Medical director Ledige stillinger

Genmab is focused on the creation and development of innovative and differentiated antibody products, with the aim of improving the lives of cancer patients. The Role We are looking for an experienced and dedicated Associate Medical Director to be a part of our Global Clinical Development Team (Hematology). The Associate Medical Director will be accountable for the medical oversight of one or more clinical trials, medical review and communication of data, and medical input into regulatory documents and presentations. This is a full time position that can be located either in Princeton NJ or Copenhagen DK. Partial remote/partial onsite work. Responsibilities: Directing study design, protocol development and execution of clinical research for pivotal cancer studies. Contributing to the overall medical strategy of the assigned clinical development programs and product pipeline as well as giving in-depth medical advice on potential new projects (internal and external)....

At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives. Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development. That’s our vision. We’re driven by it. And we need talented people who share it. If you’re as driven as we are, join us. You’ll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you’ll be helping shape an industry. The Role: Medical Director Rheumatology within ICON - This is an exciting opportunity to work within a fast-paced environment within a...

Genmab is focused on the creation and development of innovative and differentiated antibody products, with the aim of improving the lives of cancer patients. The Role We are looking for an experienced and dedicated (Associate) Medical Director to be a part of our Global Clinical Development Team (Hematology). AS (Associate) Medical Director will be accountable for the medical oversight of one or more clinical trials, medical review and communication of data, and medical input into regulatory documents and presentations. This is a full time position that can be located either in Utrecht, NL or Copenhagen DK. Responsibilities: Directing study design, protocol development and execution of clinical research for pivotal cancer studies. Contributing to the overall medical strategy of the assigned clinical development programs and product pipeline as well as giving in-depth medical advice on potential new projects (internal and external). Generating/reviewing clinical components of key...

The Role: Medical Director Rheumatology within ICON - This is an exciting opportunity to work within a fast-paced environment within a culture derived from collaboration, partnership and accountability. ICON is a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. Responsibilities include: Providing medical leadership on project teams Providing medical I scientific consultation and therapeutic expertise Overseeing study specific medical/safety monitoring activities, ensuring compliance with ethical, legal, and regulatory standards as well as ICON and Sponsor SOPs Representing the Medical Affairs Department in business development activities Providing functional/departmental oversight in the absence of Senior Medical Director I Vice President, Medical Affairs Requirements for the role include: 5 plus years' experience in Rheumatology and a board certification in Rheumatology 2-3 plus years' experience in...

Senior International Medical Director to evaluate and plan new indications for CagriSema We are looking for a medical doctor (MD) with broad experience in clinical drug development, preferably supported by translational research and business development expertise, to evaluate and plan new therapeutic indications for CagriSema and support research activities in Amylin biology. The Department To accelerate and expand the promising novel therapy CagriSema, a dedicated area has been established as part of Clinical Drug Development located in Søborg, Copenhagen, Denmark. In Medical & Science, we are medically responsible for the clinical development program. Our responsibilities include planning and execution of clinical trials (phases 1-4) and non-interventional studies, medical and scientific support to health authority interactions, publications, early research activities, presentations, and more. You will be joining an area of 11 medical doctors and 3 clinical pharmacologists, and we...

International Medical Director Are you a medical doctor (MD) with a background of drug development and medical/ research experience preferably within the field of cardiovascular disease? This could be an exciting opportunity for you! We need your analytical skills and research experience to drive novel trial designs and your clinical experience to support ongoing development of innovative treatment options that will make a difference for patients. You thrive in navigating the many interdependencies of clinical drug development evaluating competing priorities and risks while facilitating clear communication and decision-making. Join us and you will be part of a team of talented colleagues in a great and inspiring working environment. The position Successful candidates are dedicated team players who can analyse and communicate data which can be used to design trials, ensure medically sound regulatory interactions as well as to drive learnings one step further into implementation and...

The job requires a high degree of independence and team spirit as many decisions have high business impact. Therefore, focus as well as flexibility is important due to several tasks will be coming from different stakeholders and expectation management is key to success. Your Qualifications You must hold a university degree as a Medical Doctor, have experience with drug development and medical expertise in pharma/biotech industry. Having a PhD and clinical and/or drug development experience in endocrine diseases and especially in rare endocrine diseases is seen as an advantage. We work in a global environment hence proficiency in English is needed and you should expect travelling activities of approximately 15-20 days per year. Working at Novo Nordisk Novo Nordisk Rare Disease is a speciality care unit focused on generating scientific and technological breakthroughs for people living with a rare and ultra-rare diseases. We have a 40-year legacy and expertise in rare blood and...

The job requires a high degree of independence and team spirit as many decisions have high business impact. Therefore, focus as well as flexibility is important due to several tasks will be coming from different stakeholders and expectation management is key to success. Your Qualifications You must hold a university degree as a Medical Doctor, have experience with drug development and medical expertise in pharma/biotech industry. Having a PhD and clinical and/or drug development experience in endocrine diseases and especially in rare endocrine diseases is seen as an advantage. We work in a global environment hence proficiency in English is needed and you should expect travelling activities of approximately 15-20 days per year. Working at Novo Nordisk Novo Nordisk Rare Disease is a speciality care unit focused on generating scientific and technological breakthroughs for people living with a rare and ultra-rare diseases. We have a 40-year legacy and expertise in rare blood and...

Your role As a Medical Expert working on a development project within dermatology, you will join an ambitious, fun-loving, and closely collaborating team of Medical Expert colleagues, striving to bring innovative treatments to patients with dermatological conditions. You will also work in cross-functional teams together with colleagues from other skill areas. Your primary tasks will, depending on your level of experience, be to: Advance our drug development projects together with your team and identify solutions to the various challenges that arise along the way Shape the strategic development of our drug development projects by driving the medical and scientific content of the Clinical Development Plan Help deliver on the Clinical Development Plan by being responsible for the medical input to clinical trials from the very beginning, through the design, conduct and reporting of the trials. This involves working on trial protocols, trial reports, regulatory documents, investigator’s...

Job Profile Responsibilities include to: Create and guide clinical development plans for selected projects, in close collaboration with project teams Work in accordance with applicable guidelines and regulatory plans/regulatory advice to ultimately support marketing authorizations Provide relevant post-approval medical and life-cycle support Create clinical trial outlines ensuring fit for purpose design excellence in accordance with strategy and the needs of early and late-stage drug development projects Support execution of the strategy and other project related tasks on-time and with the highest quality Support the clinical team in executing the clinical development plan Act as Zealand’s medical expert for selected clinical projects and trials Ensure proper medical monitoring, including when the role is delegated to appropriately qualified medical personnel, such as outside consultants or CROs in accordance with SOPs Provide medical subject matter expertise to the clinical and...

Audigy is a management company that provides business services for ENT and audiology practices across the nation. Audigy’s Mission is to help our Members achieve their personal, professional, and financial goals by delivering unparalleled growth, leadership and a commitment to the success of every practice we serve. Why work at Audigy? We are making a difference to small business owners all over the country and into Canada. We are leveling the playing field so that small medical practices can compete with the big box retailers in providing small business jobs to their communities and ultimately by providing top of the line quality hearing care to their patients. Pay range $26.44-$31.51 per hour, DOE, as well as the following benefits: Our Benefits Include: 401k w/company match Parental/Family Leave w/transition back to work Medical/Dental/Vision Hybrid work environment Top technology platforms for easy remote access Day Care Flexible Spending...

Are you looking for an exciting student position within data analytics in a world leading global company on a strong growth journey? Then you might be our new colleague. Join the world’s oldest start-up and turn up the volume on your career At GN we design and manufactures world-leading intelligent audio and video communication solutions. We have consumer, professional and medical-grade products and expertise, all under one roof. Inspired by people and driven by our passion for innovation, we leverage technologies to deliver unique user experiences that bring people closer through the power of sound. GN's market leading solutions are marketed under brands such as ReSound, Beltone, Interton, SteelSeries, Jabra, BlueParrott and FalCom in more than 100 countries. GN Group employs over 7000 people and is listed on Nasdaq Copenhagen (GN.CO). GN Audio – home of Jabra, BlueParrott and SteelSeries Through its Jabra, BlueParrott and SteelSeries brands, GN works to lead...

Genmab is focused on the creation and development of innovative and differentiated antibody products, with the aim of improving the lives of cancer patients. The Role As Associate Director, you will become part of the Global Drug Safety and Pharmacovigilance department, where you will be responsible for drug related activities in close cooperation with the Safety Physicians. This position has a global perspective, and you will interact with stakeholders ranging from regulatory authorities and DMCs as well as colleagues from other Genmab sites. As Associate Director, Global Drug Safety and Pharmacovigilance Scientist, you will be part of a highly skilled and international team. The position reports to the Project Safety Physician Lead. Responsibilities Perform safety review of Adverse Event reports for Genmab products Perform ongoing surveillance (including signal detection/evaluation) of safety data from Genmab clinical trials Be the safety contact for other departments and ensure...

Do you have what it takes to manage stakeholders and drive projects, acting as the link between clinical development and commercial marketing? Then join us and work with some of the best and most engaged colleagues in the Medtech industry as our new Medical Specialist. “We provide the strong link between our clinical departments and our commercial business, driving the clinical agenda by KOL partnerships, evidence generation and clinical education to provide the best possible user outcome”, says Iben Plate, Director, Evidence & Adoption, Medical Affairs. Listen, learn and collaborate to make a difference The Evidence and Adoption department is a diverse group of highly experienced specialists, who take great professional pride in delivering quality to, learning from and collaborating with our customers and the Coloplast organisation. You will be the local medical strategy expert supporting Marketing, HCP education as well as Coloplast subsidiaries. You will manage a variety of...

Do you want to help us raise the standard of care for our users in China? Then join us and become our local medical strategy expert – an important role where you use your knowledge of Chinese culture as you manage projects and create medical evidence to better the lives of users of intimate healthcare products. “This agenda is strategically important because there is an unmet need for people with intimate health care needs in China. And since you will become a key driver in this effort, you have a great chance to leave your mark and ultimately make a difference for millions of people,” Iben Plate, Senior Director, Evidence & Adoption explains. Welcome to Evidence & Adoption You will be a part of the Coloplast Evidence & Adoption Team located in Humlebæk, Denmark. We are responsible for supporting the organisation with our highly specialised knowledge and for shaping the clinical ambition of our business to increase the relevance of existing and new products and services. We are a...

Join the world’s oldest start-up and turn up the volume on your career Are you a structural wiz, a stickler for rules and an expert on labelling? Then you may just be the one to help ensure that labels, packaging and user manuals for our hearing aids and their accessories meet all regulations. In this key role, you get to make your mark on a new and still growing team – not to mention the way we work with labelling. Welcome to a vibrant documentation department At GN, we lead major technology shifts with intelligent audio solutions. At our HQ in Ballerup, you will be joining 4 technical writers, 1 fellow regulatory labelling specialist and 1 documentation manager. Together, we ensure a high-quality customer experience by making labels and user guides for our hearing aids. We are a diverse and cooperative bunch of specialists who always strive towards creating better structures for our work. And though we work with different areas of responsibility, we endeavor...

BACKGROUND OF THE APPOINTMENT The appointment is for a newly established marketing role that will focus on driving sell-out of Jabra (and BlueParrott) product lines through key retail channels – both online and offline – across Japan and elevating Jabra market share in the region. The role will require close working alignment with the regional & local-market retail & online sales leadership. GN Audio (Jabra/BlueParrott) is looking to strengthen its Retail & Online Marketing (i.e., Consumer Marketing) team in Japan; introducing increased online/digital and channel/trade marketing capability to accelerate retail partner marketing engagement and deliver best-in-class launch and in-life marketing programs for its family of wireless (and true wireless) headphones/earbuds. Consequently, GN Audio (Jabra/BlueParrott) is looking for a consumer marketer with proven track-record within CE across the region. ORGANIZATIONAL PLACEMENT / REFERENCE CRITERIA As a Sr. Marketing...

Graphic Designer (full-time consultant) Job Description Beltone is seeking a Graphic Designer to support our in-house marketing team. The ideal candidate must be able to work as part of a team to develop communications for various multi-media campaigns and create other brand and promotional support assets as needed.  As one of our “in-house” Graphic Designers, you’ll help bring to life our brand position, “Right Beside You” for patients and prospective patients, as well as our network of clinic owners and hearing care practitioners.  You will visualize and create graphics for print and digital/social ads, point of sale materials, websites, product packaging, exhibitions, logos and more. Not only will your work allow Beltone to capture the attention of those who see it, you get to play a key role in helping people hear and live better. This position reports to the Director of Marketing Operations and requires a strong work partnership with the Marketing, Field marketing...

Position: Quality Data Analyst (Quality Specialist) Reports to Title: Head of NA Product Quality Department/Division: Product Quality North America Primary Work Location: Bloomington, MN or Home Office (US) Revision Date: May 2022     Position Overview Provide data retrieval and consolidation from relevant sources to drive insights and analysis into reasons for NA customer product quality complaints and returns.  Contribute to improvements in product quality and related processes and reduction in cost of poor quality through direct involvement and hands on investigations of product HW, SW and system complaints. Essential Functions (Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.) Monitoring and reporting on NA product quality data and trends and identification of top issues Creation and communication of knowledge articles Performance measurement and quality reporting Preparation of...

POSITION DESCRIPTION Position:  Inside Sales Representative (ISR) Reports to Title:  Inside Sales Manager Department/Division:  Sales Primary Work Location:  Bloomington, MN Job Code/Classification : Non-Exempt Revision Date:  December 2022 There are currently two open Inside Sales Representative positions. This position will be located in our Bloomington office with the ability to work from home on occasion. Position Overview The Inside Sales Representative sells GN ReSound branded and Private Label hearing aids to audiologists, dispensers, physicians, hospitals, and other hearing healthcare professionals. This is done primarily over the telephone.  Builds and maintains customer relationships to grow current customer’s business. Essential Functions (Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.) Reach or exceed territory sales goals on a monthly, quarterly and annual basis via:...