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Associate Site Manager with Norwegian language

Aplica ya
Mapa de ubicación: Sofia, Bulgaria Full time R1313931

Descripción del trabajo

Associate Site Manager

Real-World Evidence

Hybrid: EMEA

Join us on our exciting journey!

IQVIA Real-World Evidence (RWE) teams work with clients to help them collect and use real-world data to generate evidence to meet the needs of regulators, payers, providers, and patients.

Our approach is unique in the industry and is defining the way companies develop and apply real-world evidence for healthcare decision making.

We are collaborative, intellectually curious, entrepreneurial, and constantly looking for opportunities to harness the value of real-world evidence in an evolving industry.

Due to continued growth, we are seeking new brave minds to join our award winning and innovative department.

Duties:

  • Complete appropriate therapeutic, protocol and clinical research training to perform job duties.
  • Develop an understanding of how sites are staffed and operate in order to build strong relationships with personnel at assigned sites.
  • Gain experience in study procedures by working with experienced Site Management staff. May also work collaboratively with other functional groups such as Project Management, Regulatory Start-Up (RSU) and Epidemiology.
  • Under close supervision, may perform site selection, start-up/regulatory, initiation, monitoring and close out visits in accordance with contracted scope of work, good clinical practices applicable regulations, SOPs and work instructions.
  • Administer protocol and related study training to assigned sites and establish 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), Site Management Lead (SML) and/or line manager.
  • Manage the progress of assigned studies by documenting 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, essential document collection and filing and other required study documentation.
  • Gain experience with standard IQVIA tools, metrics and reports.

Requirements:

  • Degree or currently enrolled in bachelor's degree program preferably in life science; or equivalent combination of education, training and experience.
  • Excellent written and verbal skills in English and Norwegian language (C1 minimum).
  • Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint.
  • Awareness of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines is preferred.
  • Basic organizational, interpersonal, and problem-solving skills.
  • Strong attention to detail.
  • Working time management skills.
  • Ability to establish and maintain effective working relationships with coworkers, managers and clients and site personnel at assigned sites.

What is in it for you?

  • Global exposure
  • Variety of therapeutic areas
  • Collaborative and supportive team environment
  • Access to cutting-edge in-house technology
  • Excellent career development and progression opportunities
  • Work-Life Balance

JOIN US

  • Embrace your curiosity and grow your career in an exciting environment where development is a priority.
  • Think boldly and disrupt conventional thinking.
  • Enjoy what you do.

Whatever your career goals, we are here to ensure you get there!

IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at https://jobs.iqvia.com

IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at https://jobs.iqvia.com

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