PRA Health Sciences

Senior Associate Study Management


PayCompetitive
LocationRemote
Employment typeOther

This job is now closed

  • Job Description

      Req#: 119219
      Employer Industry: Clinical Research Organization

      Why consider this job opportunity:
      - Opportunity for career advancement and growth within the organization
      - Comprehensive and competitive total reward package, including base pay and variable pay
      - Best-in-class employee benefits tailored to support you and your family
      - Commitment to a continuous learning culture and professional development
      - Inclusive and diverse work environment free of discrimination and harassment
      - Supportive policies and wellbeing initiatives for employees

      What to Expect (Job Responsibilities):
      - Collaborate with clinical trial management staff to support execution and monitoring of clinical studies
      - Participate in study planning, vendor management, and coordination of implementation plans
      - Prepare, write, and review study-related documents, including protocols and consent forms
      - Assist in the identification and evaluation of clinical trial investigators and research units
      - Manage study budgets, timelines, and investigational product arrangements

      What is Required (Qualifications):
      - Working knowledge of ICH, GCP, FDA regulations, and applicable international guidelines
      - Experience with interactions with outside vendors, such as CROs and contract labs
      - A Master's degree or BA/BS/BSc or RN with 3 years of experience in a life sciences field, or an Associate’s degree with 6 years of experience, or a High School diploma with 10 years of experience
      - Strong organization, planning, and communication skills
      - Experience in project planning, oversight of study deliverables, budgets, and timelines

      How to Stand Out (Preferred Qualifications):
      - Experience in developing prospective site-selection criteria
      - Ability to use scientific knowledge to conceptualize study designs
      - Proven experience in anticipating and resolving problems
      - Ability to write and present clearly on scientific and clinical issues
      - Experience leading cross-functional teams in a team/matrix environment

      #ClinicalResearch #CareerAdvancement #EmployeeBenefits #InclusiveWorkplace #ProfessionalDevelopment

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      We are not the EOR (Employer of Record) for this position. Our role in this specific opportunity is to connect outstanding candidates with a top-tier employer.
  • About the company

      We are a global healthcare intelligence partner with everything you need to take your assets from concept to compound to cure.

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