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Job matches 7

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Office Administrator

Company: CROMSOURCE
Location: United States
Salary: On Application
Benefits: Excellent and Comprehensive Benefits – see below
Closing Date: 22 Oct 17More Details
Office Administrator   Location: Waltham, MA   Driver's license required       CROMSOURCE is looking for a new team member that can provide office support. As an office administrator you would be required to wear many hats and jump in to help whenever needed! The CROMSOURCE office is an intimate office environment where teamwork is valued because we are continuously growing.

Clinical Trial Administrator II

Company: CROMSOURCE
Location: United States
Salary: On Application
Benefits: Excellent and Comprehensive Benefits – see below
Closing Date: 22 Oct 17More Details
Clinical Trial Administrator II - Waltham, MA At CROMSOURCE, Clinical Trial Administrators (CTA) are key players in the success of our clinical trials. As a CTA you have the opportunity to be the main avenue of support for the clinical trial team. The CTA cooperates with the project team with accurately updating and maintaining clinical tracking systems as well as being responsible for the preparation, handling, distribution, collection, filing and archiving of clinical...

Clinical Lead

Company: CROMSOURCE
Location: United States
Salary: On Application
Benefits: Excellent and Comprehensive Benefits – see below
Closing Date: 22 Oct 17More Details
 
Clinical Lead (CL)
 
We are working with a client to support an upcoming Phase III coeliac trial in the US, which will start soon.  We are currently looking for a complete team for the study including a full-time Clinical Leads (CL).  This is a home based role located anywhere in the US as long as you are close to a central airport and have good links to many US locations.

Clinical Trial Administrator

Company: CROMSOURCE
Location: United States
Salary: On Application
Benefits: Excellent and Comprehensive Benefits – see below
Closing Date: 22 Oct 17More Details
Top Job
Clinical Trial Administrator
Waltham (MA)
Schedule: Full time, 40 hours a week
CROMSOURCE is a family owned international, full-service Contract Research Organisation who, since 1994, has been supporting our clients with outstanding clinical research and staffing solutions services. We are currently recruiting for a team of staff (CTAs through to Project Managers) to join us for the start of an exciting suite of studies in the respiratory area.

Summary:

Clinical Trial Administrator
Waltham (MA)
Schedule: Full time, 40 hours a week
CROMSOURCE is a family owned international, full-service Contract Research Organisation who, since 1994, has been supporting our clients with outstanding clinical research and staffing solutions services. We are currently recruiting for a team of staff (CTAs through to Project Managers) to join us for the start of an exciting suite of studies in the respiratory area.

Clinical Project Manager

Company: CROMSOURCE
Location: United States
Salary: On Application
Benefits: Excellent and Comprehensive Benefits – see below
Closing Date: 22 Oct 17More Details
Project Manager– Waltham, MA
At CROMSOURCE, the Project Manager is working directly on a variety of clinical trials. As a PM, you must have some experience working in a similar role – supporting the management of clinical projects. The PM manages the clinical projects ensuring quality of the services in accordance with contractual obligations, applicable SOPs, ICH/GCP guidelines and other applicable regulations.

Senior Clinical Project Manager

Company: CROMSOURCE
Location: United States
Salary: On Application
Benefits: Excellent and Comprehensive Benefits – see below
Closing Date: 22 Oct 17More Details
Top Job
Senior Clinical Project Manager (SPM) – Waltham, MA
CROMSOURCE is looking for an expert project manager with over 10 years’ experience in the CRO/Pharmaceutical industry. As a project manager you are responsible for supervising the assigned clinical research projects. The SPM manages the correct development of the clinical project, interacting with the Sponsor and the Investigators and properly coordinating the project team members! We are looking for someone who has...

Summary:

Senior Clinical Project Manager (SPM) – Waltham, MA
CROMSOURCE is looking for an expert project manager with over 10 years’ experience in the CRO/Pharmaceutical industry. As a project manager you are responsible for supervising the assigned clinical research projects. The SPM manages the correct development of the clinical project, interacting with the Sponsor and the Investigators and properly coordinating the project team members! We are looking for someone who has...

Clinical Project Coordinator

Company: CROMSOURCE
Location: United States
Salary: On Application
Benefits: Excellent and Comprehensive Benefits – see below
Closing Date: 22 Oct 17More Details
Project Coordinator – Waltham, MA
At CROMSOUCE, the Project Coordinator is working directly with the Project Managers on a variety of clinical trials. As a PC, you must have some experience working in a similar role – supporting the management of clinical projects. The PC manages the clinical projects ensuring quality of the services in accordance with contractual obligations, applicable SOPs, ICH/GCP guidelines and other applicable regulations.
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