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Job matches 217

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Senior Clinical Research Associate - Remote

Company: SynteractHCR Deutschland GmbH
Location: Kansas City, MO
Salary: On Application
Benefits: Excellent
Closing Date: 20 Feb 17More Details
Overview The Senior Clinical Research Associate is responsible for performing monitoring and tracking study progress, thereby contributing to the overall management of clinical trials in accordance with the standards ICH-GCP and applicable local regulations and Standard Operating Procedures (SOPs).  The job may include clinical lead activities as well as the mentoring and training of less senior CRAs.

Contract CTM

Company: EPM Scientific
Location: San Francisco
Salary: Negotiable
Closing Date: 04 Mar 17More Details
Contract Clinical Trial Manager- San Francisco Bay Area – 6 month contract with high possibility of extension  2 Clinical Trial manager positions are available for...

Director of Epidemiology – Connecticut- Global Pharma

Company: Meet
Salary: Competitive
Closing Date: 17 Mar 17More Details
This person is an expert in epidemiology and Health Outcomes at a Director level within pharmaceuticals.

This global pharmaceutical company is rapidly growing the team and growing the strategic area of the business.

Senior Consultant - Global Life Sciences

Company: Morgan Prestwich Pharmaceutical Recruitment
Location: Various
Salary: Competitive
Benefits: Standard Benefits Package
Closing Date: 17 Mar 17More Details
Our Client is a leading global strategy consulting firm focusing on issues for a variety of biopharmaceutical companies, pharmaceutical companies, medical device companies, and government health authorities. Pricing and Market Access, Value Demonstration, Portfolio Optimisation, Commercial Planning, and Government Policy Advisory.

Contact Clinical Study Manager, Home Based in North Carolina

Company: Barrington James Clinical
Salary: Competitive
Closing Date: 17 Mar 17More Details
An incredible Home Based contract opportunity working with a niche but global sponsor in North Carolina

Sr. Manager, Statistical Programming- New Jersey

Company: RBW Consulting
Salary: Competitive
Closing Date: 17 Mar 17More Details
Support data standardization, implement submission data standards, maintain and govern clinical data standards, industry standards and CSO business strategy, provide support to teams working across multiple disciplinaries to ensure high quality and timely eSub deliverables.

Associate Director - Statistical Programming, NJ

Company: RBW Consulting
Salary: Competitive
Closing Date: 17 Mar 17More Details
This position manages programmers responsible for statistical programming activities for multiple late stage (phase II - IV) drug/vaccine clinical development projects, in one or multiple therapeutic areas with a strong focus on oncology.

Senior Principal Statistical Programmer ~ Pharma

Company: RBW Consulting
Location: Cambridge, MA
Salary: On Application
Benefits: $On application –strong bonus and supporting package
Closing Date: 17 Mar 17More Details
An international Pharmaceutical company with a superb industry reputation looks to bolster its Statistical Programming group.

Senior Medical Director - Medical Communications

Company: EPM Scientific
Location: New York
Salary: 100,000+
Benefits: Bonus + Industry Leading Benefits (Healthcare, 401k, Disability)
Closing Date: 03 Mar 17More Details
Forward Thinking Medical Communication agency seeking full-time Senior Medical Director to produce key scientific content in a variety of therapeutic categories. As the Senior Medical  ...

Associate Director/Director CMC Regulatory Affairs - Boston

Company: TEC Group International
Location: Boston / Cambridge
Salary: Competitive
Benefits: competitive package
Closing Date: 16 Mar 17More Details
For more information or to apply for the position please contact Sam Murphy at the TEC Group International. 0208 544 3224 / sam.murphy@tecgroup.net

Head, R&D QA&C Analytics

Company: ProClinical Ltd
Location: Cambridge
Salary: Competitive
Closing Date: 02 Mar 17More Details
Our client, one of the biggest biotechnology companies in the world, is seeking a Head of R&D Quality & Compliance Analytics to join their team in Cambridge, MA. The company focuses on wide range of therapy areas including hematology, neuroscience, immunology and oncology. ...

Freelance Study Coordinator / Data Entry Coordinator: 1 month Contract

Company: CROMSOURCE
Location: California, United States
Salary: Negotiable
Closing Date: 16 Mar 17More Details
CROMSOURCE, a mid-sized family-owned CRO, is currently searching for a Study Coordinator / Data Entry Coordinator to join one of our partner companies in Duarte, California. This will be an office based, short term contract for 1 month to enter a backlog of data into an EDC System.

Senior Medical Writer

Company: CROMSOURCE
Location: Raleigh, United States
Salary: Negotiable
Closing Date: 16 Mar 17More Details
CROMSOURCE, a mid-sized family-owned CRO, is searching for an experienced Medical Writer to join our team in the US on a 12 month contract. This role will be part of our TalentSource division, where you will be permanently outsourced to a leading biopharmaceutical company. The ideal candidate will have strong Medical Writing skills, having wrote protocols, amendments and module 2 documents.

Program Manager, Quality Transformation

Company: ProClinical Ltd
Location: Somerville
Salary: Competitive
Closing Date: 02 Mar 17More Details
ProClinical has a brilliant opportunity for a Program Manager of Quality Transformation to be based in Somerville, New Jersey. This Program Manager job will be with one of the largest workforce management solutions companies in the world who specialise in multiple scientific and engineering sectors. Job Role:This Program Manager role will support the Quality Transformation Initiative for the strategic alignment of the client's medical device franchise. ...

Global Labeling Lead

Company: ProClinical Ltd
Location: New York
Salary: Competitive
Closing Date: 02 Mar 17More Details
A mid-sized pharmaceutical, headquartered in India, is seeking a Global Labeling Lead to based at their offices in New York, USA. Position Purpose: The Global Labeling Lead job holder has overall accountability for the initial creation and relevant updates to labeling documents for their assigned products. ...

Principal Statistical Programmer- New Jersey, USA

Company: RBW Consulting
Salary: Competitive
Closing Date: 16 Mar 17More Details
If you are interested in becoming part of a creative and dynamic team, then get in touch to find out more about this evolving company.

CRA role with Medical Device company

Company: EPM Scientific
Location: New York
Salary: 100,000+
Closing Date: 02 Mar 17More Details
We are seeking a CRA Role With Medical Device Startup! You will be responsible for monitoring activities across numerous sites on the East Coast.Qualifications:...

Director, Regulatory Affairs Advertising and Promotion

Company: Skills Alliance
Location: New Jersey
Salary: 100,000+
Benefits: Bonus
Closing Date: 01 Mar 17More Details
A global specialty pharmaceutical company in New Jersey is currently seeking a Director, Regulatory Affairs Advertising and Promotion to provide strategic guidance for the review...

Regulatory Affairs Consultant-Medical Devices

Company: Hydrogen Group
Location: California
Salary: Negotiable
Benefits: Negotiable
Closing Date: 22 Feb 17More Details
Regulatory Affairs Consultant-Medical Devices- California, USA Level: Regulatory Affairs Consultant-Medical Devices , Invitro Diagnostics (IVD) Contract: Minimum 2 Month Contract Salary: Negotiable Location: California, USA Summary Experienced Regulatory Affairs consultant required to manage regulatory activities for the US market. ...

Director, Medical Monitoring - Oncology

Company: ProClinical Ltd
Location: Philadelphia
Salary: Competitive
Closing Date: 01 Mar 17More Details
ProClinical is currently supporting a leading Clinical Research Organisation (CRO), who is recruiting for a Director, Medical Monitoring and Consulting. This is a permanent position based in Philadelphia, USA.Job Role Overview: This Director of Medical Monitoring will involve acting as Medical Monitor for numerous Oncology trials. ...

Clinical Research scientist - New Jersey - Global Pharma - Permanent Role - HOT JOB

Company: Meet
Salary: Competitive
Closing Date: 15 Mar 17More Details
My client is a global pharmaceutical company based in New Jersey, who are looking to grow their headcount due to their robust pipeline in the Oncology space. They are looking for a Clinical Research Scientist to join their team, on a permanent basis.

Senior Analyst – Global Value & Access - NJ

Company: Meet
Salary: Competitive
Closing Date: 15 Mar 17More Details
The individual needs to be an experienced Senior Analyst in HEOR and able to work in a global team in New jersey

This organization is a global pharmaceutical company based in New Jersey. They are making big hires across their growing HEOR team due to some big projects being won across the business. The individual will work in the global values team.

Director – Global Value & Access - New Jersey Global pharma

Company: Meet
Salary: Competitive
Closing Date: 15 Mar 17More Details
The individual needs to be an experienced Director in HEOR and able to work in a global team in New jersey

This organization is a global pharmaceutical company based in New Jersey. They are making big hires across their growing HEOR team due to some big projects being won across the business. The individual will work in the global values team.

Senior Manager – Global Value & Access - NJ

Company: Meet
Salary: Competitive
Closing Date: 15 Mar 17More Details
The individual needs to be an experienced Senior Manager in HEOR and able to work in a global team in New jersey

This organization is a global pharmaceutical company based in New Jersey. They are making big hires across their growing HEOR team due to some big projects being won across the business. The individual will work in the global values team.

Analyst – Life sciences Consulting New York - MUST BE BASED IN NYC AREA

Company: Meet
Salary: Competitive
Closing Date: 15 Mar 17More Details
The boutique consultancy is a HEOR strategy consultancy who focus on working with pharmaceutical and biotech companies across the USA.

The analyst position is an exciting new role in a growing team looking to further their career in the life sciences industry.

Statistical Programmer I/II

Company: SynteractHCR Deutschland GmbH
Location: Carlsbad, CA
Salary: On Application
Benefits: Excellent
Closing Date: 20 Feb 17More Details
Overview Provides programming support with supervision to the biostatistics and clinical programming functions. Develop, create, verify/validate and maintain managing the programs for assigned projects in compliance with standard operating procedures.   Responsibilities Creates/maintains analyses, tables/listings/figures Performs programming validation/QC Creates specifications for, and program derived datasets Provides ad-hoc reports as requested Assists...

Statistical Programmer I/II

Company: SynteractHCR Deutschland GmbH
Location: Morrisville, NC
Salary: On Application
Benefits: Excellent
Closing Date: 20 Feb 17More Details
Overview Provides programming support with supervision to the biostatistics and clinical programming functions. Develop, create, verify/validate and maintain managing the programs for assigned projects in compliance with standard operating procedures.   Responsibilities Creates/maintains analyses, tables/listings/figures Performs programming validation/QC Creates specifications for, and program derived datasets Provides ad-hoc reports as requested Assists...

Contract Clinical Program Manager - Princeton, NJ

Company: Barrington James Clinical
Location: Princeton, NJ
Salary: Competitive
Closing Date: 14 Mar 17More Details
I am working with a global pharmaceutical sponsor to find a Program Manager to act as a central contact for information on a particular program and manage activities to develop and commercialize programs. This person will ensure that team and line management concurrence is reached on program objectives and meets the planned objectives to achieve the organization’s goals of timely and quality-focused development of new therapies and life-cycle extensions within the portfolio.

Regulatory Technical Writer/Labeler

Company: Skills Alliance
Location: North Carolina
Salary: Negotiable
Closing Date: 28 Feb 17More Details
*Contract to Perm opportunity*Regulatory Technical Writer/Labeler- niche therapeutic medical device companyPosition Requirements: MUST have medical device experienceExtensive experience preparying regulatory submissions for...

Regulatory Affairs Specialist

Company: Skills Alliance
Location: North Carolina
Salary: Negotiable
Closing Date: 28 Feb 17More Details
*Contract to Perm opportunity*Regulatory Affairs Specialist - niche therapeutic medical device companyPosition Requirements: MUST have medical device experience within international countries.This candidate must...
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