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Site Enrollment and Engagement Lead (m/w/d)

IQVIA

Site Enrollment and Engagement Lead (m/w/d)

full-timePosted: Aug 24, 2026Updated: Sep 1, 2026Germany, Hesse, Frankfurt

Job Description

Join our team as a Site Enrollment and Engagement Lead and play a pivotal role in advancing clinical research. This role collaborates with research staff and stakeholders to drive trial recruitment and deliver study-specific training. Acting as a strategic partner, you will optimize site experience and performance while fostering strong relationships and sharing medical and scientific information with healthcare providers and caregivers.Key ResponsibilitiesDevelop study-specific action plans with research sites to accelerate recruitment and support procedural training.Educate healthcare professionals and their staff on study protocols related to clinical trials.Partner with referral networks to identify potential trial participants.Maintain and analyze customer records to tailor strategies for pre-screening, screening, and enrollment.Complete internal reporting and organize group events to optimize program delivery.Address and manage objections effectively.Stay current with technical knowledge in relevant therapeutic areas.QualificationsBachelor's Degree (BA/BS) in Health Sciences or related field, or equivalent academic/professional qualificationsClinical research experience at the site level requiredNurse or other healthcare professional preferredCRA experience preferredHigh flexibility to travel (including internationally if needed).Located in Germany with fluency in German and English languages.Clinical competence in the therapeutic area.Excellent interpersonal and communication skills.Strong written and verbal communication skills.Ability to work independently and coordinate across multiple functions.Solutions-oriented approach and positive attitude.Strong customer service orientation and collaborative mindset.Demonstrates empathy and cultural awareness.Upholds the values of IQVIA.Why Join Us?At IQVIA, we are committed to improving patient outcomes through innovation and collaboration. As a Site Enrollment and Engagement Lead you will make a meaningful impact on clinical research and contribute to advancing healthcare globally.IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.comIQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Locations

  • Germany, Hesse, Frankfurt

Skills Required

  • Germanintermediate

Required Qualifications

  • Bachelor's Degree (BA/BS) in Health Sciences or related field, or equivalent academic/professional qualifications (degree in health sciences or related field)
  • Clinical research experience at the site level required (experience)
  • Nurse or other healthcare professional preferred (experience)
  • CRA experience preferred (experience)
  • High flexibility to travel (including internationally if needed). (experience)
  • Located in Germany with fluency in German and English languages. (experience)
  • Clinical competence in the therapeutic area. (experience)
  • Excellent interpersonal and communication skills. (experience)
  • Strong written and verbal communication skills. (experience)
  • Ability to work independently and coordinate across multiple functions. (experience)
  • Solutions-oriented approach and positive attitude. (experience)
  • Strong customer service orientation and collaborative mindset. (experience)
  • Demonstrates empathy and cultural awareness. (experience)
  • Upholds the values of IQVIA. (experience)
  • Bachelor's Degree (BA/BS) in Health Sciences or related field, or equivalent academic/professional qualifications (degree in health sciences or related field)

Preferred Qualifications

  • High flexibility to travel (including internationally if needed). (experience)
  • Located in Germany with fluency in German and English languages. (experience)
  • Clinical competence in the therapeutic area. (experience)
  • Excellent interpersonal and communication skills. (experience)
  • Strong written and verbal communication skills. (experience)
  • Ability to work independently and coordinate across multiple functions. (experience)
  • Solutions-oriented approach and positive attitude. (experience)
  • Strong customer service orientation and collaborative mindset. (experience)
  • Demonstrates empathy and cultural awareness. (experience)
  • Upholds the values of IQVIA. (experience)

Responsibilities

  • Develop study-specific action plans with research sites to accelerate recruitment and support procedural training.
  • Educate healthcare professionals and their staff on study protocols related to clinical trials.
  • Partner with referral networks to identify potential trial participants.
  • Maintain and analyze customer records to tailor strategies for pre-screening, screening, and enrollment.
  • Complete internal reporting and organize group events to optimize program delivery.
  • Address and manage objections effectively.
  • Stay current with technical knowledge in relevant therapeutic areas.
  • Develop study-specific action plans with research sites to accelerate recruitment and support procedural training.
  • Educate healthcare professionals and their staff on study protocols related to clinical trials.
  • Partner with referral networks to identify potential trial participants.
  • Maintain and analyze customer records to tailor strategies for pre-screening, screening, and enrollment.
  • Complete internal reporting and organize group events to optimize program delivery.
  • Address and manage objections effectively.
  • Stay current with technical knowledge in relevant therapeutic areas.

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