Job Summary
The Sr. Clinical Research Associate (Sr. CRA) will play a pivotal role in overseeing and coordinating the clinical aspects of our diverse range of peptide drug developments. This position is based in South San Francisco, California, and entails active onsite involvement. The Sr. CRA is responsible for managing the Investigational Product (IP) at both the study and site levels, ensuring that shipments are handled efficiently and reconciled accurately throughout the clinical study.
Responsibilities
- Independently oversee all clinical operations related to peptide drug trials.
- Ensure proper management of Investigational Product shipments and reconciliation at the level of study sites.
- Work closely with cross-functional teams to support the clinical research process.
- Monitor trial progress and ensure adherence to regulatory requirements and study protocols.
Qualifications
- Proven experience in clinical research, particularly in the role of a Clinical Research Associate.
- Strong understanding of clinical trial regulations and procedures.
- Excellent organizational, communication, and problem-solving abilities.
- Ability to work independently and as part of a broader team in a fast-paced environment.
