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Clinical Compliance Jobs (NOW HIRING)

Eleanor Health

Director of Clinical Compliance

$81K - $111K/yr

About the Role Eleanor Health is looking for a Director of Clinical Compliance who doesn't just keep us compliant today, but sees where regulation is heading and gets us there first. This role is ...

OpenLoop Health, Inc.

$180 - $290/hr

About the Role As Senior Director, Clinical Compliance , you will own end-to-end accountability for OpenLoop's compliance program and demonstrable regulatory readiness across every regime that ...

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Solventum

Medical Writer - Clinical Compliance

$124K - $170K/yr

Medical Writer - Clinical Compliance(Solventum) 3M Health Care is now Solventum At Solventum, we enable better, smarter, safer healthcare to improve lives. As a new company with a long legacy of ...

Pacs

$90K - $120K/yr

General Purpose Reporting to the Senior Director of Clinical Audit, the Clinical Compliance Auditor II is an advanced-level compliance professional responsible for conducting comprehensive clinical ...

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Clinical Compliance information

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$31.5K

$98.9K

$207.5K

How much do clinical compliance jobs pay per year?

As of Aug 15, 2026, the average yearly pay for clinical compliance in the United States is $98,949.00, according to ZipRecruiter salary data. Most workers in this role earn between $61,500.00 and $115,000.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in clinical compliance, and why are they important?

To thrive in Clinical Compliance, you need a strong understanding of healthcare regulations, quality assurance processes, and risk management, typically supported by a degree in a health-related field or compliance certification such as CHC (Certified in Healthcare Compliance). Familiarity with regulatory databases, audit software, and documentation systems is frequently required. Attention to detail, ethical judgment, and effective communication are key soft skills for this role. These qualities ensure organizations maintain regulatory standards, minimize risks, and foster a culture of compliance.

Is healthcare compliance a good career?

Healthcare compliance is a growing field that involves ensuring healthcare organizations follow laws, regulations, and policies. It often requires knowledge of legal standards, attention to detail, and certifications such as Certified in Healthcare Compliance (CHC). The role offers stability and opportunities for advancement in the healthcare industry.

What are some typical challenges faced by professionals in clinical compliance roles?

Professionals in Clinical Compliance often face challenges such as keeping up with frequently changing healthcare regulations, navigating complex documentation requirements, and ensuring consistent adherence to compliance standards across teams. They may also encounter resistance when implementing new policies or conducting audits, requiring both persistence and strong interpersonal skills. Despite these challenges, the role offers the opportunity to make a significant impact on patient safety and institutional integrity while working collaboratively with healthcare providers, administrators, and regulatory bodies.

What is a clinical compliance?

A Clinical Compliance job involves ensuring that healthcare organizations, clinical trials, or medical practices follow regulatory guidelines, industry standards, and internal policies. Professionals in this role monitor compliance with laws such as FDA regulations, HIPAA, and Good Clinical Practice (GCP). They conduct audits, provide training, and implement corrective actions to maintain ethical and legal standards in patient care and clinical research.

What does a clinical compliance specialist do?

A clinical compliance specialist ensures that healthcare practices, procedures, and documentation adhere to regulatory standards and industry guidelines. They review clinical processes, conduct audits, and implement policies to maintain compliance, often working with electronic health records and requiring knowledge of healthcare regulations such as HIPAA or FDA requirements.
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Cities with the most Clinical Compliance job openings:

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Clinical Compliance jobs near you
Infographic showing various Clinical Compliance job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 84% Full Time, 11% Part Time, and 4% Contract. Highlights an 93% Physical, 3% Hybrid, and 4% Remote job distribution, with an average salary of $98,949 per year, or $47.6 per hour.

Clinical Compliance Manager

Neurocrine Biosciences, Inc.

San Diego, CA • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 9 days ago

Job description

Who We Are:
Neurocrine Biosciences is a leading biopharmaceutical company with a simple purpose: to relieve suffering for people with great needs. We are dedicated to discovering, developing and commercializing life-changing treatments for patients with under-addressed neurological, psychiatric, endocrine and immunological disorders. The company's diverse portfolio includes FDA-approved treatments for tardive dyskinesia, chorea associated with Huntington's disease, classic congenital adrenal hyperplasia, hyperphagia in patients with Prader-Willi syndrome, endometriosis* and uterine fibroids*, as well as a robust pipeline including multiple compounds in mid- to late-phase clinical development across our core therapeutic areas. For more than three decades, we have applied our unique insight into neuroscience and the interconnections between brain and body systems to treat complex conditions. We relentlessly pursue medicines to ease the burden of debilitating diseases and disorders, because you deserve brave science. For more information, visit neurocrine.com, and follow the company on LinkedIn, X, Facebook and YouTube. (*in collaboration with AbbVie)
About the Role:
Independently leads and collaborates with Clinical Operations (ClinOps) to drive strategic initiatives related to clinical process compliance, continuous improvement, and inspection readiness. Plays a pivotal role in shaping and implementing process enhancements, including study-specific training programs and management of NBI consent document templates. Oversees the facilitation of training and the creation and revision of controlled documents to ensure operational excellence. Serves as a key ClinOps liaison, adept at identifying procedural gaps and championing innovative solutions to enhance efficiency and effectiveness across clinical processes.
Your Contributions (include, but are not limited to):
  • Guides study teams on audit/inspection activities, offering insights on findings, and escalating issues to Clinical Compliance (CC) Director when necessary
  • Serves as the ClinOps point person, providing key advice on clinical processes and Good Clinical Practices (GCP)
  • Develops and reviews new or updated ClinOps controlled documents, coordinate input from Subject Matter Experts (SMEs), assess impact, propose implementation plans, and manage timelines
  • Leads process integration and collaboration with vendors (e.g., CROs)
  • Oversees the management and updating of NBI consent document templates and related documents
  • Collaborates with NBI Drug Safety and Pharmacovigilance (DSPV) to ensure compound risk language is accurately included in consent documents
  • Manages and oversees Study-Specific Training (SST) activities, such as maintenance SST matrix templates, processing of document submissions for SST assignments, and compliance with SST processes
  • Manages SST system solution implementation, updates and user access.
  • Manages ClinOps training activities, including developing training materials and conducting live training sessions under guidance from CC Director
  • Oversees the distribution lists (DL) management process (e.g., ensure DLs for internal distribution of safety reports are created and all applicable study team members are listed prior to the first study participant is screened)
  • Oversees ClinOps training curriculum reviews, making sure controlled documents are assigned appropriately for training based on roles and consulting with group leads when necessary
  • Participates and promotes collaboration in departmental and cross-departmental meetings, as necessary
  • Develops and maintains working relationships with other functional areas outside of Clinical Operations
  • Demonstrates knowledge of applicable regulatory requirements, and business standards
  • Constantly maintains knowledge in an on-going manner
  • Performs other duties as assigned

Requirements:
  • BS/BA degree in life science or related field AND 6+ years of experience in Clinical Compliance, Clinical Operations, or related areas within the biopharmaceutical industry. Previous experience as a Clinical Trial Associate (CRA), Clinical Trial Manager (CTM) or Clinical Research Coordinator, or equivalent, preferred OR
  • Master's degree life science or related field AND 4+ years of similar experience noted above
  • Proven expertise in audit/inspection-related activities, Good Clinical Practices (GCP), and regulatory compliance, and inspection readiness
  • Strong leadership and collaboration skills, with a track record of effectively leading and supporting cross-functional teams
  • Excellent communication and interpersonal skills, with the ability to work effectively with internal and external stakeholders
  • Extensive experience in maintaining controlled documents, managing training activities, and coordinating cross-departmental collaboration
  • Comprehensive understanding of regulatory requirements and standards in the biopharmaceutical industry, with a commitment to ongoing learning and professional development
  • Excellent organizational skills and be detail oriented
  • Proficiency in both collaborative and independent work, with the capability to mentor and lead junior team members
  • Comprehensive project management expertise, including resource allocation, timeline governance, and risk mitigation strategies
  • Excellent computer skills. Experience with Veeva Vault preferred
  • Working knowledge of Clinical Operations, specifically conducting clinical studies from start-up through close-out
  • Advanced problem-solving and analytical thinking skills
  • Ability to meet multiple deadlines, with a high degree of accuracy and efficiency

#LI-SA
Neurocrine Biosciences is an EEO/Disability/Vets employer.
We are committed to building a workplace of belonging, respect, and empowerment, and we recognize there are a variety of ways to meet our requirements. We are looking for the best candidate for the job and encourage you to apply even if your experience or qualifications don't line up to exactly what we have outlined in the job description.
The annual base salary we reasonably expect to pay is $130,800.00-$179,000.00. Individual pay decisions depend on various factors, such as primary work location, complexity and responsibility of role, job duties/requirements, and relevant experience and skills. In addition, this position offers an annual bonus with a target of 30% of the earned base salary and eligibility to participate in our equity based long term incentive program. Benefits offered include a retirement savings plan (with company match), paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage in accordance with the terms and conditions of the applicable plans.

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