- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Specialist will work as part of a global regulatory pharmaceuticals team to create and maintain global registration dossiers in the Veeva ... Specialist 's responsibilities will include:Creating global and country specific regulatory dossiers in the Veeva Submissions Platform.Assisting with the… more
- Stryker (Mahwah, NJ)
- …We are currently seeking a **Senior Regulatory Affairs Specialist ** ... and interact with regulatory agencies and notified bodies. The Senior Regulatory Affairs Specialist is the Regulatory SME on cross-functional teams… more
- Merck (Rahway, NJ)
- **Job Description** The Specialist will work as part of a global regulatory pharmaceuticals team to create and maintain global registration dossiers in the Veeva ... Submissions platform. The Specialist 's responsibilities will include: + Creating global and country...responsibilities will include: + Creating global and country specific regulatory dossiers in the Veeva Submissions Platform. + Assisting… more
- AbbVie (Florham Park, NJ)
- …level will be determined by the qualifications listed below. Purpose Provides specialist medical and scientific strategic and operational input into core medical ... affairs activities such as: healthcare professional/provider interactions (HCPs, Patients...into and influences the development of asset strategy. Provides specialist medical insights, and executes on data generation, communication,… more
- BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
- …decisions and guide product strategy -- Including cross-functional collaboration with R&D, Medical Affairs , Market Access, Regulatory Affairs and Marketing + ... **Job Description Summary** The HEOR Manager/ Specialist - MDS is accountable for ensuring execution of...BD while informing the broader scientific strategy with Medical Affairs . **Job Description** We are **the makers of possible**… more
- ManpowerGroup (Wayne, NJ)
- …of three years of experience with medical devices or pharmaceuticals in a Quality, Regulatory Affairs , or Regulatory Compliance role. + Working knowledge of ... Our client, a leader in the medical device industry, is seeking a Quality Compliance Specialist to join their team. As a Quality Compliance Specialist , you will… more
- Hackensack Meridian Health (Hackensack, NJ)
- …+ Minimum of 2 years experience in a Senior Clinical Data Coordinator or Senior Regulatory Specialist role, or at least 4 years related experience in the field ... compliant study conduct according to all relevant local, federal, and state regulatory and institutional Polices and Standard Operating Procedures. This role carries… more
- Hackensack Meridian Health (Hackensack, NJ)
- …+ Minimum of 2 years experience in a Senior Clinical Data Coordinator or Senior Regulatory Specialist role, or at least 4 years related experience in the field ... compliant study conduct according to all relevant local, federal, and state regulatory and institutional Polices and Standard Operating Procedures. This role carries… more
- Sanofi Group (Morristown, NJ)
- …the clinical data. + Interact with relevant teams Innovation, Regulatory , Pharmacovigilance, Evidence generation (eg biostatisticians, Medical Writers, Monitoring ... team, eDS, etc.), Scientific Affairs and Growth (eg Marketing representatives when relevant). Common...part of the CTD; Ensure the eDS (electronic Document Specialist ) is involved in the project at an early… more
