Job Summary
The In-House Clinical Research Associate plays a crucial role in supporting clinical trial operations within the organization. This position emphasizes ensuring compliance with regulatory standards and facilitating the smooth execution of clinical research initiatives.
Responsibilities
- Manage clinical trial documentation and ensure accuracy and completeness.
- Assist in the preparation, submission, and maintenance of regulatory documents.
- Coordinate monitoring visits and ensure that study protocols are implemented correctly.
- Collaborate with cross-functional teams to maintain project timelines.
- Provide training and support to study staff on clinical protocols and procedures.
- Participate in data entry and analysis for clinical trial metrics.
- Conduct site visits to ensure compliance and adherence to study protocols.
Qualifications
- Bachelor’s degree in life sciences, nursing, or a related field.
- Prior experience in clinical research or a related field is preferred.
- Strong understanding of Good Clinical Practice (GCP) and regulatory requirements.
- Excellent organizational skills and attention to detail.
- Proficient in data management and analysis tools.
- Strong communication skills, both verbal and written.
- Able to work collaboratively in a team environment and independently.
TRI provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
