Senior Market Access Manager

Cencora; Lombardia; On-site; EUR 65,000 - 90,000; Full time

Job summary

Cencora is seeking an experienced pharmacovigilance professional to lead client engagements and deliver safety surveillance services in Lombardy, Italy. You will coordinate case processing, ensure timely, compliant safety deliverables, and support regulatory documentation throughout the product lifecycle.

The role emphasizes mentoring junior staff and enhancing processes for quality improvement within a global pharmacovigilance framework.

Qualifications

• Bachelor's degree in life sciences or related field is required.
• Pharmacovigilance certification preferred; regulatory affairs certification preferred; quality management/auditing certification preferred.
• 4+ years of experience in pharmacovigilance, drug safety, epidemiology, risk management, or regulatory affairs is required.
• Experience with client-facing scientific consulting is a plus.

Responsibilities

• Delivers client engagements and work products related to pharmacovigilance, safety surveillance, risk management, and related scientific consulting services within defined scope, quality, and timeline expectations.
• Coordinates case processing, documentation, reporting activities, and handoffs to support compliant safety deliverables.
• Analyzes safety data and literature to support signal detection and client recommendations.
• Supports development and maintenance of risk management deliverables and regulatory documentation across the product lifecycle.
• Recommends improvements to procedures, templates, and workflow controls to enhance quality and reduce rework.
• Facilitates coordination with client stakeholders and internal partners to confirm requirements and align with service expectations.
• Guides less-experienced professionals through standards, documentation, and reusable ways of working.

Skills

Pharmacovigilance

Safety surveillance

Risk management

Regulatory compliance

Client engagement

Mentoring junior staff

Education

Bachelor’s degree in life sciences or related field

Pharmacovigilance certification

Regulatory affairs certification (clinical safety)

Quality management / auditing certification

Job description

Our team members are at the heart of everything we do. At Cencora, we are united in our responsibility to create healthier futures, and every person here is essential to us being able to deliver on that purpose. If you want to make a difference at the center of health, come join our innovative company and help us improve the lives of people and animals everywhere.

Job Details

Responsibilities:

• Delivers client engagements and work products related to pharmacovigilance, safety surveillance, risk management, and related scientific consulting services within defined scope, quality, and timeline expectations.
• Coordinates case processing, documentation, reporting activities, and operational handoffs to support accurate, timely, and compliant safety deliverables.
• Analyzes safety data, literature, and other relevant information to support signal detection, signal assessment, and fit-for-purpose client recommendations.
• Supports development and maintenance of risk management deliverables, benefit-risk assessments, and related regulatory documentation across the product lifecycle.
• Recommends and implements improvements to procedures, templates, and workflow controls that improve quality, reduce rework, and strengthen compliance within the job area.
• Facilitates coordination with client stakeholders and internal partners to confirm requirements, resolve routine issues, and maintain alignment to service expectations and controls.
• Guides less-experienced professionals through practical application of standards, documentation expectations, and reusable ways of working.

#LI-AT2

.

Education:

• Bachelor’s degree in life sciences, pharmacy, medicine, nursing, public health, epidemiology, regulatory affairs, or a related field, or equivalent experience required.
• Certification in pharmacovigilance, drug safety preferred. Certification in regulatory affairs, clinical safety preferred. Certification in quality management, auditing preferred.

Experience:

• 4+ years of experience in pharmacovigilance, drug safety, epidemiology, risk management, scientific consulting, regulatory affairs, or a related field required.

What Cencora offers

Benefit offerings outside the US may vary by country and will be aligned to local market practice. The eligibility and effective date may differ for some benefits and for team members covered under collective bargaining agreements.

Full time

Affiliated Companies

Affiliated Companies: PharmaLex Italy SPA

Equal Employment Opportunity

Cencora is committed to providing equal employment opportunity without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, age, disability, veteran status or membership in any other class protected by federal, state or local law.

The company’s continued success depends on the full and effective utilization of qualified individuals. Therefore, harassment is prohibited and all matters related to recruiting, training, compensation, benefits, promotions and transfers comply with equal opportunity principles and are non-discriminatory.

Cencora is committed to providing reasonable accommodations to individuals with disabilities during the employment process which are consistent with legal requirements. If you wish to request an accommodation while seeking employment, please call 888.692.2272 or email [e-mail]. We will make accommodation determinations on a request-by-request basis. Messages and emails regarding anything other than accommodations requests will not be returned