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Y-mAbs Therapeutics A/S, Hørsholm
Y-mAbs Therapeutics A/S (Y-mAbs) is now looking for an Associate Director/Director of Corporate Drug safety (CDS). In this newly established position, you will report to the Senior Director, CDS.
Y-mAbs is an international biotech company (listed on Nasdaq) with two late stage development programs and an exciting pipeline. Y-mAbs also initiates several new clinical trials in both Europe and US this year. Furthermore, Y-mAbs aims for regulatory submissions of our two most advanced late stage programs within a short time frame.
- Execute drug safety oversight for the clinical projects
- Perform medical assessment of reported SAEs
- Perform overall safety surveillance/risk management activities for Y-mAbs' products
LEO Pharma, Ballerup
Do you want to work with drug safety in clinical development?
As Senior Safety Advisor you will be a key player in the safety surveillance and development of one of LEO Pharma’s new biologics Tralokinumab for the treatment of atopic dermatitis.
We are offering a job with considerable individual responsibility, challenges, and the opportunity to develop your professional and personal competencies. As Senior Safety Advisor, your main focus is to be globally responsible for effective safety risk management processes with main tasks being:
- Signal detection and management
- Participation in clinical trial teams providing safety input to clinical development discussions and documents, e.g. trial protocols and Investigator’s Brochure
- Preparation of safety input to various regulatory documents
LEO Pharma, Ballerup
Do you want to take on responsibility for a challenging task of scientific/medical support of LEO Pharma’s well-established brands?
You will become a part of Region INTERNATIONAL, one of three business critical regions in LEO Pharma. Together with other Scientific Affairs Manager(s) you will share the global responsibilities for some of LEO Pharma’s well-established brands and regional responsibilities for selected products marketed in Region International.
You will develop the global Scientific Affairs programs and activities and at the same time work closely with our regional markets, while meeting with Medical Thought Leaders (MTL) at regional advisory boards and gaining hands-on insights on local patient needs and therapeutic practices. You will ensure that these insights are incorporated into the Global and Regional Strategies, Operation Plans and Life Cycle Management activities.
Ferring Pharmaceuticals A/S, Copenhagen
Driven by research and a passion for science Ferring Pharmaceuticals is a biopharmaceutical company dedicated to the development of innovative treatments that make a real difference in people’s lives all over the world. Active in the areas of reproductive health, urology, gastroenterology, endocrinology and orthopaedics, we develop medicine on the body's own terms. We believe in the power of people and research - and go where ideas and research take us.
As a Medical Device Safety Medical Writer, you will primarily be responsible for coordinating, planning and preparing CEP´s and CER´s, giving input to risk management files as well as to clinical questions. When the new MDR legislation is fully enforced during 2020, the work will also encompass writing PSUR´s/Post Market Surveillance Reports and Post Market Surveillance Plans on Ferring medical devices.
We offer an opportunity to join a pharmaceutical company focusing on brain diseases and influence the development strategy for our pipeline projects. The position is based at our headquarters in Copenhagen, reporting to Director, Head of Medical Affairs Psychiatry, Pipeline.
In the position you will provide medical expertise and insights into different cross-functional pipeline projects. In projects in the early development phase, your input is key for selecting the indication(s) to pursue for further development. In projects in later phase of development you will be responsible for the scientific communication strategy and the publication plan.
United Nations Development Programme, Copenhagen
We are looking for a General Practitioner at UN City in Copenhagen for three days a week.
You will service a cliental coming from very diverse backgrounds. The personnel at the UN City comes from all corners of the world and have rich experiences from living and working in different cultures. They are specialised or trained in varying disciplines such as medical, security, environmental policies, finance etc. While very diverse they all share a dedication to making a difference to achieve the goals and objectives of UN.
The work entails:
- Provide primary care
- Provide preventative medical actions
- Provide vaccinations and travel advice
Senior Specialist Pharmacovigilance
Zealand Pharma A/S, Glostrup
Are you passionate about making a true difference for patients with rare diseases? Are you also thinking of making a career change and be part of a very dynamic, ambitious, professional, yet lean and agile team where you can have influence?
Then you may be our new colleague in Regulatory, Pharmacovigilance and Medical Writing.
Zealand Pharma A/S (Zealand) is looking for a Pharmacovigilance Senior Specialist who will report to the Head of Pharmacovigilance. This is a new position.
The Senior Specialist will have as key responsibilities:
- Ongoing safety surveillance
- Signal management
- Aggregated safety reporting
DIS- Study Abroad in Scandinavia is seeking a Lab instructor with strong knowledge of E-Prime, SPSS and basic statistics to assist primarily American undergraduate university students enrolled in a research-based course.
- Minimum 80 hours per semester with the possibility to increase
- Exciting, international educational environment
- Salary by AC agreement
We offer a challenging and exciting international educational environment with a strong focus on our highly motivated American undergraduate students as well as excellent support from our Teaching & Learning department. You will be working in a dynamic environment together with a dedicated academic faculty and staff where emphasis is on academic quality, cross-cultural understanding, teamwork, innovation and adaptability.
Radiometer Medical ApS, Brønshøj
Do you have a fascination with critical care and medical devices? Then Radiometer is the perfect destination for you to expand and share clinical knowledge internally and with external experts.
Your responsibilities include:
- Proactively develop scientific proof sources concerning the clinical use of our Immunoassay products
- Defining and driving new initiatives that can further strengthen our medical, clinical and scientific footprint in the marketplace including the development of future products and services from Radiometer
- Establishing relations to health care professionals and key external experts worldwide, including initiating and contributing to studies
The job requires travelling between 20 to 40 days a year to attend congresses, customer meeting etc. thereby building strong professional expertise in the relevant clinical fields.