Vice President Resume Template

Bridgemont, UK • [email protected] • +44 203 993 4860
Results-oriented VP of Regulatory Affairs with a 15+ year track record of enabling clinical, CMC, and non-clinical development, with experience in both early- and late-stage product development. Dedicated to building high-performing teams, driving continuous improvement, and ensuring strict compliance with regulatory requirements.
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Biogalenica Therapeutics Ltd. | Bridgemont, UK 12/2020 – Present
VP Head of Regulatory Affairs & Medical Writing
Currently orchestrating all aspects of the Regulatory Affairs function to facilitate nonclinical, clinical, and CMC development of novel antibody-fusion and bispecific antibody products for treatment of ulcerative colitis and severe acute alcoholic hepatitis. Achievements to date include the following:
Genora BioSolutions Ltd. | Remote, UK/Europe 02/2020 – 10/2020
Head of Regulatory Strategy & Science
Provided regulatory leadership for complex clinical and CMC development operations focusing on autologous gene-edited hematopoietic stem cell therapeutics for sickle cell and other diseases. Highlights included the following:
VisceraBio International | London, UK 03/2019 – 01/2020
Executive Director – Regulatory Affairs – Ophthalmology
Managed the Regulatory Affairs function for this global Biosciences organization including in-depth strategic planning, analysis, and interaction with regulatory agencies (FDA). Achievements included:
Nexira Pharma Ltd. | Cambridge & Geneva 05/2014 – 03/2019
Senior Director – Regulatory Affairs, 01/2020 – 03/2020
Director – Regulatory Affairs, 06/2018 – 12/2019
Associate Director – Regulatory Affairs, 07/2015 – 05/2018
Senior Manager – Regulatory Affairs, 05/2014 – 06/2015
Spearheaded the Regulatory Affairs department with accountability for designing and implementing infrastructure and processes to maximize the likelihood of CMC, clinical and nonclinical development regulatory success of different development programs. Hired, trained, and mentored the regulatory and medical writing functional team. Provided expert guidance for senior executives and acted as a critical resource for colleagues on all matters involving regulatory affairs. Progressed to roles of increasing managerial responsibility due to outstanding contributions. Highlights:
Oncorion Therapeutics | Surrey, UK 08/2012 – 05/2014
Manager – Regulatory Affairs, HIV
Delivered regulatory guidance for clinical operations teams during all phases of studies. Accomplishments included:
Regulis Biopharma | Frankfurt, Germany 12/2008 – 07/2012
Senior Regulatory Associate
Enabled late state development activities as regulatory lead and FDA liaison for three investigational drug products (monoclonal antibodies). Highlights included the following:
Scientist, Regulis Biopharma
Postdoctoral Fellow, European Biomedical Research Institute
Postdoctoral Research Associate, University of Lausanne / University of Bergen
PhD in Medicinal Chemistry and Pharmaceutics
University of Edinburgh, College of Pharmacy
Awarded John Bruce Scholarship for Outstanding Graduate Student in Pharmaceutical Sciences
Bachelor of Pharmaceutical Sciences
Mumbai Institute of Chemical Technology (Formerly called University Department of Chemical Technology)
Having a career in pharmaceutical regulatory affairs means balancing science, strategy, and cross-border compliance. Whether you’re eyeing the next VP seat or want to showcase your expertise in clinical, CMC, and global submissions, your resume must be written by professional certified resume writers online and tell a story of both biotechnical mastery and strategic leadership.
Let’s break down the essential steps to building a compelling Regulatory Affairs resume, using insights from the career trajectory of Dr. Anita R. Sharma, PhD, one of the sector’s standout leaders.
Open with your unique value:
Immediately set the tone by summarizing your years of experience, the depth of your regulatory knowledge (clinical, CMC, non-clinical), and your talent for building teams and ensuring compliance in complex, ever-evolving landscapes.
Example: Results-driven VP of Regulatory Affairs with 15+ years enabling product development, compliance, and cross-functional leadership across early- and late-stage programs. Expert at translating scientific discovery into actionable regulatory strategy for successful global submissions and approvals.
Section off core skills in a visually distinct list. Think:
Tip from biotech resume writers: Don’t shy from including major scientific or biotechnical skills unique to your portfolio (e.g., biosimilars, gene-editing, orphan drugs).
Quantify and contextualize your impact:
For each role, highlight tangible outcomes:
Tip: Focus on the business and scientific value you delivered, not just the tasks you performed.
Show how you’ve been the linchpin:
Highlight your leadership from inception through execution:
For senior candidates, a dedicated section for publications, patents, or speaking engagements can elevate your authority:
Show your ability to navigate international regulations and collaborate with multiple health authorities:
Show career growth through roles of increasing scope, complexity, and authority:
A PhD (or advanced degree) is often a baseline in this field. List:
Modern regulatory leaders are change agents. Include:
By following these steps from Resume Writing Lab’s healthcare executive resume writing service, your CV will reflect the technical depth, regulatory sophistication, and executive leadership needed to lead teams and shape the future of compliance and development in the pharmaceutical industry.