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Excellent Job Opportunity for the position of Expert Clinical Manager II (*******) Ref No.: 16-19482 Location: East Hanover, New Jersey Position Type: Contract Start Date / End Date: 03/13/2017 to..
The Manager, Clinical Quality Assessment (CQA) Auditor is responsible for the initiation, conduct, and follow-up of audits as assigned by CQA Management. Within the frame of the Manager, CQA Auditoru2019s..
u003Cbu003ERequisition ID: u003C/bu003EREG004020u003Cbr/u003Eu003Cbr/u003Eu003CP style=MARGIN-BOTTOM: 0px; MARGIN-TOP: 0px\u003Eu003CFONT face=Arialu003Eu003CFONT size=2u003EMerck u0026amp; Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader..
Must Haves: nB.S. or M.S. in chemistry, pharmacy, biology or a related pharmaceutical science n5 years QA experience from GMP pharmaceutical/biopharma or other n5 regulated industry nExp w/batch record and..
Pharmaceutical Packaging Engineer in New Brunswick New Jersey Pharmaceutical Packaging EngineerNew Brunswick, NJ Apply with System One Type:Contract Category:Scientific & Clinical Job ID:133623 Date Posted:10/11/2018 We are looking for a..
Sr. Data Manager in Berkeley Heights New Jersey Sr. Data ManagerBerkeley Heights, NJ Apply with System One Type:Contract Category:Scientific & Clinical Job ID:133725 Date Posted:10/11/2018 Sr. Data Manager Responsibilities: Oversee..
Position Description Lead the technical design and implementation of new digital capabilities supporting the R&D Strategy & Planning and Global Clinical Operations functions. Effectively work on large complex programs in..
Business Services Associate (Executive Assistant) in PRINCETON New Jersey Overview Our people make the difference. We believe in our employees and give them daily opportunities to grow as professionals and..
Sr. Data Manager nResponsibilities: n n Oversee the management of clinical trial databases from study start up to study closure. n Be able to review and understand protocol synopsis and..
ESSENTIAL DUTIES AND RESPONSIBILITIES To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. Ensure compliance with ICH – GCP guidelines and all pertinent..
Other Locations: US- NJ- Summit East Description Celgene is a global biopharmaceutical company leading the way in medical innovation to help patients live longer, better lives. Our purpose as a..
Mallinckrodt Pharmaceuticals, a leader in specialty pharma with a focus on Auto-Immune, Rare Disease, Acute/Critical Care and Regenerative Medicine, is recruiting a Clinical Trial / Senior Clinical Trial Manager. This..
u003Cbu003ERequisition ID: u003C/bu003EREG003950u003Cbr/u003Eu003Cbr/u003Eu003Cp style=MARGIN-BOTTOM: 0px; MARGIN-TOP: 0px\u003Eu003Cfont face=Arial size=2\u003EMerck u0026amp; Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader..
Typical Daily Work schedule (start/end times) = 830am-5pm (some flexibility in start/end times as long as full day is worked) 40 Hrs/Week Weekend work not required, but might be needed..
Job Summary Meet Recruitment is currently engaged with a Global BioPharma in Bridgewater, New Jersey who is seeking a Sr Medical Affairs Director with a background in Rare Diseases. Job..
u00a0Clinical Study Director The Clinical Study Director (CSD) will provide appropriate medical input & support for all activities related to clinical studies such as medical training, feasibility, medical review of..
Job Description 927 million. Thatu2019s how many lives our products touched in 2017. And while weu2019re proud of that fact, in this world of digital and technological transformation, we must..
Role Purpose GCS Clinical Trial Supply Manager (CTSM) defines and executes an optimal clinical trial supply strategy for a clinical trial including effective risk management to ensure supply continuity to..
Corporate Counsel, Business Development & Global Alliances Celgene • Summit NJ Job #751661267 Description Celgene is a global biopharmaceutical company leading the way in medical innovation to help patients live..
Digital Capability Management, Solution Architecture & Delivery, Clinical Operations in Hopewell New Jersey Position Description Lead the technical design and implementation of new digital capabilities supporting the R&D Strategy &..
QA Specialist - Pharmaceutical Packaging and Labeling in New Brunswick New Jersey QA Specialist - Pharmaceutical Packaging and LabelingNew Brunswick, New Jersey Apply with System One Type:Contract Category:Scientific & Clinical..
Manager/Senior Manager Healthcare Law Compliance Monitoring in Princeton New Jersey Employee will be responsible for consistently delivering outcomes with cross functional impact. Employee will be expected to leads and/or significantly..