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Job Details

Project Specialist - Amsterdam

Company: INC Research
Location: Amsterdam
Reference: 17003578
Closing Date: 20 Dec 17
Type: Permanent
Salary (£): Negotiable

Job Summary:

Join an industry-changing company that is reinventing the way we develop and commercialize drugs. At INC Research/inVentiv Health our 22,000 employees have one purpose: shortening the distance from lab to life.


We understand that cancer is not one disease, but a category of widely varying diseases, each with its own specialized scientific complexities, patient populations and range of treatment options. Our Oncology and Hematology practice is dedicated to the execution of clinical trials in these complex indications and is staffed by dedicated professionals with backgrounds in oncology drug development in academia, industry and CRO settings. This expertise, combined with our Trusted Process® methodology for delivering dependable trial outcomes, provides the resources, clinical expertise and development know-how to help our clients with every facet of their Oncology research

We are currently seeking a Project Specialist to support the contracted services and expectations of clinical studies assigned to the project team. This position is located in either in our Camberley or Edinburgh office.

A brief summary of duties you will be involved in:

• Tracks, processes and analysis clinical information relating to regulatory documents, adverse/serious adverse events, supplies, protocol deviations, IRB approvals, data queries
• Supports the Project Manager with financial aspects such as customer invoices and resource expenses; review of financial reports and analysis of upcoming project events.
• Oversees all regulatory documentation
• Preparation and attendance at Investigator meetings, Kick off meetings, Quick Start Camps and Quality Finish Camps
• Preparation and distribution of all meetings minutes, following up on action points
• Assist with training of new employees to assigned projects




This position requires the following skills and experience:

• Degree educated in the science/healthcare field, nursing degree, or equivalent combination of education and experience
• Experience of working in a CRO preferable
• Effective communication and customer interfacing skills
• Basic understanding and knowledge of ongoing protocol and disease related terminology, FDA regulations, GCP/ICH guidelines, drug development process for assigned study, as well as company and sponsor SOPs and WIs
• Strong attention to detail, organizational and problem solving skills
• Ability to perform several tasks simultaneously to meet deadlines
• Self-motivation and ability to work independently

Why choose us:
It takes skill and passion to develop medicines the way we do. Don’t worry – if you’ve got the passion part, we’ll help you develop the skills you need to enhance every aspect of your career in the clinical research industry.
We’ve got an attitude at INC: “Can do, I own it.” Absolutely everyone has ownership of what they do here. And because we’re given the freedom and responsibility to really own our projects, we can take them to new levels. And that means we can take our careers wherever we want them, too.
“We were ranked “Top CRO” to work with in the CenterWatch 2013 Investigative Site Relationship Survey (a biannual survey of over 2,000 sites worldwide).”

What happens next:
If your application is successful you will be contacted by one of our dedicated recruiters who will arrange a suitable date and time to speak to you further about this opportunity.

Apply for this job: Project Specialist - Amsterdam

Contact Information:

Address:  INC Research Europe
Királyhágó tér 8-9, 2th floor, 1126 Budapest, Hungary
Tel:  +36 1 489 48 56
Website:  Visit Our Web Site

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