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Rems Associate Director Jobs (NOW HIRING)

Alexion Pharmaceuticals, Inc.

The Associate Director, Safety Scientist plays a pivotal role within Global Patient Safety ... REMS documents * Assisting GPS Medical Directors in the development of risk management strategy

Spectraforce Technologies

Telehealth Nurse

Cary, NC · On-site

The Clinical CaseRisk Evaluation and Mitigation Strategy (REMS) Clinical Nurse Educator is an ... Associates, Bachelor or higher degree in Nursing or accredited nursing diploma * Ability to obtain ...

Biogen

Sr Pharmacovigilance Scientist

Cambridge, MA · On-site

$141K - $188K/yr

Collaborating with the Associate Director, you will also hire, train, and mentor staff dedicated to ... Finalize aggregate safety reports such as PSURs, DSURs, REMS, and RMPs for assigned products.

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As of Sep 15, 2026, the average yearly pay for rems associate director in the United States is $102,728.00, according to ZipRecruiter salary data. Most workers in this role earn between $70,000.00 and $141,000.00 per year, depending on experience, location, and employer.

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Infographic showing various Rems Associate Director job openings in the United States as of June 2026, with employment types broken down into 1% Internship, 8% As Needed, 74% Part Time, 6% Temporary, 7% Contract, and 4% Nights. Highlights an 93% Physical, 1% Hybrid, and 6% Remote job distribution, with an average salary of $102,728 per year, or $49.4 per hour.

Associate Director, GVP Compliance

Remote

BioMarin Pharmaceutical Inc.
Biotechnology Research and Development • 1 - 5K employees
Learn more about BioMarin Pharmaceutical Inc.external

Full-time

Re-posted 12 days ago

BioMarin Pharmaceutical rating

7.8

Company rating: 7.8 out of 10

Based on 8 frontline employees who took The Breakroom Quiz

Job description

Who We Are
BioMarin is a leading rare disease biotechnology company focused on genetically defined conditions.
Guided by our purpose to develop medicines that make a profound impact on people’s lives, our global teams have delivered a portfolio of therapies since our founding in 1997. Our revolutionary treatments for conditions like achondroplasia (the most common form of dwarfism), PKU (phenylketonuria), CLN2, a form of Batten disease, and a number of forms of MPS (mucopolysaccharidosis) offer new possibilities for patients and families who previously had few, if any, available options. More recently, with the close of the Amicus acquisition, our portfolio has expanded to include therapies for Fabry disease and Pompe disease, expanding our ability to reach more people living with rare genetic conditions.
Our success comes from our unwavering commitment to excellence, our deep understanding of patient needs, our scientific expertise, and our world-class manufacturing capabilities. At the heart of BioMarin is a dedicated team of the brightest minds in the industry working together to deliver innovative therapies to patients and families around the world.
About Technical Operations
BioMarin’s Technical Operations group is responsible for creating our drugs for use in clinical trials and for scaling production of those drugs for the commercial market. These engineers, technicians, scientists and support staff build and maintain BioMarin’s cutting-edge manufacturing processes and sites, provide quality assurance and quality control to ensure we meet regulatory standards, and procure the needed goods and services to support manufacturing and coordinating the worldwide movement of our drugs to patients.

SUMMARY 
BioMarin is a world leader in delivering therapeutics that provide meaningful advances to patients who live with serious and life-threatening rare genetic diseases. To support this important mission, we are looking for an individual with experience working in Pharmacovigilance (PV) within the space of Quality and Compliance.  This important role will be joining our Global Quality organization and reports into the GVP Compliance Lead.
 
This role advises internal and external key stakeholders on Good Pharmacovigilance Practices (GVP) matters and assesses compliance with global regulations/guidelines, corporate policies, and standard operating procedures. This individual will perform GVP audits and act as a key point of contact supporting the readiness and execution of GVP regulatory inspections and identifies and works in partnership with stakeholders to resolve regulatory compliance risks and related issues. 
BioMarin is a global, high-performing, team-based organization, where colleagues are flexible, multi-skilled and empowered to make decisions. A high level of initiative, clear communication, effective collaboration, strategic thinking and strong decision making are important skills the candidate would possess.
 
Candidates must adhere to established processes and policies, demonstrating professionalism and integrity in all situations. They should ensure patient safety in pharmaceutical practices through a comprehensive strategy that integrates regulatory compliance, risk management, pharmacovigilance, and continuous improvement.
 
RESPONSIBILITIES 
 
  • Advancing the execution of the Global Quality vision, policies, processes, and decisions
  • Collaborate with stakeholders to identify, communicate, and mitigate compliance risks
  • Continually enhance partnerships with key stakeholders and leaders across the business
  • Support and drive the implementation of quality and compliance projects and objectives
  • Stay updated on regulations and recommend proactive compliance changes when necessary
  • Execute against GVP Compliance processes and best practices
  • Perform GVP audits and contribute to the effective implementation of the Global GVP Audit Program
  • Act as a GVP compliance core team member on regulatory inspection teams and support mock readiness activities
  • Provide insights to continually optimize the GVP Compliance Audit Program
  • Contribute to Pharmacovigilance System Master File (PSMF) updates
  • Contributor to the Risk Evaluation and Mitigation Strategies (REMS) compliance program
  • Contribute to building a team that ensures GVP compliance and foster a culture of teamwork and mutual respect
  • Mentor and support the development of junior staff to achieve their full potential
 
EXPERIENCE
 
Required Skills:
 
8+ years of experience working within a regulated healthcare industry including a role in capacity of quality and compliance
 
  • Working knowledge of FDA, EMA, and global PV Regulations, and application of Good Pharmacovigilance Practices (GVP), ICH and GCP regulations
  • Experience working in Pharmacovigilance (PV) within Quality and Compliance
  • Experience executing or managing Health Authority Inspections
  • Experience executing or managing R&D Audits and GVP Audit Program
  • Experience with identifying optimal strategy for executing a GVP audit program working with internal auditors and external consultants
  • Experience navigating and understanding a quality management system
  • Core competencies in strategic thinking, agility, prioritization, communication and decision making
  • Strong verbal, written and oral communication skills.  Able to present to Senior Leadership.
  • Able to work independently and be flexible to rapidly changing priorities
  • Strong computer skills including working within the MS Suite of tools, and interfacing with Quality Management Systems
 
Desired Skills:
 
  • Experience with Business Development partnerships, mergers and/or acquisitions
  • Exposure to working in any phase of pharmaceutical drug development or post-marketing surveillance of medicines
  • Awareness and understanding of core PV responsibilities i.e., risk management, risk minimization measures, signal management, and case processing
  • Compliance oversight of REMS Program(s)
 
EDUCATION
 
Bachelor’s Degree within a life science focus area, master’s degree is a plus
 
TRAVEL REQUIRED 
 
May travel up to 25%+ of the time
 
Equal Opportunity Employer/Veterans/Disabled
An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability.

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