Project Managers, Clinical Trial Services

Klifo

Join a dynamic and experienced team
KLIFO is expanding and is looking for 2 new Project Managers to join a dynamic and experienced team within Clinical Trial Services. The people we want to engage thrive in a consulting environment and have a positive, proactive, flexible, self-driven and self-confident personality. We can offer a highly flexible, free and trustful working climate with exciting projects among competent colleagues where your contribution is valuable and makes a difference.

Project management and scientific inputs
With a direct report to the Clinical Research Director, the Project Manager (PM) is overall responsible for managing the clinical trials in all phases, from start-up to the end of the trial. This include leadership of people involved in the project (CRAs, CTA, etc.) and investigational site selection to assuring the quality and conformity of the sites. It also includes the more scientific areas such as operational and scientific input to key project documents.

We have a broad variety of clients, and you will therefore get the opportunity to work on exciting projects for a heterogeneous client pool (Pharmaceutical companies, established Biotech, inexperienced Biotech, investigators/academia)

Experienced and flexible
You hold a MSc. in the life sciences field combined with a minimum of 5-6 years of overall experience out of which a minimum of 2 years must be in project management in the pharmaceutical industry from a Biotech or from a CRO. You have extensive knowledge of GCP guidelines, applicable regulatory requirements, medical terminology and clinical trial processes. We will further expect you to have documented project management skills including the ability to plan a project and operate according to timeline, plan and budget. Furthermore, we expect you to have excellent verbal and written communication skills in English and in one of the Scandinavian languages.

Unique company culture with influence and flexibility
KLIFO offers a very interesting job opportunity in a unique company culture with a high level of transparency, influence and possibility for individual planning. With our broad and differentiated client base, you will get the opportunity to use and elaborate your competences and experience in an interactive and positive working environment.

How to apply
The recruitment process is carried out in collaboration with the consulting company Compass Human Resources Group A/S. Please submit your CV and application in English on www.compasshrg.com – If you would like to find out more about this position before submitting your application, please do not hesitate to contact Senior Research Consultant Joan Hemmingsen or Partner Morten Islin on tel.: +45 70 20 12 75. Please note that we will reply to the email address from which you send your CV.

KLIFO is a service provider of drug development competences and operational services to the Pharmaceutical, Biotech and Med-tech companies in Europe, US and Asia. The areas covered by KLIFO include Clinical Trial Supply, Clinical Trial Services, Pharmacovigilance, Regulatory Affairs and Drug Development Counselling. KLIFO is located in Smedeland 36, 2600 Glostrup. Further information about KLIFO can be found at www.klifo.dk.

Deadline for application: As soon as possible
Workplace:
Glostrup
Reference: 
1703.352
Company: 
Klifo

Contact: