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Open nowPosted 51 days ago

Clinical Research Assistant, Brian Biesman MD

Vos Collection16 open roles

Pay
$60,000 – $65,000 a year
Where
Nashville, Tennessee, United States
Work mode
On site
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Your applicationOpen nowClinical Research Assistant, Brian Biesman MDVos Collection · Nashville, Tennessee, United States

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The clock on this job

Early applications get read.

13.9% of postings close within 7 days. Measured by our own scanner across the market. Vos Collection postings stay open a median of 33 days.

Share of postings closed within
  1. 2.2%1 day
  2. 4.7%3 days
  3. 13.9%7 days
  4. 22.4%14 days
  5. 38.1%30 days
  6. 59.0%60 days
This job: posted 51 days ago

Vos Collection median: 33 days open

The posting

Clinical Research Assistant

Brian S. Biesman, M.D. PLLC | Nashville, Tennessee

Full-Time | On-Site | Monday–Friday Salary: $60,000 - $65,000 USD

Brian S. Biesman, M.D. PLLC is seeking an experienced, highly organized Clinical Research Assistant to join our Nashville clinical research team. Our research program conducts industry-sponsored clinical trials in aesthetic medicine, including studies involving pharmaceuticals, medical devices, injectables, energy-based technologies, and other emerging treatments.

This position is ideal for someone with professional clinical research experience who is detail-oriented, accountable, and interested in developing a long-term career in clinical research.

Important: This position requires prior paid, professional clinical research experience. Academic research, college coursework, volunteer positions, and internships do not satisfy the minimum experience requirement.

Minimum Qualifications

Applicants must meet all of the following requirements:

  • Current Good Clinical Practice (GCP) certification
  • Minimum of one year of paid, professional experience as a Clinical Research Assistant or in a comparable clinical research position
  • Experience working on industry/sponsor-led clinical trials
  • Working knowledge of clinical trial protocols, source documentation, regulatory requirements, and study visit procedures
  • Strong organizational skills with exceptional attention to detail and accuracy
  • Ability to follow study protocols, recognize discrepancies or potential deviations, and escalate concerns appropriately
  • Professional written and verbal communication skills
  • Ability to manage multiple responsibilities, prioritize effectively, and meet study deadlines

Experience obtained solely through academic research, college coursework, volunteer work, or internships will not be considered toward the required one year of professional clinical research experience.

What We Are Looking For

We are looking for more than someone who can simply complete assigned research tasks. We want a motivated team member who will become an integral part of our clinical research program and grow with the position.

The successful candidate will demonstrate initiative, sound judgment, personal accountability, and consistent follow-through. They should be comfortable working independently while collaborating closely with investigators, coordinators, sponsors, monitors, research participants, and other members of the clinical team.

The ideal candidate will also have:

  • A genuine interest in clinical research and aesthetic medicine
  • Exceptional attention to detail and commitment to data accuracy
  • Strong organizational and time-management skills
  • Professional, compassionate interaction with research participants
  • The ability to anticipate study needs and take appropriate initiative
  • A commitment to protocol compliance, data integrity, participant safety, and high-quality research
  • An interest in continued professional development and advancement within clinical research

Responsibilities

The Clinical Research Assistant will work under the direction of the Principal Investigator and Lead Clinical Research Coordinator. Responsibilities will include:

  • Assist with the day-to-day conduct of industry-sponsored clinical trials
  • Review study protocols and prepare for participant visits
  • Support participant recruitment, prescreening, scheduling, and retention
  • Assist with the informed consent process within the scope of training and delegation
  • Assist with study visit procedures within the scope of training and delegation
  • Complete accurate, timely, and protocol-compliant source documentation
  • Enter study data into electronic data capture (EDC) systems and assist with resolution of data queries
  • Maintain regulatory documents, participant records, and study files
  • Track study supplies, investigational products, and study-related materials as assigned
  • Assist with site initiation visits, monitoring visits, audits, and study closeout activities
  • Communicate professionally with participants regarding appointments and study requirements
  • Help ensure that study activities are conducted according to the protocol, GCP, site procedures, and applicable regulatory requirements
  • Promptly escalate eligibility questions, protocol concerns, discrepancies, and potential deviations
  • Perform additional clinical research responsibilities as assigned and appropriately delegated

Preferred Qualifications

The following qualifications are preferred but not required:

  • Degree or certificate in life sciences, healthcare, nursing, or a related field
  • Medical Assistant, LPN, RN, phlebotomy, or other relevant clinical training
  • More than one year of professional clinical research experience
  • Experience with industry-sponsored Phase II–IV clinical trials
  • Experience with pharmaceutical, biotechnology, medical device, injectable, or aesthetic clinical trials
  • Experience with EDC platforms and electronic or paper regulatory documentation
  • Familiarity with FDA regulations and IRB requirements
  • Experience with phlebotomy, specimen collection/processing, or ECG/EKG acquisition
  • ACRP or SOCRA membership or certification

Professional Growth

This position offers meaningful opportunities for increased responsibility and professional advancement. A successful Clinical Research Assistant who demonstrates strong knowledge, judgment, initiative, reliability, and performance will have the opportunity to advance toward a Clinical Research Coordinator role.

How to Apply

Please submit a current resume that clearly describes your paid professional clinical research experience, including your experience with industry/sponsor-led clinical trials.

Candidates selected for an interview will be asked to provide proof of current GCP certification and professional references.

Application Question(s):

  • Do you have experience with EDC platforms and electronic or paper regulatory documentation?
  • Do you have experience with phlebotomy, specimen collection/processing, or ECG/EKG acquisition?
  • Please briefly describe your clinical research experience, including the types of trials you have supported (e.g., pharmaceutical, medical device, injectable, aesthetic) and any relevant clinical training or certifications.

Experience:

  • professional clinical research: 1 year (Required)
  • industry-sponsored Phase II–IV clinical trials: 1 year (Required)

Work Location: In person

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