Principal Investigator (Virtual)

We are seeking a highly skilled and experienced virtual Principal Investigator to join our team. As the Principal Investigator, you will be responsible for oversight of all clinical trials according to study protocols, company processes, and GCP. Please note this is a part-time role.

Provide overall medical oversight and medical review of protocols in conformance with good clinical practice

Review sponsor provided safety reports.

Review and maintain accurate case report forms.

Ensure that the safety and well-being of all participants in the study at the trial site are protected

Assess subject response to therapy, evaluate and address adverse experiences

Perform physical assessments, examinations and study procedures as required by study protocols

Train Sub-Investigators and study staff members on protocol and protocol specific procedures. Provide medical support to sub-investigators and study staff for protocol-related issues including protocol clarifications, inclusion/exclusion determinations, and issues of patient safety and/or eligibility.

Review the inclusion/exclusion criteria, endpoint criteria, and investigational product use with the internal research team.

Complete the necessary Care Access and protocol specific trainings

Comply with ICH GCP (International Conference on Harmonization – Good Clinical Practice) and all applicable regulatory requirements

Participate in monitoring visits and sponsor meetings; allow monitoring and auditing by sponsors and inspection by appropriate regulatory agencies

Excellent written and verbal communication skills

Ability to effectively prioritize tasks in a fast-paced environment

Attention to detail and ability to maintain confidentiality when handling sensitive information.

Critical thinking, dynamic problem-solving skills

Minimum Education:

MD or DO with an active, unrestricted medical license (medical license must be valid in the state in which the research is conducted)

Minimum Experience:

Previous experience as a Principal Investigator is required; 2 years prior experience as a Principal Investigator or Sub-Investigator, preferred

Training and certification in Good Clinical Practice (GCP)

Location: Remote within the United States. This role requires 100% of work to be performed in a remote office environment.

Travel: This is a remote position with less than 10% travel requirements. Occasional planned travel may be required as part of the role.

Physical demands associated with this position Include: The ability to use keyboards and other computer equipment.

The expected pay range for this role is $200,000 - $400,000 USD per year for full time team members.

Paid Time Off (PTO) and Company Paid Holidays

100% Employer paid medical, dental, and vision insurance plan options

Health Savings Account and Flexible Spending Accounts

Bi-weekly HSA employer contribution

Company paid Short-Term Disability and Long-Term Disability

401(k) Retirement Plan, with Company Match

#LI-Remote

Diversity & Inclusion

We work with and serve people from diverse cultures and communities around the world. We are stronger and better when we build a team representing the communities we support. We maintain an inclusive culture where people from a broad range of backgrounds feel valued and respected as they contribute to our mission.

We are an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to, and will not be discriminated against on the basis of, race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, genetic information, protected veteran status, or any other characteristic protected by law.

Care Access is unable to sponsor work visas at this time.

If you need an accommodation to apply for a role with Care Access, please reach out to: [email protected]