You will conduct remote or on-site visits to assess protocol and regulatory compliance while managing required documentation for top pharmaceutical companies
Job Summary
You will conduct remote or on-site visits to assess protocol and regulatory compliance while managing required documentation for top pharmaceutical companies.
The role requires applying root cause analysis and problem-solving skills to identify site process failures and ensure data accuracy through SDR and SDV reviews.
As a Clinical Research Associate Level II, you will maintain regular contact with investigative sites to confirm protocol adherence and resolve identified issues expeditiously.
Matching Summary
You will conduct remote or on-site visits to assess protocol and regulatory compliance while managing required documentation for top pharmaceutical companies.
Salary
Not specified; Not specified; Not specified
Skills & Requirements
Must-have
Bachelor's degree in life sciences
1 year clinical research monitor experience
Valid driver's license
ICH-GCP guidelines knowledge
Risk-based monitoring approach
Root cause analysis skills
Nice-to-have
Strong critical thinking abilities
Excellent oral and written communication
Collaborative team player mindset
Adaptable to remote and on-site work
Fluent Swedish language skills
Key Requirements
Bachelor's degree in life sciences or nursing certification
Minimum 1 year experience as a clinical research monitor
Valid driver's license where applicable
Completion of PPD Drug Development Fellowship (alternative)