant regulatory standards.

• Assess the quality and integrity of reported data, site effectiveness, and drug accountability.

• Oversee the completeness and quality of regulatory documentation.

• Conduct verification of site documents.

• Manage site quality and performance from identification through to close-out.

⛳️ Requirements

• Proven experience as a Clinical Research Associate.

• Outstanding interpersonal, verbal, and written communication abilities.

• Proficient in Norwegian.

• Good proficiency in Swedish and Danish.

• Possess a degree in biological science, pharmacy, or a related health field, or an equivalent nursing qualification or relevant experience.

• Familiarity with clinical research principles.

• Compliance with GCP, applicable regulatory standards, protocols/amendments, and standard operating procedures.

🏝️ Benefits

• Access to world-class technology and training tailored to individual experience.

• Reduced travel requirements and a lower protocol load compared to industry standards.

• Participation in a bonus incentive program.

• Opportunities to work across various therapeutic areas.

• Career progression opportunities within clinical research.

• Flexible work arrangements.