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.
