Clinical Research Professional
6 days ago
Roles at the P21 level in Clinical Monitoring / CRA are responsible for ensuring the conduct of clinical studies according to accepted practices. These roles impact the quality and integrity of clinical research, contributing to medical advancements and patient outcomes.
- Conduct thorough on-site and remote monitoring to ensure compliance with regulatory requirements.
- Develop and implement quality tools and processes to streamline clinical trial operations.
- Manage project components within their responsibility, including site visits, study tracking, and issue resolution.
- Apply professional knowledge obtained through education and experience to maintain high standards.
- Collaborate with investigators, site staff, and stakeholders to support trial operations.
- Document monitoring activities accurately and timely, including reports and follow-up actions.
- Bachelor's degree or equivalent experience in a related field.
- 2-4 years of clinical research monitoring experience.
- Strong knowledge of GCP and regulatory requirements.
- Excellent communication and interpersonal skills.
We foster a Total Self culture where authenticity is valued, and we care for our people. We also develop our people through career growth, supportive management, training, peer recognition, and rewards.
Other InformationResponsibilities listed are not exhaustive. The company may assign other duties at its discretion. Qualifications may be considered equivalent.
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