• Clinical Trials Assitant Jobs in Mexico - 25367637

  • Iqvia
  • Mexico
  • Save Job
  • 1 - 4 Years
  • Posted : above 1 month

Job Description:

Join us on our exciting journey! IQVIA is The Human Data Science Company, focused on using data and science to help healthcare clients find better solutions for their patients Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics and human ingenuity to drive healthcare forward

PURPOSE

Provide administrative support to clinical projects under direction of line manager and/or other designated clinical team members Assists with general administrative functions as required

RESPONSIBILITIES

Assist Clinical Research Associates (CRAs)/In-house Clinical Research Associate (iCRA) and Regulatory and Start-Up (RSU) with accurately updating and maintaining clinical systems that track site compliance and performance within project timelines

Assist the clinical team in the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures Assist with periodic review of study files for completeness

Assist CRAs/iCRAs and RSU with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information

Assist with the tracking and management of Case Report Forms (CRFs), queries and clinical data flow

Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation

May accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training and with required approval

May perform assigned administrative tasks to support team members with clinical trial execution

All responsibilities are essential to job functions unless noted as non-essential (N)

REQUIRED KNOWLEDGE, SKILLS AND ABILITIES

Awareness of applicable clinical research regulatory requirements; ie, Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines

Knowledge of applicable protocol requirements as provided in company training

Computer skills including working knowledge of Microsoft Word, Excel and PowerPoint

Good written and verbal communication skills including good command of English language

Effective time management and organizational skills

Ability to establish and maintain effective working relationships with coworkers, managers and clients

MINIMUM REQUIRED EDUCATION AND EXPERIENCE

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

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