Group Communications Specialist
Absa Group
Develop strategic internal content and campaigns for Absa Group, a leading African banking group. Strengthen colleague engagement across digital communication channels.
Open
MSD is a global biopharmaceutical company advancing medicines and vaccines for major health challenges, including cancer, infectious diseases, cardiovascular and metabolic conditions, and prevention-focused care. Known as Merck & Co., Inc. in the United States, Canada, and Puerto Rico, MSD combines scientific research with development and commercial expertise to bring healthcare solutions to people and animals.
Its work spans Human Health, Animal Health, and Research & Development, creating opportunities for professionals across scientific, clinical, commercial, operational, and corporate teams. With activities in regions around the world, MSD’s careers reflect its focus on research, collaboration, inclusion, and responsible progress in global health.
Associate Director, Oncology Regulatory Liaison
Lead regulatory strategy and agency engagement for oncology products at MSD. Support global registrations, lifecycle management, submissions, and compliant product development.
United States
Massachusetts
New Jersey
Pennsylvania$129,000 – $203,100 / year
HybridFull-timeSeniorEnglish RequiredComplianceDescription
- Support oncology products within a regulatory affairs team
- Partner with global regulatory leads on registration and product-maintenance strategies
- Contribute to marketing applications, IND submissions, pediatric plans, and annual or periodic reports
- Track, draft, coordinate, and review responses to regulatory agency requests
- Prepare agency background packages and marketing application documents
- Communicate with regulatory agencies and participate in agency meetings as needed
- Contribute to global regulatory teams and cross-functional meetings
- Evaluate regulatory guidance, precedents, and competitive intelligence
- Help prepare regulatory strategy documents
- Collaborate with Regulatory Operations, Clinical Safety, Labeling, Regulatory CMC, clinical research, and non-clinical safety teams
- Support quality compliance and lifecycle management for oncology programs
- Contribute to label development
- Support regulatory process improvement initiatives
- Handle regulatory administrative activities as needed
Requirements
- Bachelor’s degree and at least 5 years of relevant pharmaceutical industry experience, or a master’s degree and at least 2 years of relevant experience, or an M.D., Ph.D., or related doctorate in biological science, chemistry, or a related discipline with relevant experience
- Experience with drug development
- Previous regulatory experience involving interaction with a major regulatory agency
- Excellent written and verbal communication skills
- Strong organization and the ability to manage varied activities across multiple projects simultaneously
- Flexibility
- Strong scientific and analytical capabilities with close attention to detail
- Oncology product experience is highly preferred
- Eligibility to reside in the United States and Puerto Rico
- Visa sponsorship is not available
- Willingness to travel up to 10%
- A valid driving license is not required
Benefits
- Annual bonus
- Long-term incentive, where applicable
- Medical, dental, and vision coverage
- Additional insurance benefits for employees and families
- Retirement benefits, including a 401(k) plan
- Paid holidays
- Vacation leave
- Compassionate leave
- Sick leave
- Hybrid work arrangement
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