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Drug safety Risk Management

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Cotswold District

On-site

GBP 80,000 - 100,000

4 days ago
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Job summary

An established industry player is seeking a Risk Management Product Lead to enhance patient safety through innovative risk management strategies. In this pivotal role, you will provide strategic expertise, develop best practices, and ensure compliance with regulatory requirements. You will collaborate with product teams to implement effective risk management plans for drug products, making a significant impact on patient safety. This exciting opportunity is perfect for those with a strong background in pharmaceutical risk management and a passion for improving healthcare outcomes.

Qualifications

  • 5+ years of pharma experience focused on drug safety risk management.
  • Experience in audits and inspection readiness is essential.

Responsibilities

  • Drive execution of Risk Management activities across business units.
  • Develop and implement best practices in risk management planning.

Skills

Risk Management

Drug Safety

Pharmacovigilance

Project Management

Inspection Readiness

Education

B.S. in Health Science

M.S. in Health Science

Pharm.D or Ph.D

Tools

Six Sigma Certification

Project Management Certification (PMP)

Job description

Job Description

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 p/h to £51.97 p/h (PAYE) or £45.87 p/h to £58.24 p/h (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).
  • Demonstrated experience in global drug safety risk management planning activities and generating RMP.
  • Project management certification (PMP) and Six Sigma Certification.

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:

For more information, or to apply for this Risk Management Product Lead please contact the Key Accounts Team on 01438 870011 or email pharmacontracts@ckagroup.co.uk. Please quote reference 124 003.

It is essential that applicants hold entitlement to work in the UK.

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

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