Endocrinologist - Clinical Research Investigator
Endocrinologist - Clinical Research Investigator
Posted yesterday
SENIORITY
Senior
About the role
- Serve asPrincipal Investigator or Sub-Investigatoron multiple Phase I–IV clinical trials.
- Perform comprehensive physical exams and clinical assessments for protocol screening and enrollment.
- Evaluate patient eligibility based on inclusion/exclusion criteria of clinical protocols.
- Provide medical oversight for clinical trial participants, including safety assessments, adverse event evaluations, and ongoing care.
- Collaborate closely with Clinical Research Coordinators, Sponsors, and Monitors to ensure protocol compliance and data integrity.
- Review and sign off on source documents, case report forms (CRFs), and regulatory documentation.
- Maintain detailed and accurate clinical trial documentation in compliance withICH-GCP, FDA, and sponsor requirements.
- Participate inSite Initiation Visits (SIVs) , Monitoring Visits, and
- Auditsas needed.
- Manage chronic and acute conditions among study participants in alignment with standard care and protocol guidelines.
- Educate and counsel patients on study procedures, informed consent, and potential side effects.
- Support recruitment efforts and promote patient retention in trials.
Before you apply
Applying takes about a minute. These four things decide how fast it moves after that.
Your profile is current
It's what we read first. Occupations, seniority and locations matter more than a long history.
Two examples you can talk through
Not a portfolio — just two pieces of work where you can explain the decisions and what you'd change.
A number in mind
What you're on now and what would make you move. We negotiate better when we know both.
Your notice period
Employers plan around it, and it's the question that stalls offers most often.
Once you apply, someone reads it and calls you before anything reaches the employer — usually within two working days.
