Manager, Regulatory Affairs

Why Hologic

Hologic empowers people to live healthier lives everywhere, every day. We are the leading Innovator in women's health, helping healthcare professionals around the world diagnose and treat their patients with precision, certainty and confidence.

What to expect

The Manager of Regulatory Clinical Services is responsible for the strategy, execution, and adequacy of clinical evaluation (CEP/CER), post‑market clinical follow‑up (PMCF), and periodic safety update report (PSUR and/or PMSR) activities for assigned medical devices across their lifecycle. This role ensures compliance with EU MDR and other global regulatory requirements and provides clinical and regulatory leadership to support product approvals, lifecycle management, and post‑market obligations.

This position is remote

Clinical Evaluation Strategy & Oversight:

• Develop, maintain, and execute Clinical Evaluation Plans (CEP) and Clinical Evaluation Reports (CER) in accordance with EU MDR Annex XIV and MEDDEV/MDCG guidance.
• Ensure ongoing clinical evaluation is appropriate to device risk, clinical claims, and state of the art.
• Oversee literature reviews, clinical data appraisal, benefit‑risk assessments, and equivalence justifications.
• Ensure timely updates of CERs based on PMS, PMCF, vigilance, and new scientific evidence.

• Serve as clinical evaluation, post-market clinical follow-up, and periodic safety update report subject‑matter expert during Notified Body interactions, audits, and inspections.

  Post‑Market Clinical Follow‑up (PMCF)

• Define and manage PMCF strategies appropriate to device classification and residual risk.
• Oversee development and maintenance of PMCF Plans and PMCF Evaluation Reports.
• Coordinate PMCF activities including registries, surveys, observational studies, and clinical investigations, as applicable.

• Ensure PMCF outputs feed into risk management, clinical evaluation, and PSUR processes.

  Periodic Safety Update Reports (PSUR) & Post Market Surveillance Reports (PMSR)

• Oversee development and maintenance of PSURs & PMSRs. Ensure corresponding Plans are being kept current.

• Ensure PSUR outputs feed into clinical evaluation.

  Cross‑functional Leadership, People Management, & Project Management

• Collaborate with cross-functional teams including but not limited to: Regulatory Affairs, Clinical, R&D, Quality and Marketing.
• Provide training to GSS division on regulatory requirements related to Clinical Evaluations, and Post Market Clinical Follow-up activities.
• Mentor direct reports, fostering a culture of growth, accountability, and continuous improvement.

• Drive resource planning and project timelines to ensure on-time report delivery.

  Quality & Compliance

• Ensure clinical documentation meets internal procedures and external regulatory expectations.
• Contribute to SOP development and continuous improvement of clinical and PMS processes.

• Support regulatory submissions and responses to Notified Body questions related to clinical performance.

  What we expect

  Education & Experience

• Preferred Minimum Non-Technical Degree: College Degree
• Preferred Minimum Technical/Advanced Degree: Master’s degree.
• A minimum of 8 years of experience in clinical evaluations, post-market clinical follow-up and periodic safety update report activities.
• Strong working knowledge of EU MDR, clinical evaluation and PMCF requirements and global PSUR expectations.
• Experience leading people and projects with track record of successful results.

• Experience interacting with Notified Bodies.

  Skills

• Strong oral and written communication and presentation skills.
• Ability to evaluate published clinical literature.
• Knowledge and understanding of medical and clinical terminology, clinical workflow, study design, and levels of evidence.
• Demonstrated ability to coordinate complex projects.
• Firm understanding of regulatory issues in the medical device space and GCP.
• Good analytical, critical thinking and problem-solving skills.
• Demonstrate in-depth understanding of advanced technical/scientific principles related to medical device safety and performance.

• Solid computer skills in Microsoft Office.

The annualized base salary range for this role is $92,000 to $144,000 and is bonus eligible. Final compensation packages will ultimately depend on factors including relevant experience, skillset, knowledge, geography, education, business needs and market demand..

Agency and Third Party Recruiter Notice

Agencies that submit a resume to Hologic must have a current executed Hologic Agency Agreement executed by a member of the Human Resource Department. In addition Agencies may only submit candidates to positions for which they have been invited to do so by a Hologic Recruiter. All resumes must be sent to the Hologic Recruiter under these terms or they will not be considered.

Hologic, Inc. is proud to be an Equal Opportunity Employer inclusive of disability and veterans.

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