Trabajos pharmacovigilance scientist en Clifton, New Jersey (NJ) State

Talent4Health is seeking a travel Pharmacist for a travel job in edison, New Jersey. Required Certifications & Licensure:-3725 Certified Pharmacist – Must have taken and passed their board certification exam and received the appropriate certificate indicating attainment of board certification. Re...

Posted job title: Pharmacist (Clinical) Pharmacy: Pharmacist (Clinical). MedPro Healthcare Allied Staffing is seeking a travel Pharmacist for a travel job in Edison, New Jersey. Joint Commission-certified staffing agency, is seeking a quality Pharmacist for a contract with one of our top healthca...

Responsibilities include backing up networks and laptops of employees who are no longer with the company, retaining both unstructured data (emails, etc) and structured data (systems data, formal documentation, etc), producing this data on demand for the legal department and running QC on the data...

Job Title: Operations Project Manager Hybrid role in Jersey City NJ Duration: 12 Months Business Overview: ...

As the Associate Director, US Pharmacovigilance, you will be responsible for overall compliance of tasks within applicable regulations, SOPs, and guidelines, provide Pharmacovigilance expertise and oversight to Ferring staff and serve as PV Representative for assigned Ferring projects. Serve as D...

The key areas of focus include: (1) diversity in clinical trials, (2) clinical trial recruitment and (3) general education and awareness of clinical trials. The Associate Director, Clinical Trials Communications role within our Research & Development organization, will support our strategic enter...

Talent4Health is seeking a travel Pharmacist for a travel job in Edison, New Jersey. Valid New Jersey Pharmacist License , BLS - AHA. ...

Research Associate/Senior Research Associate. We are looking for a Research Associate/Senior Research Associate to join our team. Y-mAbs seeks a Research Associate/Senior Research Associate to support our cell-based assay capabilities to screen, characterize, and evaluate drug candidates. ...

Senior Construction Project Manager. Prepare project schedules and budgets, including General conditions and cash flow projections. Work closely with Project Accountant assigned to project, fully comply with ACR process. Oversee and mentor Assistant Project Managers and Administrative staff. ...

The Data Analyst will be responsible for specialty pharmacy data operations. The role will lead logistics related to SP data RFPs, contracting, and CPC reviews and will drive the day-to-day operations and integration of specialty pharmacy data in downstream processes, including the Patient E2E ec...

Growing family owned company is recruiting for a Food Safety Specialist. You will lead the maintenance of current food safety and quality system, coordinate tasks among departments to identify, solve and prevent problems affecting product quality, maximize productivity, and comply with customer a...

We are searching for a (Senior) Translational Data Scientist. You will work on the following data types; clinical response, tumor transcriptomic/genetic data as well as imaging and circulating biomarkers to support various drug candidates. Utilising various cutting-edge data science tools; AI, ML...

As a Warehouse Management Project Manager, you will play a pivotal role in overseeing and implementing warehouse management projects within our organization. Warehouse Management Project Manager. Your responsibilities will include managing project timelines, budgets, resources, and ensuring the s...

Job Title: Clinical Trial (RRG) Eligibility Liaison. Proficient knowledge of GCP/ICH, drug development process and clinical trial operations. Functional Area Description: The RRG Eligibility Liaison (REL) employs scientific and technical expertise to track, coordinate and enforce the timely deliv...

Vice President/P&C Actuary/Data Scientist opening in New Jersey. Lead team of 7 actuaries and data scientists/predictive modelers for all Personal and Commercial lines of business; develop analytics strategy to deliver enhanced efficiencies and outcomes; partner with IT, Underwriting, Operations,...

The Clinical SOP Writer edits and performs QC review of clinical procedures. The Writer may also eventually work with Process Owners, Subject Matter Experts (SMEs), and relevant stakeholders to develop new and revise existing clinical procedures. The Writer ensures procedures and associated forms...

Candidate should have deep understanding of Project management. Defining the Project Management Methodology. Candidate should have deep understanding of project metrics and reporting. ...

IPG Health Medical Communications is home to the world’s most celebrated and awarded Med Comms agencies. We are 800 experts obsessed with combining science, creativity and technology to create exceptional medical communications solutions for our clients. The VP, Account Director is responsible fo...

Project Engineer or Project Manager (highly preferred). Interface with multiple departments to develop project requirements and stakeholder needs. Implement necessary changes to the project scope of work, deliverables, timelines, and resources through the construction phases. Develop requests for...

We're Hiring: Project Manager**. Project Manager to join our team in Montvale NJ. This is an in-person role perfect for someone with a strong background in project management, brimming with energy, and a clear understanding of our company's vision. Proven experience in project management within t...

THE ARMY HEALTH CARE ADVANTAGE.As a member of the Army health care team, you’ll receive benefits that you won’t be able to get in a civilian career.Feel inspired with great case diversity and over 40,000 visits coming into the U.Army medical facilities and clinics around the world every day.See a...

Senior Medical Director, Clinical Development. This position will be be responsible for providing medical oversight for assigned programs and will be focused within my client's Immunology portfolio. You will serve as the study director for assigned programs, driving design and execution from prot...

Under minimal supervision, the Medical Writer will critically evaluate, analyze, and interpret the medical literature to select primary resource materials for adequate study design, statistical significance, scientific rigor and absence of bias. Mentor medical writers and other members of the pro...

Under minimal supervision, the Medical Writer will critically evaluate, analyze, and interpret the medical literature to select primary resource materials for adequate study design, statistical significance, scientific rigor and absence of bias. Mentor medical writers and other members of the pro...