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Job Description
Skill required: Pharmacovigilance Operations - Pharmacovigilance & Drug Safety Surveillance
Designation: Pharmacovigilance Services Specialist
Qualifications:Bachelor of Aryurvedic Medicine And Surgery/Bachelor Degree in Life Sciences/Master Degree in Life Sciences
Years of Experience:7 to 11 years
About Accenture
Accenture is a global professional services company with leading capabilities in digital, cloud and security.Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Song— all powered by the world’s largest network of Advanced Technology and Intelligent Operations centers. Our 699,000 people deliver on the promise of technology and human ingenuity every day, serving clients in more than 120 countries. We embrace the power of change to create value and shared success for our clients, people, shareholders, partners and communities.Visit us at www.accenture.com
What would you do? Oversee and ensure adherence to Quality Management Framework procedures that is required in delivering high quality cases and managing the team’s performance
What are we looking for? Educational and Experience Requirements: • Bachelors in Life Science, Pharmacy, or a Medical Degree • 4-5 years of experience in Pharmacovigilance • Specific experience of QA / auditing of any Pharma domains like Pharmacovigilance, • Clinical Operations, Medical writing, SAS, etc. is desired • Must have the ability to report facts with high degree of accuracy and attention on to detail. • General understanding of ICH, GCP, FDA, MHRA and similar requirements with respect to Clinical Trial and Quality Assurance experience will be desired. • Good verbal and written communication skills desired. • Must have skills of Microsoft office tools like excel, word and power point etc. • Must be able to develop strong interpersonal skills within the team
Roles and Responsibilities: • Implementation of Quality assurance program for PV Engagements. • Establish quality and compliance activities during transition of new deals. • Support in client, due diligence visits/audits and inspections by regulatory authorities • Support in SOP development and maintenance for the assigned project • Ensure data security / privacy measures are implemented in deal teams, by the delivery leads and deal representatives • Compliance oversight for the assigned project. • Attend governance meetings and provide quality updates • Support in deviation review and development of CAPA meeting the requirements. • Follow up on closure of CAPA • Closely monitor the contract updates and the changes required in the processes. • Focus on the standardisation of the process across the locations of an assigned project • Ensure compliance with applicable regulations and deal guidelines including those that are brought to light subsequent to an audit • Serve as a resource for training and answering questions on applicable regulations and deal /client guidelines as applicable • Serve as point of contact for audits and audit follow-up • Inspection readiness • Develop Quality Management Plan for PV deal in compliance with the contract for • Accenture if required • Co-ordination of regulatory Audits in Various deals. • Additional responsibilities as and when required by the managementBachelor of Aryurvedic Medicine And Surgery,Bachelor Degree in Life Sciences,Master Degree in Life Sciences
Designation: Pharmacovigilance Services Specialist
Qualifications:Bachelor of Aryurvedic Medicine And Surgery/Bachelor Degree in Life Sciences/Master Degree in Life Sciences
Years of Experience:7 to 11 years
About Accenture
Accenture is a global professional services company with leading capabilities in digital, cloud and security.Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Song— all powered by the world’s largest network of Advanced Technology and Intelligent Operations centers. Our 699,000 people deliver on the promise of technology and human ingenuity every day, serving clients in more than 120 countries. We embrace the power of change to create value and shared success for our clients, people, shareholders, partners and communities.Visit us at www.accenture.com
What would you do? Oversee and ensure adherence to Quality Management Framework procedures that is required in delivering high quality cases and managing the team’s performance
What are we looking for? Educational and Experience Requirements: • Bachelors in Life Science, Pharmacy, or a Medical Degree • 4-5 years of experience in Pharmacovigilance • Specific experience of QA / auditing of any Pharma domains like Pharmacovigilance, • Clinical Operations, Medical writing, SAS, etc. is desired • Must have the ability to report facts with high degree of accuracy and attention on to detail. • General understanding of ICH, GCP, FDA, MHRA and similar requirements with respect to Clinical Trial and Quality Assurance experience will be desired. • Good verbal and written communication skills desired. • Must have skills of Microsoft office tools like excel, word and power point etc. • Must be able to develop strong interpersonal skills within the team
Roles and Responsibilities: • Implementation of Quality assurance program for PV Engagements. • Establish quality and compliance activities during transition of new deals. • Support in client, due diligence visits/audits and inspections by regulatory authorities • Support in SOP development and maintenance for the assigned project • Ensure data security / privacy measures are implemented in deal teams, by the delivery leads and deal representatives • Compliance oversight for the assigned project. • Attend governance meetings and provide quality updates • Support in deviation review and development of CAPA meeting the requirements. • Follow up on closure of CAPA • Closely monitor the contract updates and the changes required in the processes. • Focus on the standardisation of the process across the locations of an assigned project • Ensure compliance with applicable regulations and deal guidelines including those that are brought to light subsequent to an audit • Serve as a resource for training and answering questions on applicable regulations and deal /client guidelines as applicable • Serve as point of contact for audits and audit follow-up • Inspection readiness • Develop Quality Management Plan for PV deal in compliance with the contract for • Accenture if required • Co-ordination of regulatory Audits in Various deals. • Additional responsibilities as and when required by the managementBachelor of Aryurvedic Medicine And Surgery,Bachelor Degree in Life Sciences,Master Degree in Life Sciences
About Accenture
Accenture is a leading global professional services company that helps the world’s leading businesses, governments and other organizations build their digital core, optimize their operations, accelerate revenue growth and enhance citizen services—creating tangible value at speed and scale. We are a talent- and innovation-led company with approximately 791,000 people serving clients in more than 120 countries. Technology is at the core of change today, and we are one of the world’s leaders in helping drive that change, with strong ecosystem relationships. We combine our strength in technology and leadership in cloud, data and AI with unmatched industry experience, functional expertise and global delivery capability. Our broad range of services, solutions and assets across Strategy & Consulting, Technology, Operations, Industry X and Song, together with our culture of shared success and commitment to creating 360° value, enable us to help our clients reinvent and build trusted, lasting relationships. We measure our success by the 360° value we create for our clients, each other, our shareholders, partners and communities.Visit us at www.accenture.com
Equal Employment Opportunity Statement
We believe that no one should be discriminated against because of their differences. All employment decisions shall be made without regard to age, race, creed, color, religion, sex, national origin, ancestry, disability status, military veteran status, sexual orientation, gender identity or expression, genetic information, marital status, citizenship status or any other basis as protected by applicable law. Our rich diversity makes us more innovative, more competitive, and more creative, which helps us better serve our clients and our communities.