• 16254- CRA 1 Jobs in Chile - 25368584

  • Iqvia
  • Chile
  • Save Job
  • 2 - 3 Years
  • Posted : above 1 month

Job Description:

IQVIA is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward

Perform site selection (if applicable), initiation, monitoring and close-out visits in accordance with contracted scope of work and good clinical practice If applicable, Senior Clinical Research Associates may be accountable for development of project subject recruitment plan on a per site basis Work with sites to adapt, drive and track subject recruitment plan in line with project needs to enhance predictability
RESPONSIBILITIES
Perform site selection (if applicable), initiation, monitoring and close-out visits in accordance with contracted scope of work and good clinical practice
If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis Work with sites to adapt, drive and track subject recruitment plan in line with project needs to enhance predictability
Provide monitoring visits and site management for a variety of protocols, sites and therapeutic areas
Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues
Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations Escalate quality issues as appropriate
Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution May support start-up phase
Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation
Act as a mentor for clinical staff including conducting co-monitoring and training visits
May provide assistance with design of study tools, documents and processes
Convey features and opportunities of study to site
Collaborate and liaise with study team members for project execution support as appropriate

Join Us

Making a positive impact on human health takes insight, curiosity, and intellectual courage It takes brave minds, pushing the boundaries to transform healthcare Regardless of your role, you will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve outcomes for patients

Forge a career with greater purpose, make an impact, and never stop learning

Job ID R1102043

Profile Summary:

Employment Type : Full Time
Eligibility : Any Graduate
Industry : Consulting Services
Functional Area : Bio Tech/R&D/Scientist
Role : Clinical Research
Salary : As per Industry Standards
Deadline : 09th Jun 2020

Key Skills:

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