Would you like to become a leader in LINK Medical Regulatory Department?
- Arbeidsgiver
- LINK Medical Research
- Stillingstittel
- Regulatory Group Lead
- Frist
- Snarest
- Ansettelsesform
- Fast
This position is open at our office in Oslo, Norway.
LINK Medical is searching for a motivational and inspiring Regulatory Group Lead to develop and lead one of our teams within regulatory affairs. As a Regulatory Group Lead you will be a member of the Regulatory Management Team, and an important contributor to the development of our people and processes. You will be highly involved in the day to day administration of the department and the team members. We are looking for candidates with considerable competence within regulatory affairs for medicinal products and a person that believes that the best results are achieved through motivated people and teams. We are preferably searching for candidates with management experience, but we will also consider strong candidates without this experience.
You will work with a broad portifolio of customers and therapy areas in all phases of development. As a leader in LINK Medical you will deliver high quality services in accordance with our customer expectations. You will have the opportunity to develop your competence and leadership skills together with other talented leaders. You will also have the opportunity to learn how to implement solutions according to our customer needs and participate in activities related to business development.
Desired qualifications:
- Natural science degree at college/university level
- Minimum 5 years experience within Regulatory Affairs
- Management experience preferred
- Generally good IT skills
- Fluent in Norwegian and English (written and oral)
Personal characteristics:
- Ability to motivate others and to build successful teams
- Likes to build personal relations and to influence others
- Result oriented
- Solution oriented
- Excellent communication skills
Responsibilities:
- Ensuring that staff is motivated and competent
- Ensuring that staff conducts assignments according to agreements
- General supervising within relevant fields
- Active project participation
- Ensuring customers’ positive perception of the collaboration with LINK Medical
- Establishing and maintaining customer contact to get new assignments
- Participate in planning the department’s actions and in resource allocation
- Promote the market position of LINK Medical
- Active participation in the department’s management team
- Cooperation with colleagues in LINK Medical, nationally and internationally
Contact information:
If you would like to know more or have any questions about the position, please contact Grethe Berven, Director Regulatory & Safety in Norway, phone no. +47 920 25 155.
All applications are treated confidentially.
Last day for application: 30. November 2019
Om arbeidsgiveren
LINK Medical is a full-service contract research organization (CRO) providing product development services for the pharmaceutical and medical device industries across Northern Europe. Our Scandinavian roots and culture provide a high-quality service delivery based on respect, work integrity and a strong focus on solutions. We are a pragmatic problem-solver, empowering our experienced specialists with modern technology that will change your expectations of a CRO partner. Our promise is to improve and accelerate your product development through transformative methods, active communication and optimal solutions.
- Sektor
- Privat
- Lederkategori
- Leder
- Sted
- Gjerdrums vei 19, 0484 Oslo
- Bransje
- Farmasi og legemiddel
- Stillingsfunksjon
- Konsulent,
- Ledelse
Nøkkelord
Regulatory Affairs, Management, Business development, Motivator, Team builder
Spørsmål om stillingen
- Kontaktperson
- Grethe Berven
- Stillingstittel
- Director Regulatory & Safety
- Mobil
- 92 02 51 55
Gjerdrums vei 19, 0484 Oslo