Nadia Mohan BPharm MRPharmS
Bletchley, Milton Keynes
Summary
PERSONAL PROFILE Over 18 years of dedicated experience in the pharmaceutical and healthcare industry. Proficient in problem identification and resolution, demonstrating keen attention to detail. Expertise in adhering to GCP, GMP, and GLP guidelines, ensuring top-tier quality standards. Comprehensive understanding of global pharmacovigilance regulations and compliance. Exceptional skills in organization, interpersonal relations, communication, and fostering collaboration.
Overview
15
15
years of professional experience
Work History
Senior Drug Safety Scientist
Sanofi Aventis
Maidenhead
07.2017 - 11.2019
- Led the pharmacovigilance team, ensuring efficient case management and regulatory compliance
- Developed and executed proactive pharmacovigilance strategies, improving safety outcomes
- Managed regulatory inspections and audits, maintaining compliance with standards
- Oversaw safety signal detection and assessment processes
- Collaborated with regulatory authorities for timely submissions
- Implemented training programs for staff development
- Enhanced data analysis techniques for robust safety assessments
- Integrated safety insights into early product development
- Contributed to a strong reputation for safety and compliance in the industry.
Senior PV Officer
Sanofi Pasteur MSD
Guildford
10.2016 - 04.2017
- Managed safety case processing and contributed to periodic safety reports
- Collaborated with cross-functional teams to ensure compliance with pharmacovigilance regulations
- Enhanced safety monitoring strategies to streamline processes
- Played a key role in risk assessment and management of adverse events
- Conducted in-depth analysis of complex safety data.
Drug Safety Associate
Johnson & Johnson
High Wycombe
10.2009 - 09.2016
- Led triage and prioritization of incoming cases for daily workflow
- Oversee processing and quality review of cases in Argus database, including narrative summaries
- Collaborated with medical assessment physicians to resolve ambiguities
- Contributed to periodic reports, such as IND and PSUR
- Developed procedural documents and reviewed protocols for oncology products
- Led the Johnson & Johnson Credo Task Force
- Acted as the primary point of contact for global safety case exchange
- Mentored and trained new staff in case handling activities.
Clinical Trial Supplies Technician
Allergan Pharmaceuticals
04.2008 - 09.2009
- Key member of the clinical supplies team, working closely with the team leader
- Managed bulk drug supply orders and assembled investigational supplies for shipment
- Shipped clinical supplies to investigative sites
- Applied labels to investigational medications per instructions
- Ensured compliance with regulations and company policies for adverse event reporting
- Distributed randomization sheets to investigators
- Provided training and support to new staff.
Pharmacy Technician
Vantage Pharmacy
St. Peters
09.2006 - 03.2008
- Collaborated closely with pharmacists to ensure strict adherence to all regulatory practices, guidelines, and quality standards
- Managed medication orders efficiently, optimizing inventory control and contributing to streamlined supply chain operations
- Demonstrated precision in accurately inputting prescription orders into the computer system, resulting in a seamless workflow and enhanced patient care
- Assisted in patient consultations and medication counseling, ensuring clarity and compliance with medication instructions
- Actively participated in continuous training and professional development to stay updated with the latest pharmaceutical advances and best practices.
Production Pharmacist
Wyeth Pharmaceuticals
07.2004 - 07.2006
- Formulated pharmaceutical products to ensure stability and safety
- Maintained strict quality control standards and upheld regulatory compliance
- Oversaw production processes to optimize efficiency and resolve issues
- Documented batch records meticulously to ensure regulatory adherence
- Managed equipment and facility operations to guarantee quality assurance
- Collaborated on initiatives for continuous process improvement and enhanced safety measures.
Education
Medical Aspect of Adverse Drug Reactions -
DSRU Education and Research Limited
2011
CRA Certification from the - undefined
Clinical Research Training Institute
2008
Bachelors - Pharmacy
University of Karachi
2004
undefined
Sir Syed Girls College
1999
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St. John's High School
1997
Skills
- Patient safety compliance
- Documentation abilities
- Quality Assurance
- Process improvement
- Regulatory requirements
Interests
I derive enjoyment from a diverse range of activities, including:
Chess: Strategizing and challenging my mind through the game of chess.
Travel Adventurer: Discovering new travel destinations, cultures, and cuisines to broaden my horizons.
Creative Expression: Nurturing my creativity through song writing, a passion that has led to my recognition as a Spotify Verified Artist.
These interests not only provide personal fulfilment but also contribute to my well-rounded perspective, enriching both my personal and professional growth.
Languages
English
Advanced
Hindi
Advanced
Urdu
Advanced
Timeline
Senior Drug Safety Scientist
Sanofi Aventis
07.2017 - 11.2019
Senior PV Officer
Sanofi Pasteur MSD
10.2016 - 04.2017
Drug Safety Associate
Johnson & Johnson
10.2009 - 09.2016
Clinical Trial Supplies Technician
Allergan Pharmaceuticals
04.2008 - 09.2009
Pharmacy Technician
Vantage Pharmacy
09.2006 - 03.2008
Production Pharmacist
Wyeth Pharmaceuticals
07.2004 - 07.2006
Medical Aspect of Adverse Drug Reactions -
DSRU Education and Research Limited
CRA Certification from the - undefined
Clinical Research Training Institute
Bachelors - Pharmacy
University of Karachi
undefined
Sir Syed Girls College
undefined
St. John's High School
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