Director Safety
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København K
This position is open at our offices in Copenhagen, Denmark or Malmö, Sweden.
LINK Medical is searching for a Director Safety. Our company is growing, and the portfolio of cross-functional projects is increasing. As a Director Safety, you will lead the safety function in LINK Medical and will report to the Executive Vice President Regulatory & Safety. You will work in close collaboration with members of internal and external project teams, with local and international projects, and within a range of different therapeutic areas.
We offer an exciting and challenging position in a European CRO and Regulatory Service provider that has a strong local presence. The company focuses on collaboration, sharing of experience and continuous development of our employees. You will be given engaging assignments requiring efficient collaboration with industry partners, clinical and scientific teams and the regulatory authorities. We offer a competitive compensation and benefit scheme for all employees.
Contact information
If you would like to know more or have any questions about the position, please contact Executive Vice President Regulatory & Safety, Hilde K Holme, phone +47 93 44 89 75.
All applications are treated confidentially.
Last day for submitting your application: 2023-10-27.
We are handling this recruitment within LINK Medical Research and kindly ask of external recruiters not to contact us to offer your services.
Please apply to the job by filling out the application below:
-- Current status of employment --Employed full timeEmployed part timeNot currently employed
Resume
Cover Letter
I have read and accept the Privacy Policy
LINK Medical is searching for a Director Safety. Our company is growing, and the portfolio of cross-functional projects is increasing. As a Director Safety, you will lead the safety function in LINK Medical and will report to the Executive Vice President Regulatory & Safety. You will work in close collaboration with members of internal and external project teams, with local and international projects, and within a range of different therapeutic areas.
Responsibilities
- Provide leadership and consultancy to clients and project teams delivering services in the areas of safety & pharmacovigilance, device vigilance, veterinary vigilance, medical information and product complaints.
- Support the strategic and operational functions of the safety department to meet its goals and project objectives.
- System owner for the safety database and ensure the further development of the database.
- Provide oversight to safety teams and contribute to project deliverables in the areas under safety.
- Develop, improve, and implement processes for effective safety management.
- Create an environment that encourages learning, self-improvement, and career development for staff.
- Contributes to the implementation of sales & marketing strategies (e.g. for new service offerings or specific target clients).
- Participates in developing new and existing business by interacting with clients.
- Maintain familiarity with current industry practices and regulatory requirements that affect benefit/risk evaluations, NDAs/BLAs/MAAs, and changes to labeling and marketing authorization.
- Maintain professional knowledge and relevant accreditation by active participation in continuing education activities.
Desired qualifications
- Strong experience in safety management (expert level)
- Health care professional degree
- Experience in a leadership position including functional management.
- Thorough understanding of safety operations and global regulatory requirements.
- Excellent written and oral communication and presentation skills.
- Reads, writes, and speaks English; fluent in a Scandinavian language required.
- Experience managing professional staff; managing clinical research staff highly preferred (performance management, 1:1s, goal setting, and other HR processes).
- To qualify, applicants must be legally authorized to work in the EU/EEA, and should not require, now or in the future, sponsorship for employment visa status.
Preferred:
- An advanced degree (M.Sc., M.D. or Ph.D.) from an accredited institution in medicine, pharmacy or other life sciences preferred.
- Experience in system implementation
- Experience in implementing new safety services or functions in an organization.
Personal characteristics
- Takes initiative, acts with confidence, and works independently.
- Initiates and generates activity, internally and externally.
- Makes prompt, clear decisions which may involve tough choices or considered risks.
- Likes to lead, provides others with a clear direction and delegates work appropriately and fairly.
- Demonstrates an interest in and understanding of others, motivates and builds team spirit.
- Works strategically to realize organizational goals.
- Identifies and creates business opportunities for the organization.
- Produces the highest quality work, while maintaining professionalism, and courteous attitude with clients and fellow team members
LINK Medical offers
We offer an exciting and challenging position in a European CRO and Regulatory Service provider that has a strong local presence. The company focuses on collaboration, sharing of experience and continuous development of our employees. You will be given engaging assignments requiring efficient collaboration with industry partners, clinical and scientific teams and the regulatory authorities. We offer a competitive compensation and benefit scheme for all employees.
Contact information
If you would like to know more or have any questions about the position, please contact Executive Vice President Regulatory & Safety, Hilde K Holme, phone +47 93 44 89 75.
All applications are treated confidentially.
Last day for submitting your application: 2023-10-27.
We are handling this recruitment within LINK Medical Research and kindly ask of external recruiters not to contact us to offer your services.
Please apply to the job by filling out the application below:
-- Current status of employment --Employed full timeEmployed part timeNot currently employed
Resume
Cover Letter
I have read and accept the Privacy Policy
Information og data
Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".
Arbejdsstedet er beliggende i København K.
Jobbet er oprettet på vores service den 16.10.2023, men kan have været deaktiveret og genaktiveret igen.
Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
- Øvrige
- København K
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