• CRA Trainee Jobs in Netherlands - 25367675

  • Iqvia
  • Netherlands
  • Save Job
  • 1 - 3 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

Engage in company training program to gain knowledge and skills required to independently conduct clinical monitoring visits in accordance with study protocol, standard operating procedures, good clinical practice, and applicable regulatory requirements Transition to an independent CRA role after the training period

RESPONSIBILITIES

Complete appropriate therapeutic, protocol and clinical research training to perform job duties
Gain experience in study procedures by working with experienced clinical staff in Clinical Research Associate (CRA), Clinical Research Specialist (CRS) and Clinical Trials Assist (CTA) roles May also work collaboratively with other functional groups such as Data Management and Pharmacovigilance
Under close supervision, perform site selection, initiation, monitoring and close out visits in accordance with contracted scope of work and good clinical practices
Under close supervision, administer protocol and related study training to assigned sites and establishes regular lines of communication with sites to manage ongoing project expectations and issues
Under close supervision, 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 to Clinical Project Manager (CPM), CRS and/or line manager
Under close supervision, 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
Under close supervision, 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

REQUIRED KNOWLEDGE, SKILLS AND ABILITIES

Awareness of applicable clinical research regulatory requirements; ie, Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines Any clinical research related experience/practice is an advantage
Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer
Good written and verbal communication skills including good command of English and Dutch languages
Basic organizational and problem-solving skills
Working time management skills
Ability to establish and maintain effective working relationships with coworkers, managers and clients

MINIMUM REQUIRED EDUCATION AND EXPERIENCE

Degree or currently enrolled in bachelors degree program in health care or other related discipline; or equivalent combination of education, training and experience PhD / post-doc is preferred

We know that meaningful results require not only the right approach but also the right people Regardless of your role, we invite you to reimagine healthcare with us You will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve human health outcomes Whatever your career goals, we are here to ensure you get there! We invite you to join IQVIA

Job ID R1055619

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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