Job Summary
The Senior Clinical Research Associate (CRA) specializing in Oncology will oversee clinical trials within the Midwest and Central regions. This position requires a seasoned professional capable of managing trials efficiently while ensuring compliance with protocols, regulations, and quality standards. The Senior CRA will play a crucial role in coordinating with various stakeholders to facilitate the progress of oncology studies and to support patient safety and data integrity throughout the research process.
Responsibilities
- Oversee the initiation, monitoring, and closing of clinical trials in the oncology field.
- Ensure sites are compliant with regulatory requirements, Good Clinical Practice (GCP), and the study protocol.
- Conduct site visits to assess trial progress, adherence to protocols, and monitor safety and data integrity.
- Act as a liaison between sponsors, investigators, and site staff to facilitate effective communication and problem-solving.
- Review and validate data collected from clinical studies, identifying discrepancies, and ensuring high-quality data is reported.
- Provide training and support to site personnel on study protocols and procedures.
- Collaborate with cross-functional teams to enhance trial execution and patient recruitment strategies.
Qualifications
- A degree in Life Sciences, Nursing, or a related field.
- Minimum of 3-5 years of experience in clinical monitoring or related roles in the pharmaceutical or clinical research industry, particularly in oncology.
- Strong understanding of clinical trial phases, regulatory guidelines, and compliance requirements.
- Excellent communication and interpersonal skills for effective collaboration with various stakeholders.
- Ability to work independently and as part of a team while managing multiple priorities.
- Proficient in data management and familiarity with electronic data capture systems.
