Job Summary:
We are seeking a motivated and detail-oriented Junior Research Coordinator to join the Lifedoc Health team. The Junior Research Coordinator supports clinical research activities while ensuring adherence to protocols and regulatory requirements.

Essential Duties and Responsibilities:

· Responsible for assisting in the coordination and execution of clinical trials.

· Ensuring compliance with protocols and maintaining accurate records.

· Assist with study coordination, patient interaction, documentation, and collaboration with sponsors and regulatory bodies.

· Will monitor that all patients enrolled in research who are Lifedoc’s patients will have their regular clinic follow up appointments with their medical providers and that all protocols for in clinic patients are up to date.

· In coordination with the Clinical supervisor (QI clinician) will maintain a data base of existing research and in clinic Lifedoc patients to maintain adequate care coordination and monitor clinical metrics

Clinical Responsibilities:

· Engage in patient recruitment efforts through various channels.

· Contact potential subjects and schedule appointments for screening and enrollment.

· Obtain informed consent from participants according to protocol requirements.

· Review patient searches and outreach strategies to identify eligible participants.

· Manage lab draws, processing, and shipping according to protocol.

· Conduct EKG assessments.

· Navigating EMR.

Study Coordination:

· Document patient visits and maintain accurate records.

· Conduct study visits in accordance with protocols and SOPs.

· Perform study activities as outlined in the protocol.

· Maintain contact with CRAs as needed.

· Schedule and coordinate monitor visits as required.

· Manage data entry in Clinical Trial Management System (CTMS).

· Log adverse events (AE) and ensure timely reporting.

· Conduct accountability checks and ensure timely signatures and lab uploads.

· Manage study supplies, drug dispensation, and inventory.

· Ensure drug/investigational product (IP) accountability throughout the study.

Education and Skills:

· High school diploma required; bachelor's degree in a relevant field (preferred).

· Experience in the medical field as a Medical Assistant or Nurse and exposure to research is highly preferred.

· GCP certification or relevant certifications are preferred.

· Bilingual in both English and Spanish preferred

· Strong organizational and communication skills and paying attention to detail.

· Attention to detail and ability to adhere to protocols and regulations.

· Proficiency in data management and documentation systems.

· Ability to work effectively in a multidisciplinary team.

· Knowledge of clinical research principles and practices.

· Familiarity with GCP guidelines and regulatory requirements.

Job Type: Full-time

Pay: $38,480.00 - $43,680.00 per year

Benefits:

• 401(k)
• 401(k) matching
• Dental insurance
• Employee assistance program
• Employee discount
• Health insurance
• Health savings account
• Life insurance
• Paid time off
• Referral program
• Vision insurance

Experience level:

• 1 year

Schedule:

• 8 hour shift
• Monday to Friday

Ability to Commute:

• Memphis, TN 38115 (Required)

Ability to Relocate:

• Memphis, TN 38115: Relocate before starting work (Required)

Work Location: In person