Senior Manager, Medical Affairs
ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
The Therapeutic Area Lead Solid Tumors is part of the Medical Affairs Team and provides a bridge between Clinical Development, Medical Affairs, and the commercial organization
What You Will Do:
Your focus will be involved in a wide range of activities for inline and pipeline products. This is a very diverse role and a unique opportunity where you can cover the whole spectrum of drug development
Key responsibilities include:
Constantly builds and maintains expertise in the assigned areas (tumor entities, products), regarding available literature, treatment options, disease environment and product data, key contact for training and all educational approaches.
Gains in-depth knowledge in early development indications and analyzes different data sources resulting in meaningful reports and derived strategies.
Identifies and engages with internal and external experts when appropriate, for participation in medical communications as well as consultants for content development, when necessary
Provides oversight and contributes to the preparation and delivery of high-quality content and all educational and medical communication materials (e.g. planning for medical society presence, abstracts, and publications)
Streamlines product communication, works with external and internal resources on the development of multi-channel communication strategies and materials (for internal and field/external use) and medical event planning
Acts as medical point of contact for clinical studies within solid tumor indications and provides continuous support to study centers and the ClinOps Team
Your Profile:
You will have a strong background in medical affairs, with proven management experience and a commitment to quality delivery.
Required qualifications and experience:
MD, PharmD or PhD in life sciences
Long standing experience in the pharmaceutical industry, preferably in oncology
5-7 years of relevant working experience in similar roles
Proven track record in preparing for product launches and successful life cycle management
Knowledge in development and implementation of clinical trials
Experienced in material review in the role of an Information Officer
Excellent communication skills and ability to present scientific data
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Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Rewards & Benefits
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include:
Benefits may vary depending on role and location.
Visit our careers site to read more about the benefits ICON offers.
Inclusion and Accessibility
ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
If you require reasonable accommodations during the recruitment process, please let us know or submit a request here
Are you a current ICON Employee? Please click here to apply
Since our foundation in Dublin, Ireland in 1990, our mission has been to help our clients to accelerate the development of drugs and devices that save lives and improve quality of life. We do this by delivering best in class information, solutions and performance, with an unyielding focus on quality at all times.
We offer a full range of consulting, development and commercialisation services from a global network of offices in 53 countries. We focus our innovation on the factors that are critical to our clients – reducing time to market, reducing cost, and increasing quality – and our global team of experts has extensive experience in a broad range of therapeutic areas.
