Regional Medical Affairs Manager / Sr. Regional Medical Affairs Manager (LA at Gossamer Bio

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Full Time

Start Date

Immediate

Expiry Date

19 Dec, 25

Salary

0.0

Posted On

20 Sep, 25

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Pulmonary Hypertension, Clinical Trials, Scientific Expertise, Relationship Building, Strategic Leadership, Medical Affairs, Cross-Functional Collaboration, Education Initiatives, Competitive Intelligence, Presentation Skills, Analytical Skills, Communication Skills, Project Management, Adaptability, Team Collaboration, Patient Enrollment

Industry

Biotechnology Research

Description

Summary: The Regional Medical Affairs Manager / Sr Regional Medical Affairs Manager will be responsible for facilitating scientific exchange and clinical support for Gossamer’s clinical studies and will engage with clinical study sites, investigators, and study personnel to encourage fast study start up, identification of patients, and enrollment efforts in Gossamer Bio’s company sponsored studies. Essential Duties and Responsibilities: Strategic & Scientific Leadership Demonstrate deep scientific expertise in pulmonary hypertension (PAH/PH-ILD) and related therapeutic areas to inform strategy and external engagement. Distill feedback from healthcare providers (HCPs) and investigators into actionable insights to shape cross-functional strategy. Contribute to the development of medical and scientific materials, ensuring accuracy, high quality, and alignment with corporate standards. Participate in advisory boards, internal project teams, and therapeutic area strategy discussions. Execute strategic medical affairs initiatives in support of department priorities as assigned by management. Function as lead on assigned projects within medical affairs (competitive intelligence, Veeva, Journal Club, etc) External Engagement & Relationship Building Develop and maintain trusted relationships with principal investigators, key opinion leaders (KOLs), advocacy groups, and other external experts. Educate and support clinical sites on trial protocols, enrollment, and patient retention, in collaboration with Clinical Operations. Deliver high-quality scientific and educational presentations to diverse audiences. Represent the company at national/regional congresses, symposia, and scientific meetings, gathering insights on the competitive and treatment landscape. Serve as a liaison between the scientific community and the company to enhance understanding of scientific foundations and goals for approved, in-development, and active trials sponsored by the company and its partners. Cross-Functional Collaboration Partner with Medical Monitors, Clinical Development Leads, Clinical Operations, and Medical Science Liaisons (MSLs) to ensure coordinated trial and field execution. Support HCP and site staff education on clinical protocols and the scientific rationale. Contribute to the development and execution of strategic KOL engagement plans. Provide medical and scientific support in response to unsolicited questions from HCPs, payers, and decision makers. Provide therapeutic area expertise to cross-functional partners (Marketing, Sales, Market Access, etc) Collaborate with partners on medical affairs projects that are co-branded Education, Insights & Value Delivery Coordinate scientific education initiatives for external stakeholders, including advocacy groups and HCPs. Provide clinical and economic value information to payers and formulary decision makers. Gather and communicate competitive intelligence, research developments, and treatment advances to internal stakeholders. Compliance & Administration Ensure timely, accurate completion of administrative reports and documentation. Provide guidance on the investigator-initiated study (IIS) process and facilitate communication of review outcomes. Ensure all medical activities adhere to regulations and promote ethical standards Consistently model company values, fostering openness, innovation, and collaboration. JOB QUALIFICATIONS Advanced scientific or clinical degree (PhD, PharmD, DNP, MD, DO or equivalent strongly preferred). Minimum 2+ years of experience in a field-based Medical Affairs role; experience in PAH and/or PH-ILD strongly preferred. 5+ years of experience for a senior level. Broader experience in cardiovascular, pulmonary, transplant, or critical care will be considered. Clinical trial experience required, with strong understanding of trial design, site operations, and enrollment dynamics. Experience with pre-launch, launch, and post-launch activities. Proven ability to build and sustain relationships with principal investigators, KOLs, and other external experts to support clinical trial execution and scientific exchange. Demonstrated ability to translate complex scientific data into clear, impactful communications for a range of stakeholders. Strong analytical skills with the ability to collect, distill, and communicate medical insights that shape cross-functional strategy. Strong organizational skills, able to manage competing priorities and timelines in a dynamic environment. Strong presentation and teaching skills, with the ability to tailor content to audience needs and facilitate discussions. Excellent communicator, skilled at diplomacy and capable of combining scientific expertise with relationship building. Adaptability to a changing scientific and clinical landscape; ability to pivot strategies as new information emerges. Collaborative mindset with demonstrated success working across Clinical Development, Clinical Operations, Commercial, and other internal partners. Self-directed with a strong leadership presence, able to represent the company at conferences, advisory boards, and other scientific forums. Ability to work independently and manage multiple responsibilities both internally and externally Must be willing to travel extensively, including occasional weekends. Office environment / Domestic and International travel up to 75% may be necessary. Territory encompasses a broad geographical area across Mexico and potentially surrounding LATAM regions. Candidate must reside in Mexico. Gossamer Bio is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants and complies with all applicable national, state and local laws governing nondiscrimination in employment. California Consumer Privacy Act (CCPA) Notice for California Residents: This notice is to notify you that personal data about you has been collected by Gossamer Bio (“Controller”), which is located at 3115 Merryfield Row, Suite 120, San Diego CA 92121 and can be contacted by emailing privacy@gossamerbio.com, because Controller wishes to evaluate your candidacy for employment at Controller. Your personal data was either obtained from publicly available sources (e.g. LinkedIn) or provided to Controller by someone who referred you for potential employment. Controller’s Privacy team can be contacted at privacy@gossamerbio.com. Your personal data will be processed for the purposes of managing Controller’s recruitment related activities, which include setting up and conducting interviews and tests for applicants, evaluating and assessing the results thereto, and as is otherwise needed in the recruitment and hiring processes. Such processing is legally permissible under Art. 6(1)(f) of Regulation (EU) 2016/679 (General Data Protection Regulation) and the California Consumer Privacy Act (CCPA) as necessary for the purposes of the legitimate interests pursued by the Controller, which are the solicitation, evaluation, and selection of applicants for employment. Your personal data has been shared with Greenhouse Software, Inc., a cloud services provider located in the United States of America and engaged by Controller to help manage its recruitment and hiring process on Controller’s behalf. Your personal data will be retained by Controller as long as Controller determines it is necessary to evaluate your application for employment. Under the GDPR and CCPA, you have the right to request access to your personal data, to request that your personal data be rectified or erased, and to request that processing of your personal data be restricted. You also have to right to data portability. In addition, you may lodge a complaint with a supervisory authority.

Responsibilities

The Regional Medical Affairs Manager will facilitate scientific exchange and clinical support for Gossamer’s clinical studies, engaging with clinical study sites and investigators to enhance patient enrollment efforts. They will also develop relationships with key opinion leaders and provide medical insights to shape cross-functional strategies.