Associate Jobs in Greenwich, Connecticut | PharmaceuticalCrossing.com
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Associate Jobs in Greenwich






Job info
 
Location
Ridgefield, CT
Posted Date
Aug 11, 17
Info Source
Employer  - Full-Time   

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 ..

 
Location
Ridgefield, CT
Posted Date
Aug 13, 17
Info Source
Employer  - Full-Time   

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, ..

 
Location
Ridgefield, CT
Posted Date
Aug 12, 17
Info Source
Employer  - Full-Time   

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 ..

 
Location
Ridgefield, CT
Posted Date
Aug 17, 17
Info Source
Employer  - Full-Time   

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 ..

 
Location
Ridgefield, CT
Posted Date
Aug 25, 17
Info Source
Employer  - Full-Time   

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 ..

 
Location
Stamford, CT
Posted Date
Sep 18, 17
Info Source
Employer  - Full-Time   

Responsibilities: 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. Monitor ..

 
Location
Hawthorne, NY
Posted Date
Sep 20, 17
Info Source
Employer  - Full-Time  

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 ..

 
Company
Location
Woodcliff Lake, NJ
Posted Date
Sep 20, 17
Info Source
Employer  - Full-Time   

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 ..

 
Company
Location
Woodcliff Lake, NJ
Posted Date
Sep 27, 17
Info Source
Employer  - Full-Time   

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 ..

 
Company
Location
Saddle River, NJ
Posted Date
Sep 30, 17
Info Source
Recruiter  - Full-Time  90  

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 ..

 
Location
Ridgefield, CT
Posted Date
Oct 01, 17
Info Source
Employer  - Full-Time   

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 ..

 
Location
Woodcliff Lake, NJ
Posted Date
Oct 13, 17
Info Source
Recruiter  - Contract     

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 ..

 
Company
Location
Pearl River, NY
Posted Date
Oct 16, 17
Info Source
Recruiter  - Full-Time  

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 ..

 
Location
Melville, NY
Posted Date
Oct 16, 17
Info Source
Employer  - Full-Time   

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 ..

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