Associate Director, Global Medical Affairs – Program Oversight

Joulé
Raritan, NJ, United States
Full-time

Title : Associate Director, Global Medical Affairs Program Oversight Location : Must be local NJ and go onsite as needed Type : Embedded Start Date : ASAP Leading Pharmaceutical Company located in NJ is hiring a Associate Director, Global Medical Affairs Program Oversight w / 5+ years industry experience.

If you want to be a part of this groundbreaking work, please apply! The Associate Director, GMAF Program Oversight will be responsible for coordinating efforts and project management activities.

Currently, an education tool is being created to launch a program that after a baseline test, will direct internal employees on to specific learning materials.

Scientific Training activities might span across therapeutic areas, including Oncology, Immunology, Neuroscience and Pulmonary Hypertension assets, so the ideal candidate will be required to work in a fast-paced cross functional setting with an adaptable mindset. Key Responsibilities :

  • Support the building and launch of education tools to cover applicable internal products and competitor information
  • Liaise between vendor and internal stakeholders to provide status updates (includes communication sent to leadership teams), timelines and project management
  • Help with meetings set-up, agendas and meeting minutes to keep track of action items
  • Oversee program metrics and reporting
  • Review feedback survey responses and keep track of approved enhancements implementation
  • Own the Support mailbox oversight and follow up on issues resolution Qualifications :
  • Minimum of a Bachelor’s Degree in any related field ideally scientific / medical background or Business Administration with experience in Pharma projects
  • MBA, Masters or other higher education degrees desired but not mandatory
  • Project and program management experience required
  • Proven experience working in an organized and systematic environment
  • Pro-active, fast learner, detail oriented
  • Excellent communication skills
  • Minimum of 5-8 years of relevant work experience
  • 4 hours ago
Related jobs
Promoted
Daiichi Sankyo
Bernards, New Jersey

As a member of Global Medical Affairs Team (GMAT, or Joint Medical Affairs Team for Alliance compounds) and as a subject matter expert (SME), in alignment with the GMAT Lead, develop an Integrated Evidence Plan (IEP), which includes an evidence gap assessment, gap prioritization and strategic delive...

Promoted
Sun Pharmaceutical Industries, Inc.
Princeton, New Jersey

Employees are eligible to participate in Company employee benefit programs which include medical, dental and vision coverage; life insurance; disability insurance; 401(k) savings plan; flexible spending accounts; and the employee assistance program. We are proud that our global workforce is bound by...

Promoted
Sun Pharmaceutical Industries, Inc.
Montgomery, New Jersey

Employees are eligible to participate in Company employee benefit programs which include medical, dental and vision coverage; life insurance; disability insurance; 401(k) savings plan; flexible spending accounts; and the employee assistance program. We are proud that our global workforce is bound by...

Promoted
Daiichi Sankyo
Bernards, New Jersey

Daiichi Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and technology. In addition to a strong portfolio of medicines for ca...

Promoted
Novo Nordisk
Plainsboro Township, New Jersey

Lead the Global Regulatory Matrixed Team in defining and executing the global regulatory strategy for assigned programs to ensure timely and high-quality regulatory deliverables to the GPTs. You will report to the Senior Director - Global Regulatory Portfolio Lead. Serve as a member of the Global Pr...

Joulé
Raritan, New Jersey

Title: Director, Global Medical Affairs, Internal Education. Leading Pharmaceutical Company located in NJ is hiring a Director, Global Medical Affairs, Internal Education w/ 5+ years industry experience. Support the curation, checks and update process for previous training materials created by agenc...

Genmab
Princeton, New Jersey

The Team Lead for Authoring Support Group will be part of the Global Regulatory Operations group and will develop and manage the authoring support group within Regulatory Affairs (RA) to ensure timely and high-quality document delivery to the Regulatory Publishing Group. You will oversee the impleme...

Katalyst HealthCares & Life Sciences
NJ

Serves as primary contact for cross-functional Labeling Team Member (CFLT), eg Global Regulatory Team Lead (GRTL), Medical Surveillance Team Lead (MSTL), Functional SMEs, Documentation Leads and Medical Writer, Dossier Lead and Submission Manager, also serves as interface for Country Regulatory Mana...

Acadia Pharmaceuticals Inc.
Princeton, New Jersey

The Senior Medical Director will lead the development and execution of the medical strategy for Rett Syndrome. Primary Responsibilities</u></strong></p><ul><li>Provide scientific and medical leadership, including development of strategic plans, identifying specific unme...

Bristol Myers Squibb
US,NJ,Giralda,Madison

Establishing a clear, viable and compelling strategy for the Medical Communications, aligned with overall Medical vision, strategy and objectives, and ensure delivery of timely and high-quality medical publications, scientific content, medical education, medical information, and congress presentatio...