PV Drug Safety Consultant

intellipro; Cambridge (MA); Hybrid; USD 90,000 - 129,000; Full time

Benefits offered by this job

Comprehensive benefits

Job summary

IntelliPro in Cambridge, MA is seeking a PV Drug Safety Consultant to manage global aggregate reporting for PSURs, DSURs, PADERs and local reports. This hybrid role supports cross-functional safety activities and ensures high-quality PV documentation.

You will collaborate with PV Scientists, Regulatory, and external vendors to maintain compliant processes and master schedules while supporting process improvements across the PV organization.

Qualifications

• Bachelor’s degree in biological or natural sciences required.
• Advanced degree (MS/PhD/MPH/PharmD) preferred.
• Minimum 5 years of pharmacovigilance experience including aggregate safety report writing.

Responsibilities

• Lead and manage PSURs, DSURs, PADERs, and local reports.
• Serve as SME for worldwide aggregate safety requirements.
• Collaborate with Safety, Clinical Development, Medical Affairs, Regulatory.
• Support safety data processing and signal management improvements.
• Assist with responses to safety inquiries from authorities.

Skills

Data interpretation

Cross-functional collab

Clinical judgment

Regulatory & PV knowledge

Organization

Technical proficiency

Education

BSc in life sciences

Advanced degree preferred

Tools

Excel

PowerPoint

Word

Business Objects

Job description

Job Title: PV Drug Safety Consultant
Location: Hybrid – Cambridge, MA 02142
Duration: 09/21/2026 to 09/20/2027 with possible extension
Pay rate: $79.58/hr. on W2

Job Description:

The PV Aggregate Reports Scientist is part of the Safety Surveillance and Aggregate (SSA) Reports team and is responsible for managing the processes for all aggregate reports (PSURs, DSURs, PADERs, and local reports).

In this role, you will:

• Serve as a subject matter expert on worldwide aggregate reporting safety requirements for the PV Scientist team, Safety, and cross-functional partners.
• Respond to safety questions from internal and external stakeholders while reviewing and supporting the authoring of medical and scientific safety information.
• Work closely with vendors, vendor oversight, and Quality Management teams to ensure high-quality standards across PV documents.
• Support process improvement initiatives in collaboration with PV Sciences and cross-functional groups to develop, implement, and maintain compliant, efficient, and consistent global PV processes.

Key Responsibilities:

• Aggregate Report Management: Lead and conduct all aspects of substantive projects, including the authoring and project management of PSURs, DSURs, PADERs, and local reports independently or collaboratively.
• Subject Matter Expertise: Act as an expert on relevant safety requirements, company policies, and aggregate reporting knowledge; represent and articulate processes in cross-Safety and cross-functional forums.
• Schedule & Regulatory Oversight: Support the Aggregate Reports Master Schedule (production, updates, stakeholder reviews), conduct worldwide legislation reviews for aggregate reporting, and provide impact assessments.
• Health Authority Responses: Support authoring responses to safety inquiries from regulatory authorities alongside PV Scientists and key stakeholders.
• Process Optimization: Drive process improvement initiatives to enhance consistency in aggregate reporting, signal management, clinical trial safety oversight, and ad hoc safety responses.
• Implementation: Maintain existing procedures and support the rollout of new PV processes.

Essential Skills and Qualifications:

• Data Interpretation & Communication: Ability to understand, interpret, analyze, and clearly present scientific and medical data verbally and in writing (including medical concepts and terminology).
• Cross-Functional Collaboration: Proven track record of working collaboratively in a team environment across Safety, Clinical Development, Medical Affairs, Clinical Operations, Regulatory, and external colleagues.
• Clinical Judgment: Ability to apply clinical judgment to interpret case information and guide staff on case data evaluation.
• Regulatory & PV Knowledge: Familiarity with pharmacovigilance, drug development, clinical trial safety regulations, and post-marketing safety regulations (including case processing, expedited reporting, and safety databases).
• Organization & Independence: Strong organizational skills with the ability to prioritize tasks independently with minimal supervision.
• Technical Proficiency: Basic knowledge of standard software (Excel, PowerPoint, Word, Business Objects) and familiarity with common safety database systems.

Education & Experience Requirements:

• Education: Bachelor’s degree in biological or natural sciences required; Advanced degree (MSc, PhD, MPH, PharmD, etc.) preferred.
• Experience: Minimum of 5 years of Pharmacovigilance experience, including direct experience in aggregate safety report writing and safety signal management.

About Us:

Founded in 2009, IntelliPro is a global leader in talent acquisition and HR solutions. Our commitment to delivering unparalleled service to clients, fostering employee growth, and building enduring partnerships sets us apart. We continue leading global talent solutions with a dynamic presence in over 160 countries, including the USA, China, Canada, Singapore, Japan, Philippines, UK, India, Netherlands, and the EU. IntelliPro, a global leader connecting individuals with rewarding employment opportunities, is dedicated to understanding your career aspirations. As an Equal Opportunity Employer, IntelliPro values diversity and does not discriminate based on race, color, religion, sex, sexual orientation, gender identity, national origin, age, genetic information, disability, or any other legally protected group status. Moreover, our Inclusivity Commitment emphasizes embracing candidates of all abilities and ensures that our hiring and interview processes accommodate the needs of all applicants. Learn more about our commitment to diversity and inclusivity at https://intelliprogroup.com/.

Compensation:

The pay offered to a successful candidate will be determined by various factors, including education, work experience, location, job responsibilities, certifications, and more. Additionally, IntelliPro provides a comprehensive benefits package, all subject to eligibility.