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Clinical Trial s Management Associate I

Parkside Office Professional
Job LocationWest Drayton
EducationNot Mentioned
Salary£167.00 - £180.00 per day
IndustryNot Mentioned
Functional AreaNot Mentioned
Job TypeContract , full-time

Job Description

Exciting opportunity has arisen to join the Late Phase Clinical Operations team based at the International Headquarters in Uxbridge, as a contractor Clinical Trial Management AssociateHybrid workingKey Accountabilitys

  • Serves as the key operational contact with external investigators and internal stakeholders
  • Evaluates scientific proposals or protocols to identify logistical, regulatory and safety elements and implications
  • Manages assigned studies by establishing strong partnerships with external investigators and collaborators to ensure CO and ISR Agreements for financial and company product support are processed in a timely manner and to a high quality
  • Proactively identifies operational challenges and in collaboration with senior team members provides and implements solutions to ensure studies remain on track
  • Maintains efficient collaboration with Clinical Pricing and Finance teams and external investigator/study representative to ensure contracts are executed in a timely manner
  • Supports study drug planning and shipping activities with Clinical Supply Chain Management (CSCM) teams
  • Forecasts, tracks and reports CO and ISR milestones within Clinical Trial Management Systems (CTMS) systems, as well as verifies completeness of the study milestones prior to invoice payment
  • Provides monthly study updates to the appropriate internal stakeholders
  • Implements working processes to promote high quality, efficient, and compliant systems for Late Phase research management
  • Supports and implements Clinical Operations Quality Initiatives
  • Maintains internal Clinical Operations and Medical Affairs databases, tracking systems and clinical study data and document repositories
  • Performs administrative duties in a timely manner as assigned
Knowledge, Skills and Experience* Typically requires a BSc in a relevant scientific discipline and 2+ years of relevant clinical experience in the pharmaceutical or health care industry or equivalent.* Excellent planning, time management, organizational, and administrative skills.* Good knowledge and understanding of ICH GCP, FDA and EMEA regulations* Must be proficient with MS Word, PowerPoint, Outlook, and Excel.* Must be familiar with routine medical/scientific terminology.Parkside Recruitment Ltd is acting as an Employment Business in relation to this vacancy. Parkside Recruitment is an Equal Opportunities Employer.

Keyskills :
Clinical Trials- Late Phase

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