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Associate Director, Clinical Trial Programming','179105','!*!Description:
Directs the activities of a group of
programmers with the goal of providing programming expertise to support
international drug development, international registrations, local marketing
and the ..
Clinical Compliance Lead (Senior Associate Director) 2 Openings)','176821','!*!Boehringer Ingelheim is currently hiring two (2) Clinical Compliance Leads to join the Quality Management Team.Description:
The Clinical Compliance Lead is a lead role, ..
Senior Associate Director, Pharmacometrician OR Principal Pharmacometrician','174040','!*!Senior Associate Director Description:
The Sr. AD will independently perform high quality pharmacometric (PMx) analyses on a project and study level essential for internal decision ..
Associate Director/Manager, DRA Product Group','172760','!*!Description:
Provide US regulatory input to project teams supporting early, middle and late-stage drug development.
To lead and manage the compilation and submission of possibly complex US ..
Senior Associate Director, Payor Solutions','179908','!*!Description: Develop and plan push/pull-through effort in assigned Payor Accounts and Payor Sales Regions. Co-Lead execution of account-specific push/pull-through plan in collaboration Payor sales Account Executive. Maintain ..
Book-in and perform case processing of serious ICSRs and other qualified case reports in the safety database.
Manage and track receipt of initial and follow-up reports from study sites.
Compile, review and evaluate acceptability for filing of ANDA?s, ANDA Supplements and ANDA Annual Reports, as well as assembly of abbreviated new drug applications.
Assist in the processing of annual facility ..
Assist Director to translate and provide recommendations for all brands the impact of public sector trends and initiatives with respect to patient access, reimbursement, and customer satisfaction, and translate into meaningful ..
Associate Director, Biostatistics sought by pharmaceutical and healthcare company in Woodcliff Lake, NJ. Serve as the lead biostatistician for clinical studies and projects, accountable for all statistics-related activities throughout drug development ..
Job TitleAssociate Director Commercial Regulatory Affairs Division/DepartmentGlobal Regulatory Affairs Job SummaryProvide commercial regulatory .strategic input into the review and approval of effective yet FDA compliant commercial (advertising and promotion) campaigns, pre-commercialization ..
Associate Director, Human Resources - Medicine & Regulatory Affairs','1711016','!*!Description:
The Associate Director, Human Resources is a member of the HR Business Partner (HRBP) team dedicated to supporting BI's Medicine & Regulatory ..
nPharmaceutical Company HiringTitle: Regulatory Affairs Associate (PART-TIME) Location: Woodcliff Lake, NJ W-2 Contract (12 Month Duration) PART-TIME (3 Days Per Week) The candidate should have 3-5 years experience independently compiling routine ..
Pearl River, NY
What you'll be doing
Designs clinical studies to meet the stated objectives. Directs clinical scientist (CS) in writing the synopsis and protocols. Approves protocols and amendments. Provides medical ..
The QC Analyst- Senior Associate is responsible for complying with the company’s Quality Control efforts. This includes the performance of area responsibilities necessary to ensure that Laboratory activities are performed in ..