Responsibilities:
- Obtain and maintain essential documentation in compliance with ICH-GCP, TFS procedural documents, and local regulations.
- Actively participate in local study team meetings and contribute to the selection of potential investigators.
- Train, support, and advise investigators and site staff in study-related matters.
- Initiate, monitor, and close study sites in compliance with TFS procedural documents.
- Manage study supplies and oversee data query resolution by the site.
- Prepare for activities associated with audits and regulatory inspections.
Requirements:
- Bachelor’s Degree, preferably in life science or nursing; or equivalent.
- Previous experience as CRA including relevant independent on-site monitoring.
- Study experience in Oncology, Cardiovascular, Renal and Metabolism, Respiratory or Immunology.
- Ability to work independently and in a team matrix organization.
- Excellent written and verbal communication skills.
- Open to the possibility of national travel.
What We Offer:
- Competitive compensation package and benefits.
- Opportunity for personal and professional growth in a rewarding environment.
- Global exposure with a team of highly intelligent, passionate experts.
More Information
- Experience Level Junior
- Total Years Experience 0-5
- Radio field Option 1
- Dropdown field Option 2
- Multiple Select field Option 3
- Checkbox field Option 2
