Job Summary
The In-House Clinical Research Associate (CRA) plays a critical role in overseeing clinical trials and ensuring compliance with regulatory standards. This position primarily involves managing study protocols, monitoring trial progress, and facilitating effective communication among stakeholders. The In-House CRA is pivotal in maintaining the integrity of clinical data and ensuring that research efforts align with both the company’s objectives and industry regulations.
Responsibilities
- Oversee the planning and execution of clinical studies from initiation to completion.
- Maintain documentation and ensure adherence to regulatory guidelines and company policies.
- Monitor data collection processes to guarantee accuracy and integrity.
- Conduct site visits and maintain communication with study sites to ensure compliance.
- Support the development and training of clinical study staff.
- Assist in the analysis and reporting of clinical trial data.
Qualifications
- Bachelor’s degree in life sciences or a related field.
- Prior experience in clinical research or a similar role is preferred.
- Strong understanding of Good Clinical Practice (GCP) guidelines.
- Excellent organizational and management skills.
- Effective communication abilities, both written and verbal.
Ocugen 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.
