Biotech Project Manager Jobs

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A leading global Biotech organization is currently recruiting for a Project Manager based in Cambridge, MA. This is a long term 6 month contract, paying a competitive hourly rate dependant on experience and qualifications. This position is interviewing immediately and can start as soon as possible (notice period is also fine). The Project Manager, reporting to the Associate Director of Safety and...
Contract Sr. Clinical Project Manager The Sr Project Manager provides project management support and leadership to the E2E SC workstreams, sub-workstreams and teams, and is accountable to the PMO lead his/her workstream lead/s. The Sr Project Manager must apply project management best practices in the development, initiation, planning, execution, control and closing of workstream projects, accord...
JOB SUMMARY: A Clinical Project Manager (CPM) is responsible for the execution of a clinical trial or suite of clinical trials from protocol design to the final clinical study report. They manage the process and people involved though matrix reporting. The position is responsible for coordinating all efforts for the trial both within the Company and through a wide variety of vendors. A CPM coordi...
AAIPharma Services is a leading provider of drug development and manufacturing services to pharmaceutical, biotech and medical device companies around the world. With over thirty years of drug development expertise, we offer exciting and challenging career opportunities in a dynamic and growth oriented-business. Headquartered in coastal Wilmington, NC and just minutes from beautiful Wrightsville ...
Sr. Project Manager 1 year contract Pay: 75.00/hr. Key Responsibilities: The Sr Project Manager provides project management support and leadership to the E2E SC workstreams, sub-workstreams and teams, and is accountable to the PMO lead his/her workstream lead/s. The Sr Project Manager must apply project management best practices in the development, initiation, planning, execution, control and ...
Title: Project Manager Job ID: 908 Industry: Biotech/Pharmaceutical Division: Worldwide Operations Location: Thousand Oaks, CA Duration: 6 Month Contract Pay Rate Range: Depends on Experience (W-2 all inclusive rate) Job Details: The Sr Project Manager provides project management support and leadership to the E2E SC workstreams, sub-workstreams and teams, and is accountable to the PMO lead...
Streffco Consultants, Inc., is an international staffing and systems integration organization. We provide technology and business operations resources on a project, contract, contract-to-hire or direct hire basis. Title: Project Manager – Drug Safety Job ID: 5687 Industry: Biotech/Pharmaceutical Location: Cambridge, MA Duration: 6 Month Contract Pay Rate Range: Depends on Experience (W-2 all...
The Clinical Project Assistant will be a member of the Jazz Pharmaceuticals Clinical Operations team. The Clinical Project Assistant’s responsibilities include (but are not limited to) the following: General administrative support to the Clinical Project Teams Assist project teams with study specific tasks Ensure trial master files are current and maintained Co-ordination of Investigator paym...
Our client of 8 years, is a Pharmaceutical Company recognized globally for their unparalleled development and manufacturing services for the world’s leading pharmaceutical, biotechnology, and healthcare companies. With four cGMP facilities and over a million square feet of state-of–the-art manufacturing, packaging, and distribution space, our client offers full service outsourcing solutions inclu...
GLOBAL CLINICAL PROTOCOL MANAGER - LATE PHASE SPONSORED RESEARCH WITH ONCOLOGY REQUIREMENT #14-00927 RECRUITER: CINDI PISNOY JOB LOCATION: PLAINSBORO, NJ SEPTEMBER 2, 2014 Expected Areas of Competence: General · Manages successful execution and completion of assigned global clinical Phase IIIb/IV publication/medical informing trials within CSR&O Late Phase Sponsored Research unit, in adhere...
Job description: Lab Manager, bioanalytical method development Location: Middleton, Wisconsin Description PPD is a leading global contract research organization providing discovery, development and post-approval services as well as compound partnering programs. With offices in 46 countries and more than 13,000 professionals worldwide, PPD applies innovative technologies, therapeutic expertise a...
The basic purpose is to ensure efficient and effective management of PPD resources. The objective is to supervise and assist group leaders and scientists in laboratory operations with tasks such as scheduling, resource management, technical and compliance related issues. To plan, direct and implement improvements in systems, processes and procedures to increase efficiency, productivity and quality...
Xcenda is a premier, full-service consultancy and leading managed markets agency. For more than 2 decades, global biopharmaceutical companies as well as emerging pre-commercialization phase firms have turned to Xcenda for strategic insights, health economics and outcomes research expertise, and reimbursement support. We help manufacturers successfully commercialize innovative medical treatments an...
Title: Manager, Clinical Data Management Job ID: 780 Industry: Biotech/Pharmaceutical Location: Thousand Oaks, CA Duration: 12 Month Contract Pay Rate Range: Depends on Experience (W-2 all inclusive rate) Job Details: Management responsibility for Clinical Data Management (CDM) activities related to study initiation, including the development of paper case report forms (CRFs), electronic CR...
any combination will do, must have pharma experience ASSOC BIOSTATISTICIAN/ BIOSTATISTICIAN - MANUFACTURING up to 97k base Benefits - Full Relocation Assistance Available - Possible for the ideal candidate Bonus Eligible - Yes Interview Travel Reimbursed - Yes The Assoc.Biostatistician/Biostatistician (MANUFACTURING) will serve as the Statistician for the Biologics Facility(s) and is respons...
About Xcenda Xcenda, a business unit of AmerisourceBergen Corporation, is an integrated, world-class health care consulting organization focused on value, reimbursement and patient access. For more than 2 decades, Xcenda has helped global biopharmaceutical companies as well as emerging early-phase firms successfully commercialize innovative medical treatments and technologies in complex and ...
EMD Serono is the biopharmaceutical division of Merck KGaA, Darmstadt, Germany, a global pharmaceutical and chemical group. We strive to create value and benefit patients by transforming medical science into breakthrough solutions in our core therapeutic areas of neurodegenerative diseases, fertility and metabolic endocrinology, as well as oncology and autoimmune/inflammatory diseases as emerging ...
Any combination will do Director GRA Combination Products- Medical Devices ASSOC DIR BIOSURGERY REGULATORY AFFAIRS, * medical device Director, Global Regulatory Affairs Combination Products- Medical Devices Director Global Regulatory Affairs Combination Products and Medical Devices Senior Manager, Global Regulatory Affairs - Medical Devices Joe, 860 889 4141, until 9 pm Eastern, 7 days a wee...
TypeRegular Full-Time Job Code*LI-JL2 Overview: Mallinckrodt Pharmaceuticals is pleased to bring Questcor and its entire business into our company. The former Questcor organization will be known as the Autoimmune and Rare Diseases business within Mallinckrodt’s Specialty Pharmaceuticals segment. We will continue their focus on the treatment of patients with serious, difficult-to-treat autoimmu...
Job Number: 422667 Global Studies Assocaiate 4016556 Skills: 2 yrs Industry exp CTA (Clinical Trial Associate) Exp CRC (Clinical Research Coordinator) Exp Clinical Project Assistant or Associate Exp Regulatory Exp CTMS (Clinical Trial Management System) Exp Global Exp GCP/ICH Exp Required Experience: Have at least 2 years of previous clinical research experience. In order of significance, mos...

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