Lead impactful clinical trials ensuring participant safety and regulatory compliance. Collaborate with multidisciplinary teams to drive trial success and innovation. Enhance professional expertise in a dynamic research environment.
Principal Investigator – Neurologist
in Healthcare + Life Sciences ContractJob Detail
Job Description
Overview
- Serve as Principal Investigator for clinical trials, ensuring adherence to ICH/FDA/GCP guidelines and local regulations.
- Provide medical oversight and ensure participant safety during clinical trial execution.
- Evaluate participant eligibility and ensure compliance with study protocols.
- Collaborate with sponsors, clients, and team members to achieve trial objectives.
- Conduct protocol training for staff and participate in Investigator Meetings.
- Maintain accurate and detailed records of participant data and study outcomes.
- Adapt to dynamic workloads and priorities while maintaining high standards.
- Ensure confidentiality and compliance with HIPAA guidelines in handling sensitive information.
Key Responsibilities & Duties
- Lead clinical trial activities, ensuring ethical execution and adherence to regulatory guidelines.
- Evaluate and enroll eligible participants, ensuring protocol compliance.
- Monitor participant safety and maintain high standards of care.
- Collaborate with multidisciplinary teams to ensure trial success.
- Provide training and guidance to staff on protocol requirements.
- Participate in Investigator Meetings and continuing education activities.
- Maintain detailed and accurate documentation of trial activities.
- Adapt to changing priorities and workloads while maintaining professionalism.
Job Requirements
- Doctor of Medicine (MD) degree with active physician license in good standing.
- Board certification in neurology and clinical research experience required.
- Proficiency in clinical procedures and computer applications, including MS Office and electronic health records.
- Strong organizational skills, attention to detail, and ability to handle sensitive information.
- Effective communication skills, both written and verbal, with bilingual proficiency preferred.
- Ability to work independently and collaboratively, adapting to dynamic priorities.
- Commitment to ethical practices and participant safety in clinical trials.
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