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Risk Management Product Lead

CK Group- Science, Clinical and Technical
Posted a day ago, valid for 19 days
Location

Tadworth, Surrey KT20, England

Salary

£40.93 - £51.97 per hour

Contract type

Full Time

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Sonic Summary

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  • CK Group is seeking a Risk Management Product Lead for a 12-month contract in the Pharmaceutical industry, located in Tadworth.
  • The salary for this position ranges from £40.93 to £51.97 per hour (PAYE) or £45.87 to £58.24 per hour (Umbrella).
  • Candidates must have a minimum of 5 years of progressive experience in the pharmaceutical field, focusing on drug safety risk management.
  • The role involves providing strategic expertise in risk management planning and implementing Risk Management Plans (RMP) to enhance patient safety.
  • Preferred qualifications include a degree in health science, project management certification, and experience in global drug safety risk management activities.
CK Group are recruiting for a Risk Management Product Lead, to join a company in the Pharmaceutical industry, at their site based in Tadworth, on a contract basis for 12 months.


Salary:

40.93 per hourto 51.97 per hour(PAYE) or 45.87 per hourto 58.24 per hour (Umbrella).


Risk Management Product Lead Role:
  • Provides strategic expertise to product teams and will drive the execution of Risk Management (RM) activities included within RMP (Risk Management Plans) across business units to embed a culture of innovative and efficient risk management strategies to enhance patient safety.
  • Provides expertise regarding RMP requirements and implementation for pre-marketed and post-marketed drug products.
  • Recommends appropriate risk mitigation options for drug related safety issues, taking into account the benefit-risk profile of the drug, and approaches used for other products internal and external to the company.
  • Develops/evolves/implements best practices in risk management planning, including risk communication, risk minimization and in benefit/risk assessment methodologies.
  • Supports with strategic guidance for risk management planning, taking into consideration local regulatory requirements, risk management best practices, and product specific risk profile, and development and implementation of RMP initiatives for products within our client's portfolio.
  • Serves as the key interface in matters related to oversight of implementation and tracking of commitments included within the RMP and provide periodic updates regarding the status of implementation.

Your Background:
  • Experience in participating in audits and experience with inspection readiness.
  • Minimum 5 years of broad and progressive pharma experience in medical, clinical or pharmacovigilance but with a clear focus on drug safety risk management.
  • B.S., M.S. in health science (Pharm.D, or Ph.D preferred).
  • Demonstrated experience in global drug safety risk management planning activities and generating RMP.
  • Project management certification (PMP) and Six Sigma Certification preferred.

Company:

Our client is one of the world's premier innovative biopharmaceutical companies, discovering, developing and providing over 160 different medicines, vaccines and consumer healthcare products to help improve the lives of millions of people in the UK and around the world every year.


Location:

This role is based at our clients site in Tadworth.


Apply:

It is essential that applicants hold entitlement to work in the UK. Please quote job reference (Apply online only) in all correspondence.


Please note:

This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.


If this position isn't suitable but you are looking for a new role, or if you are interested in seeing what opportunities are out there, head over to our LinkedIn page (cka-group) and follow us to see our latest jobs and company news.

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By applying, a CV-Library account will be created for you. CV-Library's Terms & Conditions and Privacy Policy will apply.