Recordati
Medical Science Liaison, Endocrinology (Atlanta, GA)
Recordati, Bridgewater, Massachusetts, us, 02324
Medical Science Liaison, Endocrinology (Atlanta, GA)
This position is with Recordati Rare Diseases, Inc. (RRD), North America, an affiliate of Recordati.
Recordati Rare Diseases, Inc. (RRD) develops high-impact 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: Associate Director, Medical Affairs or designee
Direct Reports: None
Areas Managed: Medical Affairs Initiatives
Overview The Medical Science Liaison (MSL) will serve as our field-based scientific expert whose mission is to foster collaborative relationships with opinion leaders focused on Cushing’s Syndrome, Cushing’s Disease, and Acromegaly 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 peer- to-peer liaison internally and externally.
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 up-to-date medical information, robust diseases expertise, and product information.
Provide scientific support at medical conferences and support medical community with up-to-date medical information and robust Cushing’s Syndrome, Cushing’s Disease, and Acromegaly understanding and product information for Isturisa, Signifor, and Signifor LAR.
Maintain peer-to-peer 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-initiated trials as well as company-sponsored research.
Support clinical initiatives including assessment and selection of clinical investigations, site identification, registry and presentation of final approved data.
Provide medical and scientific input into the planning and execution of Advisory Boards. Work with physician 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.
Responsible for developing territory plan with input from direct line manager.
Gather clinical field insights and inform team on a regular basis through appropriate channels.
Understand the role and contributions provided by Medical Science Liaisons and Medical Affairs.
Act in full compliance with all laws, regulations, and policies including adverse events/pharmacovigilance responsibilities.
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).
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.
Location/Travel
This position is field-based, 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 accommodations for qualified individuals 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.
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Recordati Rare Diseases, Inc. (RRD) develops high-impact 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: Associate Director, Medical Affairs or designee
Direct Reports: None
Areas Managed: Medical Affairs Initiatives
Overview The Medical Science Liaison (MSL) will serve as our field-based scientific expert whose mission is to foster collaborative relationships with opinion leaders focused on Cushing’s Syndrome, Cushing’s Disease, and Acromegaly 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 peer- to-peer liaison internally and externally.
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 up-to-date medical information, robust diseases expertise, and product information.
Provide scientific support at medical conferences and support medical community with up-to-date medical information and robust Cushing’s Syndrome, Cushing’s Disease, and Acromegaly understanding and product information for Isturisa, Signifor, and Signifor LAR.
Maintain peer-to-peer 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-initiated trials as well as company-sponsored research.
Support clinical initiatives including assessment and selection of clinical investigations, site identification, registry and presentation of final approved data.
Provide medical and scientific input into the planning and execution of Advisory Boards. Work with physician 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.
Responsible for developing territory plan with input from direct line manager.
Gather clinical field insights and inform team on a regular basis through appropriate channels.
Understand the role and contributions provided by Medical Science Liaisons and Medical Affairs.
Act in full compliance with all laws, regulations, and policies including adverse events/pharmacovigilance responsibilities.
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).
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.
Location/Travel
This position is field-based, 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 accommodations for qualified individuals 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.
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