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Clinical Trial Manager

2 hours, 2 minutes ago
Singapore, Australia
Full-time
Senior
Program Manager
Project and Program Management
Apply Now
Precision For Medicine

Precision For Medicine

Precision for Medicine is a specialized scientific services company that helps pharmaceutical and life sciences clients innovate, develop, and commercialize next-generation medical products. With a diverse team of experts, they offer comprehensive serv...

Pharmaceuticals
1K-5K
Founded 2012
$225M raised
View All Jobs 32

Description

  • Serve as the primary clinical point of contact for the client.
  • Lead the planning, conduct, and oversight of the operational portion of clinical studies.
  • Develop clinical study documents, including plans, informed consent templates, study forms, manuals, and training materials.
  • Identify training needs for CRAs and third-party vendors and present materials at investigator meetings and study kick-off meetings.
  • Generate site lists, drive site feasibility, and assess risks to enrollment targets.
  • Develop and finalize country recruitment and retention strategies.
  • Build effective relationships with investigators and study teams to support site start-up, enrollment, maintenance, and closeout.
  • Lead internal clinical team meetings and set expectations for CRAs and CTAs.
  • Oversee submissions and approvals to competent authorities and IRB/ethics committees.
  • Develop monitoring strategies, review metrics, and communicate study issues to project management and clinical staff.
  • Manage eTMF implementation and ongoing trial documentation oversight.
  • Collaborate on CAPAs, GCP audit readiness, data quality, investigational product accountability, and vendor oversight.
  • Step in to assume project management responsibilities when a cross-functional PM is not assigned.
  • Support business development and marketing activities as needed.

Requirements

  • Bachelor’s degree or equivalent education/experience in a science or health-related field; advanced degree preferred.
  • 5–8 years of clinical research experience, with significant clinical monitoring experience.
  • Oncology Phase I trial experience in Australia is preferred.
  • Experience with Microsoft Office products, including Outlook, Word, Excel, and PowerPoint.
  • Excellent communication and interpersonal skills for team-based collaboration.
  • Strong organizational skills, attention to detail, and a customer service-oriented demeanor.
  • Ability to travel domestically and internationally, including overnight stays.
  • Experience with clinical trial systems and reporting tools such as CTMS and eTMF is preferred.
  • Experience managing clinical vendors, site budgets, or investigator contracts is preferred.

Benefits

  • The posting does not specify compensation, equity, or bonus details.
  • The posting does not list health, retirement, or paid time off benefits.
  • Reasonable accommodation support is available for applicants with disabilities.
  • Employment is offered by an Equal Opportunity Employer.
  • A formal interview process is required before any job offer is made.

Interested in this position?

Apply directly on the company website

Apply Now

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