Physician Assistant – Clinical Research Sub-Investigator Program (Must be a USLicensed PA)

Eximia Research; Murfreesboro (TN); On-site; USD 90,000 - 130,000; Full time

Benefits offered by this job

ICH-GCP Certification

One-on-one mentorship from experienced

Exposure to Phase I-IV clinical trials

Career advancement opportunities

Job summary

Eximia Clinical Research in Murfreesboro, TN, is seeking a Physician Assistant to join its Clinical Research Development Program. This role focuses on building a long-term career in clinical trials, with hands-on study experience and mentorship, even for PAs transitioning from traditional practice.

During training, you will complete ICH-GCP certification, perform protocol-driven assessments under supervision, and prepare you to serve as a Sub-Investigator across multiple therapeutic areas upon

Qualifications

• Master's degree in Physician Assistant studies required.
• Current NCCPA certification.
• Active Physician Assistant license in the applicable state.
• Excellent clinical assessment skills.
• Strong communication and interpersonal skills.

Responsibilities

• Perform protocol-required medical assessments under PI supervision.
• Conduct comprehensive medical histories and physical examinations.
• Evaluate participant eligibility using protocol criteria.
• Monitor participant safety and document adverse events.
• Review laboratory results and ensure accurate source documentation.
• Participate in informed consent discussions as delegated.
• Assist with protocol implementation and enrollment activities.
• Maintain compliance with study protocols and GCP.

Education

Master's degree from an accredited Physician Assistant program

Job description

Job Description

Physician Assistant - Clinical Research & Sub-Investigator Development Program

Position Summary

Eximia Clinical Research is seeking an enthusiastic, patient-focused Physician Assistant (PA) interested in building a long-term career in clinical research.

This position is designed for PAs with strong clinical skills who are looking to transition into the exciting field of clinical trials. Previous clinical research experience is not required. Through Eximia's structured Sub-Investigator Development Program, you will receive comprehensive training, mentorship from experienced Principal Investigators, and hands-on experience conducting industry-sponsored clinical trials.

Upon successful completion of the training program, you will serve as a qualified Sub-Investigator supporting multiple clinical studies across a variety of therapeutic areas.

Why Join Eximia?

At Eximia Clinical Research, we believe great Sub-Investigators are developed-not simply hired.

Our Clinical Research Development Program provides:

• Comprehensive onboarding into clinical research
• Good Clinical Practice (ICH-GCP) certification
• One-on-one mentorship from experienced Principal Investigators
• Progressive responsibility through structured training
• Exposure to Phase I-IV clinical trials
• Experience across multiple therapeutic areas
• Opportunities for career advancement within one of the nation's fastest-growing clinical research networks

Essential Responsibilities

Clinical Responsibilities

• Perform protocol-required medical assessments under PI supervision.
• Conduct comprehensive medical histories and physical examinations.
• Evaluate participant eligibility using protocol inclusion/exclusion criteria.
• Monitor participant safety throughout study participation.
• Assess and document adverse events.
• Review laboratory results and diagnostic testing.
• Provide protocol-specific participant education.
• Address participant medical concerns within scope of practice.
• Ensure participant safety remains the highest priority.

Clinical Research Responsibilities

Following completion of initial training, responsibilities will include:

• Conduct protocol-required study visits.
• Perform delegated Sub-Investigator responsibilities.
• Participate in informed consent discussions as delegated.
• Assist with protocol implementation.
• Support screening and enrollment activities.
• Complete accurate source documentation.
• Review electronic case report forms for medical accuracy.
• Participate in sponsor monitoring visits.
• Maintain compliance with study protocols and GCP.

Learning & Professional Development

Successfully complete Eximia's Clinical Research Development Program, including:

• ICH-GCP Certification
• FDA regulations governing clinical research
• Human subject protection
• Clinical trial protocol interpretation
• Adverse event assessment and reporting
• Electronic data capture systems
• Source documentation best practices
• Clinical trial participant safety
• Sponsor and CRO interactions
• Inspection readiness

Qualifications

Required

• Master's degree from an accredited Physician Assistant program
• Current NCCPA certification
• Active Physician Assistant license in the applicable state
• Excellent clinical assessment skills
• Strong communication and interpersonal skills
• Passion for learning and professional growth
• Ability to work collaboratively within a multidisciplinary team

Preferred

• Two or more years of direct patient care experience
• Primary Care, Internal Medicine, Family Medicine, Emergency Medicine, Urgent Care, Neurology, Psychiatry, Endocrinology, Gastroenterology, or similar clinical background
• Previous exposure to clinical research (preferred but not required)

Ideal Candidate

The successful candidate is someone who:

• Wants to transition from traditional clinical practice into research
• Enjoys developing long-term relationships with patients
• Has exceptional attention to detail
• Thrives in a collaborative environment
• Is intellectually curious
• Enjoys learning new therapies and disease states
• Is committed to improving future medical treatments

Career Progression

Eximia is committed to developing future research leaders.

Potential advancement opportunities include:

• Clinical Research Sub-Investigator
• Senior Sub-Investigator
• Lead Sub-Investigator
• Regional Medical Lead
• Therapeutic Area Medical Lead