Allucent

Sr. Clinical Project Manager (Europe)

🇬🇧 Bracknell, Reino Unido Híbrido Salud y ciencia Senior Publicado May 22, 2026
Modalidad Híbrido
Seniority Senior
Categoría Salud y ciencia
Idioma English
Publicado 22 de mayo de 2026
Última verificación 27 de mayo de 2026
Contexto de JobGrid

Resumen del puesto por JobGrid

Sr. Clinical Project Manager (Europe) at Allucent: Bracknell, Reino Unido; Híbrido; Senior; Salud y ciencia. JobGrid adds normalized role facts, source context, and a path to the employer application page so candidates can compare the listing before applying.

  • Location and workplace: Bracknell, Reino Unido, Híbrido
  • Role classification: Salud y ciencia, Senior
  • Source freshness: checked by JobGrid on 2026-05-27.
  • Application path: candidates continue to the employer application page with non-personal referral tags.

At Allucent™, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe.

We are looking for a Sr. Project Manager (Sr. PM) to join our A-team (hybrid*/remote). As a Sr. PM at Allucent, you are responsible for the overall coordination and management of clinical trials from start up through to final delivery. The trials are mainly in Oncology, Neuroscience or Immunology and Infectious Diseases. Experience in Cell and Gene Therapy is a plus. This position directs the technical and operational aspects of clinical projects - all with the sense of urgency expected of Allucent customers.

In this role your key tasks will include:

  • Leads the project team, ensuring the project is delivered according to planned scope and timelines in accordance with the contract
  • Creates and executes project management plans required for project delivery and in accordance with established processes
  • Ensures quality and adherence to the relevant policies, SOPs, and working instructions, GCP and regulatory guidelines.
  • Establishes clear communication lines and escalation pathways, communicates with project stakeholders
  • Provides input on study related documents such as the study protocol, CRF, Medical Review/Monitoring plan, and Clinical Study Report
  • Establishes requirements for and ensures project specific training plan for team activities
  • Leads internal and external meetings, with internal and sponsor teams, including Kick Off Meetings (KOM) and Investigator Meetings based on project scope
  • Provides support for vendor identification, qualification and selection and manage vendors
  • Manages vendors and vendor relationships as required for project delivery
  • Ensures effective and efficient resource utilization across projects and programs
  • Produces, maintains and circulates project progress and status reports
  • Manages the study budget, including monthly invoicing.
  • Establishes project risk management plan with input from client and functional stakeholders and oversees adherence and updates throughout the project lifecycle
  • Proactively recognizes and addresses any changes in scope
  • Negotiates and influences internal and external team members in a professional manner and with successful outcomes
  • Effectively solves problems with projects teams by applying strategic thinking and conflict resolution skills
  • Ensures the Trial Master File is kept up to date and inspection ready
  • Serves as the primary point of communication between the sponsor and project team
  • Leads by example and encourages team members to develop strong solutions for clinical trial delivery
  • Responsible for oversight of project team delivery and communication with functional managers, including performance feedback