Labcorp is looking for a Clinical Project Leader in Norway to be 100% client dedicated with a top 10 Pharmaceutical company. The role involves the oversight and co-ordination of Clinical Projects across the Nordic and Baltic region, so a significant job! The successful candidate will have impact on both regulatory and financial compliance. Interestingly this role will cover all therapeutic areas outside of Oncology so Neurology, Cardiology, infectious disease, HIV and paediatrics.

What makes this opportunity special?

• You will be 100% client dedicated with a prestigious Pharmaceutical company.
• Career progression will be exceptional because there are lots of studies coming through in 2021 across a variety of therapeutic areas
• Your Line Manager will also be based in Norway and so ready to support if need be
• The working conditions within our Norwegian team are great! A very positive environment where everyone works together well and in harmony.
• The job is permanent, full time & 100% home-based (with the option of going into the Oslo office as much as you like).
• You will be joining a large team with a well organised structure and robust processes in place
• Competitive salary, car allowance and benefits package including.

The position requires strong leadership skills (scientific and business) and ability to coordinate and lead local teams to high performance. Oversee country commitments, compliance and training needs. Additionally, business leadership and alignment with corporate requires that individual has ability to lead across several dimensions simultaneously.

To apply please send your CV to andy.smith@covance.com or call Andy on +44 (0) 7775 848 250

Education/Qualifications: Minimum Required:

• University/college degree (life science preferred), or certification in a related allied health profession from an appropriately accredited institution, nursing certification, medical or laboratory technology
• In lieu of the above requirement, candidates with minimum of four (4) or more years of relevant clinical research experience in pharmaceutical or CRO industries or experience in a health care setting will be considered
• Thorough knowledge of ICH Guidelines and GCP including a basic understanding of regulatory requirements in other countries
• Thorough understanding of the drug development process
• Fluent in local office language and in English, both written and verbal

Experience: Minimum Required:

• Good organizational and time management skills
• Working knowledge of ICH, FDA, local regulatory requirements, IRB/IEC and other applicable regulations/guidelines; familiarity with investigator start up documents; previous interaction with operational project team and investigative sites preferred.
• Excellent communication skills, oral and written.
• Self-motivation with the ability to work under pressure to meet deadlines
• Works well independently as well as in team environment.
• Detail and process oriented
• Positive attitude and approach
• Interact with internal and external customers with high degree of professionalism and discretion
• Multi-tasking capability.
• Good computer skills with good working knowledge of a range of computer packages
• Ability to lead and develop junior staff
• Flexible and adaptable to a developing work environment

• Minimum of six-eight (6-8) years of clinical research experience