Clinical Trials Manager - Virology

CTM1022024_1706890841
  • £50 - £60 per hour
  • Hayes, London
  • Contract

Job Title: Clinical Trials Manager - Virology

Work Structure: Monday - Friday, 37 hours/week. REMOTE

Pay rate: Up to £60/hour

Contract Length: 12 months

Contract type: INSIDE IR35

Location: Hayes, London, England

Overview: Join our client's global pharmaceuticals company as a Clinical Trials Manager - Virology! This role involves regional management on Phase Ib-III clinical studies, with a strong emphasis on the EMEA region. The successful candidate will work across several studies, including involvement from study start-up to study close-out activities.

Key Responsibilities for the Clinical Trials Manager - Virology include, but not limited to:

  • Provides regional management of global PIb-III studies managed by Clinical Program Manager
  • Contributes to development of study budget.
  • Contributes to development of RFPs and participates in selection of CROs/vendors.
  • Manages CROs/vendors.
  • Serve as the primary point of contact for CROs, addressing questions and applying knowledge to resolve problems.
  • Interacts with cross-functional teams internally and externally to ensure trial progress

Qualifications & Experience:

  • Significant relevant experience and a BSc or nursing qualification in a relevant scientific discipline
  • Previous experience in Virology areas would be advantageous but not essential.
  • Must have previous study management/coordination experience at Sr CTMA level.
  • Monitoring experience is highly desirable as co-monitoring will be required.
  • Thorough knowledge and understanding of FDA and EU Regulations, ICH Guidelines, and GCPs governing the conduct of clinical trials is desirable.

Knowledge & Skills:

  • Must be able to generally understand, interpret, and explain protocol requirements to others.
  • Must be able to prioritise multiple tasks.
  • Must be able to participate in multiple departmental or interdepartmental strategic initiatives under limited supervision.
  • Must have a general, functional expertise to support SOP development and implementation.
  • Must be able to resolve problems using national and international regulations, guidelines, and investigator interaction.
  • Excellent teamwork, decision-making and organisational skills are key to success.
  • Strong communication skills

Does this sound like you? If so, please apply today!

Get in touch to discuss this role!

My number is 020 7 551 0727

jkirlew@i-pharmconsulting.com

Jada Kirlew Senior MSP Consultant

Apply for this role