Clinical Research Compliance Manager

Tribeclinicalresearch

Greenville, SCFull-time

72K–108K a year

Behavioral Health Market Context

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Benefits

Paid Time Off

Job Description

al role in overseeing and ensuring that all clinical research activities comply with regulatory requirements, company policies and industry standards. This role involves managing audits, developing compliance programs, providing training to staff on all compliance related matters and acting as a key liaison between regulatory agencies and the organization.
Key Accountabilities
• Lead, Manage, Accountable – Regulatory Department
• Regulatory compliance oversight
• Audit and monitor
• Policy development and implementation
• Education and training
Qualifications & Experience
• Bachelor’s degree in a relevant field (e.g., Clinical Research, Health Sciences, or Regulatory Affairs). Advanced degree preferred.
• Minimum of 5 years of experience in clinical research or compliance, with at least 2 years in a supervisory or management role.
• Relevant certifications such as Certified Clinical Research Professional (CCRP), Certified IRB Professional (CIP), or Regulatory Affairs Certification (RAC) are highly desirable.
• In-depth knowledge of clinical research regulations, including FDA, ICH-GCP, and HIPAA requirements.
• Strong organizational and analytical skills.
• Excellent communication and interpersonal abilities.
• Proficiency in compliance management systems and Microsoft Office Suite.
• Ability to manage multiple priorities in a fast-paced environment.
Physical Requirements

Requires sitting, standing, and walking associated with a normal clinical research / physician office environment. Person may be exposed to fumes, airborne particles, infectious diseases, blood/bodily fluids, and disease-bearing specimens.

Tribe Clinical Research is an independent, faith-based, clinical research facility that conducts both adult and pediatric research studies. Our purpose is to provide hope for the future by unlocking the potential of medicine.
Our core values
• We are passionate about working for a GROWTH ORIENTED company.
• We exhibit a HUMBLE but CONFIDENT approach to work.
• We communicate RESPECTFULLY.
• We love serving others and WORKING TOGETHER for the greater good.
• We can take constructive feedback well and have a POSITIVE ATTITUDE.
Other benefits
• Excellent PTO plan including your birthday day off
• 7 paid holidays
• 401K
• $150 uniform stipend
• Monthly Phone Stipend
• Office amenities (coffee, snacks, water)
• An amazing team to work with

Tribe Clinical Research is an Equal Opportunity Employer

545 Verdae Blvd, Greenville, SC 29607, USA

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Salary: USD 72000 - 108000 per year

Qualifications

  • Bachelor’s degree in a relevant field (e.g., Clinical Research, Health Sciences, or Regulatory Affairs)
  • Requires sitting, standing, and walking associated with a normal clinical research / physician office environment

Benefits

  • Excellent PTO plan including your birthday day off
  • 7 paid holidays
  • 401K
  • $150 uniform stipend
  • Monthly Phone Stipend
  • Office amenities (coffee, snacks, water)
  • An amazing team to work with
  • Salary: USD 72000 - 108000 per year

Responsibilities

  • Tribe Clinical Research is seeking an experienced and highly organized Clinical Research Compliance Manager
  • This position plays a crucial role in overseeing and ensuring that all clinical research activities comply with regulatory requirements, company policies and industry standards
  • This role involves managing audits, developing compliance programs, providing training to staff on all compliance related matters and acting as a key liaison between regulatory agencies and the organization
  • Lead, Manage, Accountable – Regulatory Department
  • Regulatory compliance oversight
  • Audit and monitor
  • Policy development and implementation
  • Education and training
  • Person may be exposed to fumes, airborne particles, infectious diseases, blood/bodily fluids, and disease-bearing specimens


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