Sr. Clinical Trial Assistant / Associate CTM

  • Salary: Competitive
  • REF Number: v-105377
  • Consultant: Anett Racz
  • Contact: +31 23 557 85 29
  • Date Published: 12.07.2024
  • Industry: Other
  • Location: Waltham, United States
  • Functional Expertise: Clinical Operations/Development, Research & Development

CK Group are seeking a highly skilled and motivated Sr. Clinical Trial Assistant or Associate Clinical Trial Manager to join our client based in Waltham. Our client is a clinical stage precision immuno-oncology company. This person will be responsible for the successful planning, implementation and execution of contracted clinical monitoring activities. They will ensure clear client and internal team communication, process documentation, and coordination of relevant work.

 This role is an on site position, full time and on a permanent basis, located in Waltham, MA.

Job Responsibilities

  • Drive the operational planning, content, execution, and delivery for one or more clinical trials.
  • Act as the main point of contact for assigned CRO and translational vendors to ensure GCP compliance and adherence to the scope of work while maintaining budgets and timelines.  Responsible for trial related activities from startup to close-out of a clinical trial in close collaboration with internal stakeholders and CROs.
  • Support trial deliverables both in clinical and translational in a proactive and quality manner
  • Contribute to the development and implementation of study related documents such as protocol amendments, plans, and tracking tools.
  • Foster effective communication and collaboration with internal and external stakeholders, such as investigators, study sites contract research organizations (CROs), and vendors
  • Participate in process improvement and quality-related initiatives associated with study execution and deliverables; participate in establishment of best-in-class processes and standards for study conduct
  • Contribute to a collaborative culture within and outside Clinical Development and actively manage best practice sharing and capability building within the clinical team
 

Qualifications And Education Requirements

  • Bachelor's degree with minimum 3+ years of industry experience
  • Phase I oncology experience
  • Excellent project management skills, particularly, with managing CROs, consultants, and vendors in a team environment
  • Excellent interpersonal skills
 

 

Apply:

It is essential that applicants hold entitlement to work in the US. Please quote job reference 105377 in all correspondence.

 

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