Senior Clinical Trials Site Activation Lead

PAREXEL INTERNATIONAL (SINGAPORE) PTE. LTD.

Singapore

On-site

SGD 120,000 - 180,000

Full time

3 days ago
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Job summary

PAREXEL INTERNATIONAL (SINGAPORE) PTE. LTD. is seeking a Site Activation Leader to drive planning and strategy for assigned clinical studies, oversee milestones from feasibility to last site activation, and monitor progress to ensure timely and quality study start-up.

You will lead cross‑functional teams, manage risks, report on activation status, and maintain CTMS/EDC/IXRS/TMF documentation. The role includes client relationship management, coordination with project management and site start-up

Qualifications

  • . 4–7 years of experience in clinical research operations with site activation leadership.
  • Proven ability to lead site activation teams and manage complex regulatory start-up requirements.
  • Strong knowledge of regulatory compliance in clinical research.
  • Experience with CTMS, EDC, IXRS, TMF systems.

Responsibilities

  • Lead site activation planning and strategy development for assigned clinical studies.
  • Oversee activation milestones and deliverables to ensure timely and quality study start-up.
  • Monitor and report activation progress across multiple studies and mitigate potential delays or risks.
  • Lead cross-functional teams to resolve complex site activation challenges.
  • Develop, coordinate, and execute the study critical path plan including Site Feasibility, Site Selection, Regulatory Green Light, Site Initiation, and Site Activation, plus related Systems and TMF/EDL responsibilities.

Skills

Project planning
Regulatory knowledge
Stakeholder management
Cross-functional leadership
Communication with senior stakeholders
Change management
Client relationship management

Education

Bachelor's degree in Life Sciences, Healthcare, or related field
Advanced operations or project management training

Tools

CTMS
EDC
IXRS
TMF

Job description

PAREXEL INTERNATIONAL (SINGAPORE) PTE. LTD. is seeking a Site Activation Leader to drive planning and strategy for assigned clinical studies, oversee milestones from feasibility to last site activation, and monitor progress to ensure timely and quality study start-up.

You will lead cross‑functional teams, manage risks, report on activation status, and maintain CTMS/EDC/IXRS/TMF documentation. The role includes client relationship management, coordination with project management and site start-up

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