Medical Affairs Pharmacist - Hybrid

Medical Affairs Pharmacist

Southend Pharmacy is a modern 503A compounding pharmacy built on clinical precision, operational clarity, and a human-first approach. Licensed in 35+ states and focused on longevity-aligned therapeutics, we support providers and their patients with precision in compounding and transparent processes. Southend Pharmacy operates at the intersection of innovation, ambition, and clinical excellenceblending precision, clarity, and compassionate support to help providers deliver patient-centered, clinically guided care across every step of the treatment journey.

The Medical Affairs Pharmacist serves as the organization's primary clinical and scientific expert, supporting medical information, internal education, and external scientific engagement across both sterile and nonsterile compounding. This role is responsible for delivering accurate, evidence-based medical information, leading internal clinical training initiatives, and supporting compliant scientific exchange with healthcare professionals. This position will expand to include conference attendance and Medical Science Liaisonstyle activities, supporting the organization's scientific credibility and clinical leadership.

Hybrid Opportunity

Hybrid Work Schedule: This position offers a hybrid work environment with three (3) days onsite and two (2) days remote per week following successful completion of our required onsite training program.

IMPORTANT TRAINING REQUIREMENT: All candidates must be available to complete three (3) consecutive weeks of mandatory onsite training, Monday through Friday. This initial training period is fully onsite and non-negotiable, regardless of the position's hybrid schedule.

Key Responsibilities

Medical Information & Clinical Support

Serve as the primary medical information resource for internal teams and external healthcare professionals

Provide medical information support for sterile and nonsterile compounded preparations. Respond to clinical inquiries related to:

Formulation rationale and excipient selection

Dosing, administration, and route-specific considerations

Stability, beyond-use dating, and storage

Sterility assurance principles and risk-based decision-making

Safety, contraindications, and special population considerations

Research, analyze, and synthesize scientific literature to ensure medical responses are accurate, evidence-based, and clinically appropriate

Develop, review, and maintain medical information resources, including: Standard response documents

Clinical FAQs and reference guides

Literature reviews and scientific summaries

Ensure all medical information content aligns with applicable regulatory, accreditation, and quality standards for compounding pharmacies (e.g., USP <795> , <797> , <800> , as applicable)

Track inquiry trends to proactively identify knowledge gaps and develop supporting clinical content

Monitor and stay current on evolving regulatory, accreditation, and professional standards impacting sterile and nonsterile compounding, including updates to USP chapters, FDA guidance, and relevant state board requirements, and incorporate changes into medical information content and clinical guidance

Internal Medical Training & Education

Design and deliver internal clinical and medical training programs for pharmacy staff, customer-facing teams, and leadership

Support onboarding and ongoing education related to:

Sterile and nonsterile compounded product offerings

Therapeutic areas supported by the pharmacy

Clinical rationale behind formulation and beyond-use dating decisions

Develop and maintain training materials, including slide decks, quick-reference tools, and clinical playbooks

Lead recurring educational sessions such as lunch-and-learns, clinical updates, and ad hoc trainings

Collaborate closely with pharmacy operations, quality, and compliance teams to ensure consistent and compliant medical messaging

Continuously update training content based on evolving clinical evidence, regulatory changes, and internal feedback

Proactively update internal training materials and educational programs to reflect changes in regulatory standards, compounding guidance, and best practices, ensuring continued inspection and audit readiness

Scientific & External Engagement

Participate in medical and pharmacy conferences to support scientific exchange and professional development

Engage in compliant scientific discussions with healthcare professionals regarding: Appropriate use of sterile and nonsterile compounded therapies

Clinical decision-making when commercially available products are not suitable

Build and maintain professional relationships with pharmacists, prescribers, and key clinical stakeholders

Gather and communicate medical insights from external engagements to inform internal education, strategy, and operations

Cross-Functional Collaboration

Partner with pharmacy operations, quality, compliance, and leadership teams to address complex clinical and formulation-related questions

Provide medical and scientific input to support strategic initiatives and clinical decision-making

Serve as a trusted internal advisor on sterile and nonsterile compounding-related clinical matters

Regulatory & Standards Awareness

Maintain ongoing awareness of changes to regulatory, accreditation, and professional standards affecting sterile and nonsterile compounding practices

Translate regulatory and standards updates into clear, clinically relevant guidance for internal stakeholders

Partner with Quality and Compliance teams to support consistent interpretation and application of updated requirements

Contribute to inspection and audit readiness by ensuring medical information content and clinical training reflect current expectations

What We Require

Doctor of Pharmacy (PharmD) from an accredited school of pharmacy

Active, unrestricted pharmacist license in good standing (multi-state licensure preferred or ability to obtain)

3+ years of progressive experience in clinical pharmacy, medical affairs, medical information, compounding pharmacy, or a related scientific or regulatory role

Demonstrated expertise in interpreting, evaluating, and synthesizing scientific literature to support evidence-based clinical and medical decision-making

Strong working knowledge of sterile and nonsterile compounding principles, including formulation science, excipient selection, stability, beyond-use dating, and sterility assurance

Working knowledge of regulatory and accreditation frameworks impacting compounding pharmacy (e.g., USP <795> , USP <797> , USP <800> , FDA guidance, and state board requirements)

Proven ability to develop, review, and maintain high-quality medical information content, including standard response documents, literature reviews, scientific summaries, and clinical reference materials

Experience responding to complex clinical inquiries related to dosing, administration, formulation rationale, safety considerations, contraindications, and special populations

Demonstrated ability to engage in compliant scientific exchange with healthcare professionals while maintaining adherence to medical, legal, and regulatory standards

Minimum of three years' experience of presentation and executive communication skills, with the ability to deliver compelling scientific and clinical content to healthcare professionals, leadership teams, and professional audiences

Proven experience and credibility representing an organization at medical, pharmacy, or scientific conferences, including participation in scientific dialogue and external engagement

Experience designing and delivering internal clinical education, medical training programs, or continuing education content for pharmacy and cross-functional teams

High ethical standards, sound clinical judgment, and a strong commitment to patient safety, scientific integrity, and regulatory compliance

Preferred

Prior experience in a Medical Affairs, Medical Science Liaison (MSL), Medical Information, or scientific communications role within healthcare, pharmaceuticals, or specialty pharmacy

Advanced experience in sterile compounding, complex formulations, or regulated compounding environments (503A and/or 503B preferred)

Demonstrated experience supporting scientific strategy, clinical positioning, or evidence-based education initiatives across cross-functional teams

Experience participating in national or regional medical, pharmacy, or scientific conferences as a clinical or scientific representative

Board certification, residency training, fellowship training, or advanced clinical specialization (e.g., BCPS, BCSCP, or relevant specialty credentials)

What We Offer

• Full benefits package including medical, vision, dental, 401(k) with company match, PTO, Flex days, holidays, and more!

Southend Pharmacy does not provide employment visa sponsorship now or in the future. Applicants must be legally authorized to work in the United States without the need for current or future sponsorship.

Equal Opportunity Employer Statement Southend Pharmacy is proud to be an Equal Opportunity Employer where we are committed to fostering a diverse and inclusive workplace. We are committed to cultivating a culture where all team members feel valued & respected. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender identity or expression, sexual orientation, national origin, genetic information, disability, age, veteran status, or any other characteristics protected by applicable law. If you have any questions or require immediate assistance or accommodations during the application or interview process, please contact us at View email address on click.appcast.io