Logo of Huzzle

Home

Matches

Explore

Manage

Clinical Research Associate Internship - Paris based

image

IQVIA

2mo ago

  • Internship
    Full-time
    Off-cycle Internship
  • Research & Development
    Healthcare
  • Paris

AI generated summary

  • You should have a scientific or healthcare degree, prior clinical experience preferred, strong computer skills, good communication, organizational abilities, and knowledge of GCP and ICH guidelines.
  • You will assist in site monitoring, training, and communication; evaluate study practices; track study progress; maintain documentation; and support project recruitment efforts.

Requirements

  • Bachelor’s degree in scientific discipline or health care preferred.
  • Equivalent combination of education, training and experience may be accepted in lieu of degree.
  • Prior clinical experience preferred.
  • Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint.
  • Written and verbal communication skills including good command of English language.
  • Organizational and problem-solving skills.
  • Effective time and financial management skills.
  • Ability to establish and maintain effective working relationships with co-workers, managers and clients.
  • Knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.

Responsibilities

  • Complete appropriate therapeutic, protocol and clinical research training to perform job duties.
  • Gain experience in study procedures by working with experienced clinical staff.
  • Under close supervision, perform site monitoring visits (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 as appropriate.
  • Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrolment, Case Report Form (CRF) completion and submission, and data query generation and resolution.
  • Under close supervision, ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with Good Clinical Practice (GCP) / International Conference on Harmonization (ICH) and local regulatory requirements.
  • Under close supervision may support start-up phase.
  • 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.
  • Collaborate and liaise with study team members for project execution support as appropriate.
  • If applicable, learn key facets for successful development of project subject recruitment plan on a per site basis. Suggest ideas for improving site recruitment plan in line with project needs to enhance predictability. Assist in tracking subject site recruitment progress.

FAQs

What is the duration of the CRA Internship?

The CRA Internship is a full-time position with a duration of 6 months.

Where is the CRA Internship based?

The CRA Internship is office-based in the IQVIA office located in Paris.

What qualifications are required for the CRA Internship?

A Bachelor’s degree in a scientific discipline or health care is preferred, but an equivalent combination of education, training, and experience may also be accepted.

Is prior clinical experience necessary for this internship?

Prior clinical experience is preferred but not explicitly required.

What skills are necessary for applicants applying for this position?

Applicants should have proficiency in Microsoft Word, Excel, and PowerPoint, along with strong written and verbal communication skills, organizational and problem-solving skills, effective time management, and the ability to maintain effective working relationships.

Will there be training provided during the internship?

Yes, the internship includes a structured training program to gain knowledge and skills required to conduct clinical monitoring visits.

Are there opportunities for career advancement after completing the internship?

While the internship is a stepping stone, successful completion may lead to potential career opportunities within IQVIA, depending on performance and available positions.

Is a driver's license required for the internship?

The job description does not specify a requirement for a driver's license.

What are the main responsibilities of the CRA Intern?

Responsibilities include conducting site monitoring visits, administering protocol training at sites, evaluating study site practices, managing study progress, and maintaining documentation related to site management.

What is the company culture at IQVIA?

IQVIA fosters a collaborative work environment focused on innovation, integrity, and the advancement of health outcomes, aiming to create intelligent connections in the life sciences and healthcare industries.

image

IQVIA

Accelerate innovation for a healthier world.

Science & Healthcare
Industry
10,001+
Employees

Mission & Purpose

IQVIA (NYSE:IQV) is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. IQVIA creates intelligent connections across all aspects of healthcare through its analytics, transformative technology, big data resources and extensive domain expertise. IQVIA Connected Intelligence™ delivers powerful insights with speed and agility — enabling customers to accelerate the clinical development and commercialization of innovative medical treatments that improve healthcare outcomes for patients. With approximately 86,000 employees, IQVIA conducts operations in more than 100 countries. IQVIA is a global leader in protecting individual patient privacy. The company uses a wide variety of privacy-enhancing technologies and safeguards to protect individual privacy while generating and analyzing information on a scale that helps healthcare stakeholders identify disease patterns and correlate with the precise treatment path and therapy needed for better outcomes. IQVIA’s insights and execution capabilities help biotech, medical device and pharmaceutical companies, medical researchers, government agencies, payers and other healthcare stakeholders tap into a deeper understanding of diseases, human behaviors and scientific advances, in an effort to advance their path toward cures.

Benefits

  • Medical, dental and vision coverage

  • Employee Assistance Programs

  • Mental health support

  • Flexible work environment

  • Time off for leisure, personal time and corporate holidays

  • Parental leave for birth or adoption

  • Paid leave for other life matters (i.e., illness, bereavement, jury duty, military service, etc.)

  • Retirement and savings plans

  • Commuter benefits

Article & News