Medical Science Liaison Oncology and Hematology Baltimore MD OR Washington

With its beginnings in a family run pharmacy in Correggio Italy in the 1920s Recordati is now a global pharmaceutical company listed on the Italian stock exchange with over 4500 employees and turnover of over Euro 2bn.

We are a group of likeminded passionate individuals who go to extraordinary lengths for our patients customers partners investors and the people across the globe who we serve. We develop and commercialise medicines to serve people living with common diseases as well as those living with some of the rarest in around 150 countries.

At Recordati our mantra is simple. We’ve always believed that health and the opportunity to live life to the fullest is a right not a privilege. Whether that is for common diseases or the rarest – we want to give people the opportunity to be the best version of themselves.

This drive will never stop. Together we will always be reimagining tomorrow – with new ideas new technologies and new innovations to fight diseases.

Recordati. Unlocking the full potential of life.

This position is with Recordati Rare Diseases Inc. (RRD) North America an affiliate of Recordati.

Recordati Rare Diseases Inc. (RRD) develops highimpact therapies for rare diseases focusing on providing treatments to underserved communities in the U.S. Our mission is to mitigate the impact of rare diseases through increased awareness better diagnoses and improved treatment access in endocrinology metabolic hematology and oncology franchises. RRD is dedicated to fostering a dynamic work environment that promotes professional growth and a significant impact on patients' lives.

Reporting Structure

Reports To: Director Medical Affairs or designee

Direct Reports: None

Areas Managed: Medical Affairs Initiatives

Overview

The Medical Science Liaison (MSL) will serve as our fieldbased scientific expert whose mission is to foster collaborative relationships with opinion leaders and to facilitate the exchange of unbiased scientific information between the medical community and the company. The MSL will have the clinical/medical affairs expertise to serve as a peertopeer liaison internally and externally.

Essential Duties And Responsibilities

• Deliver clinical and scientific presentations to health care professionals including clinicians (i.e Endocrinologists etc.) and P&T committee members. Support medical community with uptodate medical information robust diseases expertise and product information.
• Provide scientific support at medical conferences.
• Develop and maintain peertopeer collaborations and relationships with key medical experts in relevant therapeutic areas.
• Respond to unsolicited medical information requests using a customized approach.
• Collaborate with physicians on medical affairs initiatives including providing assistance with publications and investigator sponsored studies as well as company sponsored research.
• Support clinical initiatives including assessment and selection of clinical investigators site identification registry and presentation of final approved data.
• Provide medical and scientific input into the planning and execution of Advisory Boards. Work with physicians experts to review speaker presentations and provide medical references when requested.
• Train staff including sales team on key scientific and medical topics in relevant therapeutic areas.
• Participate in the development and review of professional slide decks medical letters and clinical summaries.
• Maintain compliance with all internal and external legal and regulatory guidelines.
• Gathers clinical field insights and informs team on a regular basis through appropriate channels.
• Understand the role and contributions provided by Medical Science Liaisons and Medical Affairs.
• Perform additional duties as may be assigned.

Education And Experience

• Advanced scientific degree (M.D. D.O. Ph.D. Pharm.D.) in Medical Biological Sciences required.
• Minimum of two years of experience in Medical Affairs/Clinical functions strongly preferred.
• Familiarization with drug development process FDA ICH and GCP guidelines.
• Experience implementing monitoring and/or managing clinical trials for academic clinical research or pharmaceutical/biotechnology company a plus.

Knowledge And Skills

• Ability to review and interpret clinical data.
• Ability to develop clinical data and medical content for presentation to internal and external audiences
• Proficient in Microsoft Office suite of products (e.g. Word PowerPoint Excel).
• Strong presentation skills.
• Project management experience a plus.
• Experience with rare diseases a plus (including Medical Affairs clinical practice research).
• Excellent time management and ability to work independently.
• Excellent written and verbal communication skills.

Competencies and Attributes

• Behaves in an honest fair and ethical manner.
• Pursues selfdevelopment.
• Communicates in a clear concise and convincing manner. Listens effectively.
• Strong relationship building skills
• May be called on to assist in developing new members of the company.
• Responsible for tactical implementation of predefined programs and projects.
• Solves issues of moderate complexity.
• Works independently on issues where analysis of situation or data requires evaluation of different factors.
• Monitors expenditures.

Work Environment

This job operates in a professional office environment. This role routinely uses standard office equipment such as computers phones photocopiers filing cabinets and fax machines. Based upon job requirements employee may be required at times to attend meetings including travel out of state over weekends and nights. Employee must be able to freely operate and travel by car and train/plane modes of transportation. Employee is required to have a valid driver’s license and means of transportation.

Physical Demands

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. The employee must be able to fly via commercial air carrier.

This is largely a sedentary role; however the employee frequently is required to stand; walk; use hands to finger handle or feel; and reach with hands and arms; talk and hear. Occasionally is required to lift and/or move light to moderate weight up to 25 lbs.

Location/Travel

• This position is fieldbased near a major airport.
• Approximately 60% of travel required.

FLSA Classification

• This position is considered Exempt.

EEO Statement

It is the policy of Recordati Rare Diseases to provide equal employment opportunity (EEO) to all persons regardless of race color religion sex sexual orientation gender identity or national origin. Further Recordati Rare Diseases will not discriminate on the basis of any characteristic protected by federal state or local law. Recordati Rare Diseases will provide reasonable accommodate for qualified individual with disabilities.

Disclaimer

This job description is not designed to cover or contain a comprehensive listing of the activities duties or responsibilities that may be required.

At Recordati we believe in people! Inspired by our purpose unlocking the full potential of life we are committed to creating a diverse environment and cultivating a culture of inclusion. We strive to continually lead with our values and beliefs enabling our employees to bring their whole selves to work and develop their potential.

We are proud to be an equal opportunity employer. We recruit develop and reward without regard to amongst others gender sexual orientation gender identity or expression national origin age physical or mental ability race ethnicity political or religious belief.

If you are looking to join a company where you can try new things speak openly and be bold we invite you to apply today.