Senior Clinical Trial Manager - Remote-Driven Impact

Bristol Myers Squibb

Madrid

On-site

EUR 90,000 - 130,000

Full time

2 hours ago
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Job summary

Bristol Myers Squibb in Madrid is seeking a Senior Clinical Trial Manager to oversee studies across their lifecycle, coordinating cross-functional teams and stakeholders to ensure timely, on-budget delivery of trial deliverables.

The role involves monitoring regulatory compliance, CAPAs, CRO and vendor management, site initiation and close-out visits, and risk mitigation, with emphasis on collaboration and quality in a fast-paced environment.

Responsibilities

  • Oversees and collaborates with study team members and cross-functional stakeholders, to proactively identify opportunities and manage and mitigate risks and to ensure timely and on-budget execution of clinical trial deliverables.
  • Supports internal audit and inspection activities and contributes to corrective and preventive actions (CAPAs), including leading the resolution of issues when appropriate.
  • Monitors updates throughout a study’s lifecycle for compliance with regulations and SOPs, including CRA compliance with study parameters and tracks escalation and closure of action items noted in monitoring visit reports during late phase studies including registration of protocols.
  • Monitors progress of clinical trials and identifies and resolves any issues or risks that may impact timelines or study outcomes.
  • Serves as the key operational contact for clinical studies, providing oversight for the site evaluation, initiation and close-out visits in addition to routine monitoring visits.
  • Participates in CRO and vendor selection and manages all interactions and deliverables from relevant CROs and vendors under the guidance of leadership.

Job description

Bristol Myers Squibb in Madrid is seeking a Senior Clinical Trial Manager to oversee studies across their lifecycle, coordinating cross-functional teams and stakeholders to ensure timely, on-budget delivery of trial deliverables.

The role involves monitoring regulatory compliance, CAPAs, CRO and vendor management, site initiation and close-out visits, and risk mitigation, with emphasis on collaboration and quality in a fast-paced environment.

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