Medical Affairs Pharmacist

Company Overview

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.

Job Summary

TheMedical Affairs Pharmacistserves as the organizations primary clinical and scientific expert supporting medical information internal education and external scientific engagement across bothsterile 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 organizations scientific credibility and clinical leadership.

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

Qualifications

Required

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 ofpresentation 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)

Physical Requirements

• Ability to sit for extended periods of time at a desk and working on a computer

• Ability to communicate effectively in person over the phone or via virtual meeting

• Ability to maintain focus in a typical office environment with moderate noise levels

• Ability to perform repetitive motions with hands and arms such as typing.

Southend Pharmacyis unable to offer visa sponsorship at this time. Candidates must be legally authorized to work in the United States without current or future sponsorship.

Equal Opportunity Employer Statement

Allia Health Group is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race color religion gender gender identity or expression sexual orientation national origin genetics disability age or veteran status.

If you have any questions or require accommodations during the application process please contact.