Bridging Healthcare Expertise With Pharmaceutical Industry Capability
PharmaLink Academy was established to address a growing global challenge within the pharmaceutical industry: highly qualified healthcare and life science professionals often enter the sector without exposure to the operational, regulatory, and safety expectations required in practice.
Our mission is to develop industry‑ready professionals through capability pathways grounded in real pharmaceutical workflows, regulatory thinking, and applied experience.
Why PharmaLink Exists
Pharmaceutical development operates within highly regulated environments where documentation accuracy, safety evaluation, and cross‑functional collaboration directly influence patient outcomes.
While academic and clinical training produce knowledgeable professionals, many enter pharmaceutical environments without familiarity with regulatory workflows, safety systems, or industry decision‑making structures.
PharmaLink Academy was created to bridge this gap by translating scientific expertise into industry‑aligned capability.
Industry‑Led Approach
Our programmes are designed around how pharmaceutical organisations operate in reality. Participants engage with simulated regulatory and safety workflows, structured assignments, and expert feedback aligned with global industry expectations.
Rather than focusing solely on theoretical learning, PharmaLink emphasises applied reasoning, professional judgement, and operational understanding required within regulated environments.
Our Mission
To strengthen the pharmaceutical workforce by developing professionals who understand regulatory responsibility, safety culture, and industry collaboration from day one.
By bridging the gap between scientific education and pharmaceutical operations, PharmaLink contributes to a more capable, confident, and industry‑ready global workforce.
The People Behind PharmaLink Academy
PharmaLink Academy is supported by experienced regulatory writers, pharmacovigilance specialists, editors, and operational professionals who bring real‑world pharmaceutical expertise into every programme and learner interaction.
Megan Day
Regulatory Writing Expert Instructor
Megan Day is an experienced Regulatory Medical Writer with over 35 years experience and a strong track record of delivering high-quality clinical and regulatory documents for global pharmaceutical and biotech companies. She has worked across multiple stages of the drug development lifecycle, contributing to key submission documents including clinical study reports, protocols, investigator brochures, and regulatory modules aligned with ICH and global health authority requirements.
With a meticulous eye for detail and a deep understanding of regulatory expectations, Megan brings real-world industry rigour into her teaching. Her approach is practical, structured, and grounded in how regulatory medical writing is actually executed within fast-paced cross-functional teams.
Sandhyaa Subramanian
Regulatory Writing Expert Instructor
Sandhyaa Subramanian is one of our a medical writer's who supports students with assignments and feedback. She completed a Master's degree in Biomedical Sciences from University of Glasgow and prior to becoming a regulatory medical writer was working as a research associate.
She made the transition, as they say - " from lab bench to medical writing desk" and since then has worked as a regulatory medical writer for the past 2 years with experience across various documents such as the Informed Consent Forms, Briefing books, Module 2.7 documents, etc.
Khadija Motin
Regulatory Writing Expert Instructor
Khadija has an extensive background in the NHS and completed her undergraduate degree in Radiotherapy and Oncology. She began her career in medical writing as a Medical Writer in QC for a top 10 pharmaceutical company, where she developed a meticulous eye for detail and a strong understanding of regulatory and scientific standards
She now supports PharmaLink as a Medical Editor, applying her clinical knowledge and editorial expertise to deliver high-quality medical communications.
Katie Turner
Regulatory Writing Expert Instructor
Katie Turner is one of our Regulatory Medical Writers who supports students through assignment review and support. She completed a BSc in Biomedical Science at the University of Hull, before undertaking an MSc in Physician Associate Studies at Hull York Medical School.
Katie has worked within the pharmaceutical industry as both a QC editor and Regulatory Medical Writer, gaining experience across a range of regulatory documents including CSRs, protocols, Module 2.7 documents and Investigator’s Brochures. Her experience spans multiple therapeutic areas including oncology and pain management.
Pankti Shah
Medical Writer & PV Expert Instructor
As a Doctor of Pharmacy (PharmD), she brings over seven years of experience in regulatory medical writing, pharmacovigilance, and healthcare article writing, underpinned by a strong academic grounding in pharmacology, therapeutics, and pathophysiology.
She has authored and reviewed a wide range of regulatory documents across the clinical development landscape, including CSRs, CTD modules, IBs, regulatory responses, and bioequivalence reports. Her work covers the full document lifecycle, ensuring data consistency and compliance with global regulatory guidelines.
Her pharmacovigilance expertise spans PSURs, PADERs, RMPs, signal detection, and ICSR processing and submission, making her equally adept at the operational and scientific demands of drug safety.
Lifeter Yenwo-Molo
PV Expert Instructor
Our PV Expert trainer is a seasoned Pharmacovigilance professional with over 12 years of end-to-end experience across aggregate reporting (PSUR, DSUR, RMP, PADER, HA requests), signal management, literature review, ICSR processing, and automation initiatives. With a postgraduate degree in Clinical Research, our expert trainer has successfully led diverse teams, driven process improvements, and delivered high-quality safety outputs. Our PV expert trainer is passionate about knowledge-sharing, people development, and advancing excellence in pharmacovigilance practices.
Sohit Mangla
PV Expert Instructor
Our PV Expert Trainer is an accomplished Pharmacovigilance (PV) professional with over 13 years of comprehensive, end-to-end industry experience. With deep expertise in ICSR management, aggregate reporting (PSURs, DSURs, PADERs), signal management, RMPs, literature review, health authority submissions, database management, and PV systems, he brings valuable real-world insights across the entire drug safety lifecycle.
Divya Priya
Quality and SOP Implementation Lead
Highly Motivated Pharmaceutical professional with over 6 years' experience in Quality Assurance, Overseeing Pharmaceutical Quality Management system. Possess Practical Knowledge of cGMP and Regulatory compliances. Demonstrates a proven track record in developing, managing, and executing Quality Assurance activities and Process improvements. Hands on experience in SOP management, Document control, CAPA, Change control , Risk assessment, and Deviation management. Dedicated in providing strong contribution towards the Organizational goals.
Rabia Abbas
Operations And Programme Delivery Lead
Rabia Abbas is the Operations And Programme Delivery Lead at PharmaLink Academy, bringing over a decade of experience in business operations, administrative management, and HR support. Since 2014, she has helped businesses optimize workflows, streamline HR functions, and strengthen organizational structures. At PharmaLink, Rabia works closely with trainers and participants to ensure a structured and engaging learning experience. Passionate about efficiency and growth, she is committed to building systems that support learners and organizations in achieving long-term success.
Omozuwa Collins
Student Experience Officer
Omozuwa is a medical doctor with a Master’s in Public Health and a strong background in client relations. Having first joined Pharmlink Academy as a student, she experienced firsthand the impact of our programs. Inspired by her journey, she now works with the team to ensure every student feels supported, engaged, and empowered throughout their learning experience.
Voke Agambi
CV Optimization Expert | Social Media Strategist | Talent Acquisition
At PharmaLink Academy, Voke Agambi leads efforts in CV optimization to unlock career opportunities for students in the pharmaceutical sector. She also leads the academy’s social media strategy, building the brand’s online presence and engagement across all platforms, while supporting talent acquisition to strengthen the team.
Imoleoluwa Akinsanya
Executive Assistant
Imoleoluwa is the Executive Assistant to the CEO at PharmaLink, bringing strong expertise in executive support and organizational management. She ensures seamless communication, smooth operations, and effective alignment between leadership and teams. At PharmaLink, Imoleoluwa works closely with the CEO to manage priorities, oversee key initiatives, and maintain excellence across executive functions. Dedicated to precision and professionalism, she is committed to supporting leadership that drives sustainable growth and impact.
Bethan Roe
Medical Editor
Bethan Roe is an experienced Medical Editor with eight years of expertise in the medical research and pharmaceutical education sectors. Coming from a language background, she brings a sharp eye for detail and a passion for clear, effective communication. Bethan is highly proficient in Microsoft Word and is known for her meticulous attention to detail and commitment to editorial excellence. Outside of work, she enjoys exploring new places and discovering new cuisines, as well as reading, writing, and hiking.
Looking Ahead
PharmaLink Academy continues to expand its role as a workforce capability partner supporting professionals and organisations navigating the evolving pharmaceutical landscape.
As global healthcare systems increasingly prioritise regulatory excellence and safety governance, PharmaLink remains focused on developing professionals prepared to contribute meaningfully within these environments.
Explore Capability Pathways
Discover how PharmaLink Academy supports professionals transitioning into pharmaceutical environments through structured, industry‑aligned capability development.