Senior Clinical Research Associate - US - Oncology
About the role
Responsible for managing the research activities at sites participating in Worldwide’s clinical research projects. Typically involved in all stages of the clinical study, including identifying potential sites to participate in the research effort, performing various study start-up activities such as working with sites to collect appropriate regulatory documents and supporting the negotiation of contracts and budgets, training the sites to collect data properly and report any potential safety-related events, managing the site's activities during study maintenance, and closing down research activities at the sites once the study has concluded.
Responsibilities
- Conduct study initiation visits (SIVs)
- Ensure compliance with obtaining informed consent, reporting potential safety-related events, and adhering to all applicable regulatory requirements
Requirements
- Excellent interpersonal, oral, and written communication skills in English
- Superior organizational skills with attention to detail
- Ability to work with little or no supervision
- Proficiency in Microsoft Office, CTMS, and EDC Systems
Qualifications
- 5+ years of experience as a Clinical Research Associate
- 4-year university degree OR Nursing Degree
- Experience in Oncology and Rare Disease is required
- Fluent in written and verbal English required
- Candidates must reside in Brazil
- Willingness to travel regionally required
Skills
- Strong project management skills
- Knowledge of regulatory guidelines and standards
- Ability to manage multiple tasks simultaneously
- Excellent problem-solving and critical thinking skills
Benefits
At Worldwide Clinical Trials, we offer a competitive benefits package depending on location. We ensure pay equity and transparency and comply with all applicable labor laws.
Pay
The salary range for this position is annually:
- United States of America - $97,000.00 - $193,000.00
Schedule
We offer a flexible schedule to accommodate your needs.