Global Medical Affairs Manager

WORKING AT MÖLNLYCKE
Are you looking for a great career and want to make your mark?
Please keep on reading but don’t just take our word for it. We’ve interviewed colleagues around the world about their jobs, the Mölnlycke unique culture and Mölnlycke people and it is simply A great company to work for!
Could you help improve healthcare outcomes around the world?
If the answer is yes, you think just like us and should apply for this exciting opportunity that we have below.
We are currently recruiting for a Global Medical Affairs Manager to join our Medical Affairs department. The role is to be performed remotely. The purpose of the role is to own the indication(s) of the assigned products/product categories and is the medical-scientific link between the healthcare community and MHC. The position serves to support the three strategic pillars of the medical affairs department, within the respective gloves and ORS business areas:
Evidence generation
Evidence dissemination
Customer engagement

The Medical Affairs Manager role is responsible for providing strategic and operational support of business area stakeholders and demonstrate leadership to guide the completion of key evidence pieces to support the commercial strategy. At times, the role will work collaboratively with other business areas to deliver on “one-Molnlycke” initiatives. The Medical Affairs Manager conducts engagements with internal and external customers by role modeling Mölnlycke’s high performance behaviors, displaying integrity and a non-judgmental, positive attitude. In addition, the role participates in business development activities when requested by the medical director.

KEY ACCOUNTABILITIES
Develops a working knowledge and understanding of customer needs in target markets. This may include a healthcare provider (HCP), patients, procurement/value analysis professionals and other key customers as relevant to the strategy
Is considered an internal expert on business area product related evidence and is a resource for clinical discussions of appropriate use based on specific product indications
Builds long term relationships with key opinion leaders in target markets which support or expand current therapeutic concepts and ensure safe and appropriate utilization of products
Ensures adherence to relevant Regulatory requirements, Good Clinical Practice and Company Standard Operating Procedures as appropriate
Challenge, innovate and inspire new ways of working, especially those that improve the efficiency, effectiveness and cost-effectiveness of strategic initiatives set forth by the medical director
Provide creative insights into novel areas of geo-expansion, new market development and associated evidence needs, including identification of key opinion leaders

KEY DECISIONS
Identifies qualified key opinion leaders to support strategic initiatives and determines fair-market-value
Identify and grade strength of evidence of appropriate literature associated with support of the business strategy
Direct and support the publication process including manuscript creation, determination of authorship and selection of peer reviewed journals for the placement and dissemination of key study results to support commercial strategy
Collaborate with the global evidence committee to review, score and approve/decline quality improvement projects (QIPs) based on applicable global and regional regulations separating human subjects research from quality assurance and performance improvement activities

CAPABILITIES; QUALIFICATIONS AND EXPERIENCE
Clinical/scientific background (MD, DO, PharmD, PhD, RN) with 3+ years of experience in Pharmaceutical or Medical Device Industry (medical affairs preferred).
Capability to critically appraise, interpret and communicate research studies and scientific information
Experience in the design, implementation or execution of clinical trials and/or in vitro studies is preferred
Capability to independently develop and implement strategic action plans for evidence generation and evidence dissemination
Proficiency in the English language and excellent communication skills
Capability to develop and present oral presentations to key stakeholders when appropriate for internal or external training
Leadership capabilities to manage, lead and engage internal and external stakeholders

OTHER INFORMATION
Location: Remote
There is no specific geographic office assignment for this position (EU or US is preferred)
The Medical Affairs Manager may work remotely per the established global guidance on remote working principles
International travel is required to support the business areas in strategic areas of focus, to engage with key opinion leaders and support appropriate clinical congresses
The Medical Affairs Manager may follow global guidance on flexible working hours especially when business activities involve regions in different time zones


Applicants will be reviewed continuously, please apply at your earliest convenience.
About Mölnlycke
Mölnlycke is a world-leading medical solutions company. We design and supply solutions to enhance performance at every point of care – from the hospital to the home proven it every day.
We specialise in:
•Wound management: including dressings with Safetac® such as Mepitel® and Mepilex®
•Preventing pressure ulcers: with Mepilex® Border used prophylactically and devices to help turn and re-position patients
•Surgical solutions: including Mölnlycke trays, HiBi® antiseptics and Biogel® surgical gloves
Mölnlycke was founded in 1849. Nowadays our solutions are available in around 100 countries; we’re the number one global provider of advanced wound care and single-use surgical products; and we’re Europe’s largest provider of customised trays. Our headquarters are in Gothenburg, Sweden and we have about 7,800 employees around the world.