Medical affairs jobs in Clifton, New Jersey (NJ) State

AlliedTravelCareers is working with MedPro Healthcare Staffing to find a qualified OT in Clifton, New Jersey, 07011! Pay Information $1,733 per week About The Position MedPro Healthcare Staffing , a Joint Commission-certified staffing agency, is seeking a quality Occupational Therapist for an ass...

This role primarily focuses on late-stage pipeline and marketed products, interfaces with cross-functional teams including US medical affairs, marketing, market access global value and access teams, commercial to align strategies in customer research activities and development of external communi...

Join our client's team as a Medical Director, Medical Affairs, where you will provide medical, scientific, strategic, and operational leadership. Job Title: Medical Director, Medical Affairs. Initiate and lead medical affairs activities, data generation, and dissemination to support the overall m...

This role primarily focuses on late-stage pipeline and marketed products, interfaces with cross-functional teams including US medical affairs, marketing, market access global value and access teams, commercial to align strategies in customer research activities and development of external communi...

The assignment involves receiving and reprocessing Reusable Medical Equipment which will be used by various customers within the medical center for scheduled or emergency procedures. Working knowledge of medical terminology, anatomy and physiology, microbiology, medical conditions and procedures....

The Medical Director (Medical Affairs) will report into the Medical Affairs Department and is responsible for clinical support and consultative activities across the PBM. The Medical Director (Medical Affairs) will report into the Medical Affairs Department and is responsible for clinical support...

Responsible for the creation and development of scientific and medical content for use by US Medical Affairs and Field Medical external activities and training. Are you ready to build your career by joining a global pharmaceutical company? If so, our client is hiring a Medical Affairs Content Dev...

US medical affairs, HEOR, marketing, market access, global value and access teams, commercial) to prioritize projects toward achieving effective utilization of resources. The base salary range for the Director, Real World Evidence, Global Medical Affairs is from :213,500-280,200Under current guid...

The Associate Scientific Director will provide scientific/medical leadership and support to the execution and implementation of USMA strategies for the Multiple Myeloma Cell Therapy franchise by representation in cross-functional teams, and collaboration within global medical affairs. Excellent a...

The Medical Director, US Medical Affairs provides medical leadership for medical affairs strategy, planning and supportive tactics for assigned therapeutic area. This role is responsible for working with key stakeholders to develop and execute the medical affairs plan, including post-marketing re...

The Medical Director (Medical Affairs) will report into the Medical Affairs Department and is responsible for clinical support and consultative activities across the PBM. The Medical Director (Medical Affairs) will report into the Medical Affairs Department and is responsible for clinical support...

In partnership with cross functional global medical affairs, they will support the design and implementation of the US integrated medical plan. Excellent analytical skills and solid experience in translating medical/clinical information into medical affairs strategies, with a robust understanding...

This opportunity entails being responsible for managing assigned project(s) throughout their full lifecycle including developing the scope and technical sections of proposal and procurement documents to participating in contract negotiations and overseeing the delivery of the project plan to succ...

The CUSO/IHC Local Regulatory Reporting Department is seeking a Vice President to assist in the implementation of the required regulatory reports submitted to the Federal Reserve Bank, and other regulators. Responsibilities: ·         Assist in maintaining and enhancing the BAU production process...

Two years of proven experience in scientific or medical affairs at a biotech or pharmaceutical companyAt least two years in a Medical Science Liaison roleThree or more years of clinical practice, clinical research, or medical research. Medical Science Liaison, IgG4 - Rare DiseaseLiveWhat you will...

Regulatory Affairs SpecialistPosition This hire will be a member of the Firm’s Regulatory group which is responsible for exam oversight, branch inspections, regulatory change tracking, governance related tasks and additional ad-hoc tasks. The Firm’s Regulatory Group is housed within its Legal Dep...

Data entry clerks come from all different backgrounds including, data entry, telemarketing, customer service, sales, clerical, secretary, administrative assistant, warehouse, inventory, receptionist, call center, part-time, retail fields & more. ...

Graduate from an accredited Medical Assistant/Medical Technologist school/program and holds a valid Certificate of Completion. Obstetrics/Gynecology (OB/GYN) Certified Medical Assistant (CMA) in Englewood, NJ. Perform Medical Assistant duties in accordance with the current Joint Commission’s Nati...

We are seeking a talented Technical Writer to join our team at a leading financial institution. As a Technical Writer specializing in IT Network Documentation, you will be responsible for creating clear, concise, and accurate documentation for our network infrastructure and related systems. Prove...

Microsoft PowerPoint , Excel, Word, SharePoint, Microsoft Project, and Microsoft Visio is a MUST. ...

The Senior Project Manager role is to plan, execute and finalize projects with high quality deliverables according to deadlines and within budget. What are we looking for in our Senior Project Manager?. Plan, schedule and maintain project milestones using appropriate tools and project team meetin...

Global Regulatory Affairs Operation（Sr. This position belongs to Global regulatory affairs department, serving the global Market which encompasses China US, EU, AUS and others. This role requires a detail-oriented professional who can oversee all regulatory affairs and quality assurance activitie...

Looking for a new challenge as a Heavy Civil Construction Project Manager? Look no further! We are currently working with a client that is seeking a highly experienced Project Manager with expertise in sewer, piping, drainage and road construction. Managing project teams and delegating tasks to e...

The Director of Policy and Regulatory Affairs will be responsible for managing Elevate’s relationships and policy positions at PJM, federal and state regulatory agencies, and state legislative bodies. Director of Policy and Regulatory Affairs – PJM Region. The position reports to the Vice Preside...