Clinical Research Advanced Practice Provider/Sub-Investigator
Job Locations
US-MI-Plymouth
ID
2026-6306
Category
Biosciences
Position Type
Temporary Part-Time
Worker Type
Hybrid
Overview
SRI's Clinical Trials Unit is seeking an experienced Advanced Practice Provider (APP) for a part-time, temporary role in clinical research. The APP will support research studies as a Sub-Investigator, working within established study protocols in collaboration with the Principal Investigator and research team.
This role is located in Plymoth, MI, offers a high level of schedule flexibility, with work driven by study activity and planned visits.
Responsibilities
This Role Is a Good Fit for Someone Who:
Is looking for flexible, project-based work rather than a traditional PT or FT schedule
Wants research-focused work that is protocol-driven and structured
Is available for pre-scheduled, on-site study visits, with advance notice whenever possible
Is open to a mix of on-site and remote study-related work
Values predictable expectations while maintaining control over their schedule
Wants meaningful research involvement while balancing family, personal, or other professional commitments
Is dependable, responsive, and comfortable supporting studies as needs arise
Estimated Time Commitment:
Flexible, study-driven hours that vary week to week
Time commitment may be lighter at first, with an average of up to ~4-8 hours per week initially, and the potential to grow to ~8-16 hours per week as studies expand
Some weeks may be lighter, while others may be busier depending on visit schedules
On-site time scheduled in advance for study visits, with some work able to be completed remotely
As our clinical research portfolio continues to grow, there may be an opportunity for this role to transition into a more regular part-time or full-time position in the future, should there be mutual interest.
Key Responsibilities include:
Perform protocol-required Sub-Investigator duties under the direction of the Principal Investigator (PI), including medical oversight and delegated regulatory responsibilities.
Conduct comprehensive participant evaluations, including medical history review, physical examinations, and protocol-specific clinical assessments.
Determine participant eligibility based on inclusion/exclusion criteria and clinical judgment, as delegated by the PI.
Review, interpret, and assess clinical significance of laboratory results, imaging, ECGs, and other study-required diagnostics.
Provide ongoing safety oversight, including identification, evaluation, documentation, and management of adverse events and serious adverse events.
Administer study interventions and treatments in accordance with protocol requirements, clinical standards, and regulatory guidelines.
Provide study-related clinical consultations and participant education, as required by protocol.
Participate in clinical decision-making related to protocol deviations, safety concerns, and study-related medical issues, in collaboration with the PI and sponsor.
Ensure all clinical activities are conducted in strict accordance with study protocols, GCP, and applicable regulatory and institutional requirements.
Maintain accurate and complete clinical documentation, including source documentation, adverse event reporting, and case report form (CRF) review.
Review and document study data to support monitoring visits, audits, and regulatory inspections.
Collaborate with study monitors, sponsors, and internal teams to address clinical queries and ensure data integrity.
Work closely with the site team to support study execution, including clinical input for screening, enrollment, and follow-up activities.
Serve as a clinical liaison between research participants, investigators, sponsors, and healthcare providers to support participant safety and study quality.
Provide clinical oversight, mentorship, and guidance to research staff, as appropriate.
Contribute clinical expertise to the development and refinement of study protocols, SOPs, and quality improvement initiatives.
Attend required study meetings, sponsor training, and investigator meetings.
Maintain clinical licensure and stay current with regulatory requirements and industry best practices.
Qualifications
Required:
Current license to practice as an NP/PA in the state of MI
No prior sanctions by a state licensing agency; not disqualified from or restricted in the participation of clinical research by FDA
At least 3 years of experience as a provider within the healthcare industry in the US, such as a clinic, hospital, ER or other medical office setting
Past or current experience as a Sub-Investigator in commercial clinical trials
Proficiency in procedures like EKG, phlebotomy, and injections/IVs
Experience with ordering labs and lab processing
Expertise in primary care, acute care, and chronic care practices
Knowledge of health and patient care regulations
Certified in BLS and/or Advanced Cardiac Life Support (ACLS)
2-3 years of experience conducting clinical trials (federal or commercial, experience in both is a bonus)
Compliant with Good Clinical Practices (GCPs)
Candidate Traits:
Excellent clinical and communication skills
Able to make medical decisions in a fast-paced environment
Strong understanding of regulatory requirements, principles of Good Clinical Practice (GCP), and biomedical research ethics
Proficiency in electronic medical record systems and Microsoft Office Suite
Strong interpersonal and leadership skills, self-motivation, and high personal integrity
Ability to manage multiple tasks and prioritize... For full info follow application link.
SRI is an Equal Opportunity Employer, making decisions without regard to race, color, religion, creed, sex, sexual orientation, gender identity, marital status, national origin, age, veteran status, disability, or any other protected class.
