Job Information
System One Global Medical Affairs Project Manager in Raritan, New Jersey
Title: Global Medical Affairs Project Manager
Location: Must be local Raritan, NJ and required to go onsite 2 days a week onsite
Type: Embedded
Start Date: ASAP
Leading Pharmaceutical Company located in NJ is hiring a Global Medical Affairs Project Manager 3+ years industry experience. If you want to be a part of this groundbreaking work, please apply!
Responsibilities:
Advisory Board/Publication meeting logistics and management
Advisory Boards – CWT sourcing request, manage contract, PO, SOW, Totality
Track and manage advisor contract redlines and communicate with contracting team
Totality submissions (20 – 50/year) for all medical affairs projects including pub support, medical advisory boards, sponsorships for Oncology. Ensuring all medical affairs are compliant and get all appropriate compliance reviews with Health Care Compliance Officer
Congress planning and medical education – coordinate activities with vendor agencies, GMA personnel, and all internal company stakeholders
SharePoint Management
Manage email distributions
Contract execution of projects – eMP request for contract redlines, new templates. Request for PO increases, Work Order amendments. Work with contracting team to follow/track contracts from Totality approval to contract execution, troubleshooting and communicating along the way
Maintain trackers, finance/budget tracking for Oncology. Maintain overall contract tracking and cross reference of eMP, Totality, contract, and PO numbers. Follow up on outstanding contract requests and tracking throughout the process.
Weekly/bi-weekly meetings with portfolio and disease area teams
Requirements:
Bachelor’s degree in Life Sciences, Business Administration, Project Management, or a related field
5+ years of project management experience, preferably in the pharmaceutical or healthcare industry
Proven experience managing advisory boards or similar initiatives
Strong project management skills with the ability to manage multiple projects simultaneously
Familiarity with regulatory requirements
Excellent communication and interpersonal skills, with the ability to engage with KOLs and senior stakeholders
High attention to detail and strong organizational skills
Experience with Microsoft Office products
Strong problem-solving abilities and proactive approach to challenges
This role may require additional travel for on-site congresses and advisory board meetings
Ability to work in a fast-paced, dynamic environment with tight deadlines
System One, and its subsidiaries including Joulé, ALTA IT Services, CM Access, TPGS, and MOUNTAIN, LTD., are leaders in delivering workforce solutions and integrated services across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible full-time employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.
System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.
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