Associate Director, Compliance, Investigations & Monitoring

Galderma; Miami (FL); On-site; USD 170,000 - 210,000; Full time

Benefits offered by this job

Medical Insurance

Dental Insurance

Vision Insurance

401(k) Match

Paid Time Off

Job summary

Galderma seeks an experienced compliance investigator and monitoring specialist to lead the U.S. Investigations and Monitoring program, reporting directly to the Head of U.S. Compliance and overseeing day-to-day operations.

This role drives a robust speak-up culture and proactive risk remediation. The Associate Director will collaborate with HR, Legal and partners to implement policy updates, training, and enhanced monitoring, shaping a scalable, defensible investigations framework across the

Qualifications

• JD or in-house compliance investigations experience in pharma or med device.
• 8-12 years advising life sciences on compliance matters.
• Experience designing and executing monitoring programs with data analytics.

Responsibilities

• Lead U.S. compliance investigations with structured intake, documentation, and remediation.
• Develop procedures, templates, and training for investigations program.
• Design and improve the U.S. compliance monitoring program.
• Produce dashboards and reports for leadership and governance.

Skills

Compliance investigations

Leadership

Cross-functional collaboration

Analytical thinking

Communication skills

Project management

Education

Juris Doctor (JD)

Job description

Galderma is the emerging pure-play dermatology category leader, present in approximately 90 countries. We deliver an innovative, science-based portfolio of premium flagship brands and services that span the full spectrum of the fast-growing dermatology market through Injectable Aesthetics, Dermatological Skincare and Therapeutic Dermatology. Since our foundation in 1981, we have dedicated our focus and passion to the human body's largest organ - the skin - meeting individual consumer and patient needs with superior outcomes in partnership with healthcare professionals. Because we understand that the skin, we are in shapes our lives, we are advancing dermatology for every skin story.

We look for people who focus on getting results, embrace learning and bring a positive energy. They must combine initiative with a sense of teamwork and collaboration. Above all, they must be passionate about doing something meaningful for consumers, patients, and the healthcare professionals we serve every day. We aim to empower each employee and promote their personal growth while ensuring business needs are met now and into the future. Across our company, we embrace diversity and respect the dignity, privacy, and personal rights of every employee.

At Galderma, we actively give our teams reasons to believe in our bold ambition to become the leading dermatology company in the world. With us, you have the ultimate opportunity to gain new and challenging work experiences and create an unparalleled, direct impact.

The Opportunity

Galderma seeks an experienced compliance investigator and monitoring specialist to take a leadership role in the continuous development of Galderma’s U.S. Investigations and Monitoring program. The Associate Director, Compliance Investigations & Monitoring will report directly to the Head of U.S. Compliance and will be responsible for developing, implementing, and overseeing the day-to-day operation of the investigations and monitoring program. This role is integral to the organization and serves as a key member of the Ethics & Compliance team, helping to drive a robust speak-up culture, proactive risk identification, and effective remediation.

Key Responsibilities

Lead U.S. Compliance Investigations (50%)

• Expected outcomes: Timely, consistent, fair, well-documented investigations, appropriate conclusions, root-cause considerations, and actionable remediation recommendations.
• How performed: Own program framework; coordinate with HR, Legal, and key partners; set intake, triage, scoping, documentation, and closure standards; conduct investigations (data review, interviews, evidence assessment); lead investigations readouts with senior leadership; recommend remediation.
• How performed: Independently handle varied-complexity matters; partner with Compliance Business Partners and cross-functional stakeholders to interpret policies and implement remediation (policy updates, training, coaching, enhanced monitoring).

Develop Investigations Program (procedures, documentation, and training) (15%)

• Expected outcomes: Standardized, scalable investigations capability across involved functions; improved consistency and defensibility of case files.
• How performed: Establish operating procedures and protocols aligned with Code of Conduct/global standards; develop templates and guidance; train crossfunctional colleagues on investigations process, documentation, and case management expectations.

Design and continuously improve U.S. compliance monitoring program (20%)

• Expected outcomes: Risk-based monitoring coverage of high-risk activities; early detection of issues and prevention of repeat findings.
• How performed: Build and execute monitoring plans (field rides; speaker programs; advisory boards; trainings; congresses; in-market promotional/educational events); refine methodologies and sampling.
• Identify areas of emerging risks, anomalies, and trends to prioritize areas for transactional and data-driven monitoring and analytics.

Reporting, dashboards, governance alignment, and continuous improvement (15%)

• Expected outcomes: Clear leadership visibility into metrics, trends, and remediation progress; alignment with global E&C expectations.
• How performed: Develop dashboards/reporting packages; deliver periodic monitoring reports to leadership/committees; support targeted reviews; promote strong ethics and compliance culture.

Qualifications

• Juris Doctor (JD) or in-house compliance investigations experience at a pharmaceutical or medical device company.
• 8-12 years of experience advising a pharmaceutical, biotechnology, or life sciences company on compliance matters (in-house or law firm).
• Significant experience conducting internal compliance investigations and managing investigations programs (intake, triage, case handling, reporting, remediation).
• Expertise and significant experience advising on U.S. healthcare compliance for prescription products and devices.
• Deep knowledge of pharmaceutical industry regulations and therapeutic areas, and of laws/regulations/industry guidance relevant to commercialization (including Federal Anti-Kickback Statute, False Claims Act, FDCA, OIG/DOJ guidance, PhRMA Code, U.S. state and local marketing compliance laws, and relevant enforcement actions).
• Demonstrated experience designing and executing monitoring programs and activities, including field-based monitoring and data-driven analytics.
• Strong commercial acumen and understanding of market dynamics and business culture impacts.
• Excellent analytical and critical thinking skills (large datasets, trend identification, 'big picture').
• Strong interpersonal, communication, and influencing skills; effective with senior leadership and stakeholders at all levels.
• Proven ability to manage multiple complex matters in a fast paced environment; strong project management and organizational skills.
• Ability to handle confidential information appropriately and exercise sound judgment on sensitive investigations and monitoring matters.
• Demonstrated strong commitment to compliance, ethics, and accountability.
• Ability to travel up to 30%.

Physical Requirements And Work Environment

This role requires the ability to perform standard office activities, including extended periods of computer use, participation in virtual and in-person meetings, and collaboration across teams. Depending on business needs, occasional travel may be required. Work environments and physical requirements may vary based on the requirements of the role. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of the role.

Compensation

The target base salary range for this role in Boston, MA is $170,000-$210,000 per year. This range reflects the anticipated compensation for the role. Where pay falls withing the range may vary based on many factors, including, but not limited to, job responsibilities, skills, experience, education, certifications, location and applicable geographic pay zones, market conditions, internal equity and business considerations. Compensation decisions are made based on an assessment of the candidate’s qualifications and the totality of relevant factors.

In addition to base salary, this role is eligible to participate in an annual short-term incentive program, subject to plan terms and eligibility requirements.

Benefits

Galderma offers a competitive and comprehensive benefits program, including medical, dental, and vision coverage, a 401(k) plan with employer match, paid time off, and other benefits, subject to eligibility and applicable plan terms.

Work Authorization

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the United States.

What We Offer

At Galderma, you’ll be part of a purpose-driven organization committed to advancing dermatology and improving patient outcomes worldwide. We offer competitive compensation, annual incentive opportunities, and comprehensive benefits, along with meaningful opportunities for growth, development, and collaboration in an inclusive and innovative environment.