Medical Science Liaison

Company: Protara Therapeutics
Location: New York City
Posted on: July 10, 2025

Job Description:

Company Overview: Protara Therapeutics is a clinical-stage biotechnology company committed to advancing transformative therapies for people with cancer and rare diseases. Protara’s portfolio includes its lead candidate, TARA-002, an investigational cell-based therapy in development for the treatment of non-muscle invasive bladder cancer (NMIBC) and lymphatic malformations (LMs). The Company is evaluating TARA-002 in an ongoing Phase 2 trial in NMIBC patients with carcinoma in situ (CIS) who are unresponsive or naïve to treatment with Bacillus Calmette-Guérin (BCG), as well as a Phase 2 trial in pediatric patients with LMs. Additionally, Protara is developing IV Choline Chloride, an investigational phospholipid substrate replacement for patients on parenteral support who are otherwise unable to meet their choline needs via oral or enteral routes. Job Overview: The MSL develops ongoing professional relationships with national and regional healthcare opinion leaders and other healthcare professionals to provide medical and scientific support for company initiatives for TARA-002 in NMIBC. Territory: TBD based on where the team leader is located. Responsibilities Develop and maintain scientific, clinical, and technical expertise in NMIBC and across uro-oncology through ongoing training and self-education, including attendance at relevant conferences, scientific workshops, and review of key publications and resources. Support clinical trial execution, including recruitment and site outreach, as requested, and communicate feedback to the Clinical Operations and Clinical Development teams. Work collaboratively with the Clinical Operations and Clinical Development teams as requested. Build a territory plan for the assigned geography that includes strategies and tactics for engaging with HCPs/key opinion leaders (KOLs) at their respective institutions and medical congresses. Identify, establish, and maintain collaborative relationships with key investigators, institutional leaders, medical groups, and consortia. Provide scientific evidence and clinical trial information to healthcare professionals, clinical trial staff, and payors in a clear, scientifically accurate, and balanced manner. Increase awareness in the medical community of the company and enhance company interaction with thought leaders. Assist in training of new hire MSLs and, as appropriate and assist in design and implementation of effective training curricula and field resources that will promote the company’s reputation as a patient-oriented and science-driven organization; a reliable source of balanced medical information; and a partner in education and research with health care providers (HCPs) engaged in treating patients with rare and oncologic diseases. Support the development and implementation of advisory boards and other scientific meetings. Present scientific data at these forums as requested. Monitor the competitive landscape for specific therapeutic areas of interest to the company, including current disease management strategies, approved products, new/emerging therapies, and differentiating features of approved/emerging competitor products. Contribute to the CI plan for medical congresses. Communicate insights back to the company effectively, especially those that may pertain to ongoing and planned clinical trials. Execute MSL activities with adherence to all related policies and standard operating procedures, and with regulatory and other ethical guidelines relevant to the pharmaceutical industry. Address unsolicited medical questions related to clinical trials, Investigator Initiated Research Studies, and other scientific exchange. Qualifications Advanced clinical/science degree or professional credentials required (MD/DO, PhD, PharmD, PA, NP, RN). 5 years of experience in the biotech or pharmaceutical industry, preferably in Medical Affairs, with 3 years’ MSL experience and working with internal cross-functional teams. Urology experience required; Uro-oncology experience prioritized. Must have expertise in the bladder cancer space. Must have strong connections in the NMIBC space. Excellent interpersonal skills, including the ability to communicate effectively with diverse audiences and build strong relationships. Must have clinical trial and launch experience. Drive for personal excellence and accountability; set these expectations for the field team and promote the same for Medical Affairs colleagues. Business/enterprise mindset. Possess creative problem-solving skills. Strong interpersonal skills and demonstrated ability to work collaboratively in a dynamic, team-oriented environment. Strong organizational and business planning skills, including development of strategic plans and budgets, and adherence to targets. Ability to interact and communicate openly and effectively with Management, team members, HCPs/TLs, nurse coordinators and other clinical trial site staff, and payors. Experience conducting formal scientific presentations. Strong analytical skills, especially regarding understanding and interpreting scientific and clinical research and literature are essential. Adept, nimble, energetic, and comfortable in a fast-paced, dynamic, and collaborative environment Capable of, and motivated by, taking a hands-on approach and "rolling up one's sleeves." Extensive travel (up to approx. 60%, US and international) with possible weekend congress obligations. Physical Demands: The physical demands here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Average travel for this position is 50% with some variations based on the demands of the business needs. Must be willing to travel to clinical trial sites, and vendors as applicable. Work Environment: The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. No specific work demands. To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed above are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. *Salary Requirements are between $170,000 - $195,000 based on experience and qualifications. Why You’ll Love Working at Protara Friendly, open, and fun team-oriented culture that values unique & diverse perspectives. Company-wide dedication to profoundly impacting patients’ lives. Amazing culture whereby core values and behaviors are shared cross-functionally. Competitive Salary and Benefits package includes incentive bonus, equity compensation, medical, dental, vision, commuter, and fertility benefits. Matching 401(k) Retirement Plan. Flexible working hours/schedule. Generous Paid Holidays and Unlimited PTO. Protara is committed to being a diverse and inclusive workplace. Protara is an Equal Opportunity Employer and is committed in policy and in practice to recruit, hire, train, and promote in all job qualifications without regard to race, color, creed, religion, national or ethnic origin, citizenship status, age, sex or gender, gender identity or expression (including transgender status), sexual orientation, marital status, military service and veteran status, disability, genetic information or any other characteristic protected by applicable federal, state or local laws.

Keywords: Protara Therapeutics, Sayreville , Medical Science Liaison, Science, Research & Development , New York City, New Jersey