Clinical Trial Associate

Clinical Trial Associate

Job Title

Clinical Trial Associate (CTA)

 

Job Status

Full Time

 

Job Summary

The Clinical Trial Associate (CTA) supports at least one primary project, and depending on scope and phase of project, may support multiple projects. The CTA provides support to one or more Clinical Trial Managers (CTM). Interacts with various study support groups and the business unit in order to assist in the development of study plans and project deliverables. The CTA may also be assigned to other non-trial related activities such as process and procedure teams.

 

Job Details

  • Support CTMs in developing study-related documents, which might include study plans, investigator files and informed consent documents
  • Support site selection process by documenting meetings with appropriate departments and individuals and tracking progress by maintaining draft site list
  • Maintains trackers on multiple activities including clinical study timelines and budgets
  • Prepares minutes from team meetings
  • Supports regulatory submissions and communications
  • Works with Study Team to track activities for all milestones
  • Supports good clinical practice (GCP) and regulatory compliance
  • Supports good relations with clinical sites, physicians, medical research staff and outside consultants
  • Supports CTM in other activities, as needed

 

Candidate Requirements (External)

Primary Qualifications:

An undergraduate degree in life sciences

Additional Qualifications:

  • Proficiency with Microsoft Office and use of electronic document templates
  • Time management and project management skills are essential
  • Ability to solve problems, deliver on commitments and work with multidisciplinary teams
  • Independent, self-starting individual with a demonstrated ability to thrive in smaller, biopharma environment is required
  • Strong interpersonal and organizational skills and excellent verbal and written communication skills are required
  • Excellent collaboration skills with strong attention to detail and the ability to multitask and manage complexity
  • Reads, writes and speaks fluent English

 

Send resume and cover letter to angieprice@lskbiopharma.com.