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Pfizer

Patient Recruitment Specialist I – Secondment, 12 Months

Pfizer

. Manage core activities after internal approval of study level Participant Recruitment & Retention (PRR) materials to ensure the successful delivery of PRR tactics across all countries .

Posted 5/7/2026full-timeLake Forest • Illinois • 🇺🇸 United StatesMid-LevelSeniorWebsite

About the role

Key responsibilities & impact
  • Manage core activities after internal approval of study level Participant Recruitment & Retention (PRR) materials to ensure the successful delivery of PRR tactics across all countries
  • Partner with the CDH vendor to lead activities across multiple clinical trials
  • Accountable for the delivery of the recruitment strategy and tactics against the approved plan, timeline, and budget
  • Provide oversight for CDH vendor contracted to execute CDH tasks, which include: Customization of study level PRR materials for each country on a clinical trial, ensuring content is compliant with country regulations and meets needs of local population
  • Translation of study level PRR materials for all required languages
  • Providing package of country level materials for IRB/EC submission
  • Fulfillment of R&R site kit materials through print/ship or digital delivery to all sites
  • Coordinate with other patient recruitment team members, the clinical study team, and other functional lines to gather study details needed to execute CDH tasks
  • Partner with submission managers and other country colleagues to ensure PRR materials are submitted to all IRB/ECs and monitor approvals
  • Partner with CDH vendor to revise materials if required due to IRB/EC query or protocol amendment
  • Partner with other recruitment team members, the clinical study team, other internal stakeholders, and CDH vendor to appropriately manage escalations and resolve issues

Requirements

What you’ll need
  • Applicant must have a bachelor's degree with 0+ years of experience
  • Clinical research or clinical trial experience
  • Knowledge of clinical research processes including study start-up, site management, and vendor management
  • Proficient in Microsoft office applications (Outlook, Word, PowerPoint, Excel, TEAMS)
  • Effective verbal and written communication skills in relating to colleagues and associates both inside and outside the organization; ability to work independently and in a matrixed environment
  • Well-developed planning, observation, analytical and problem-solving, and time management skills
  • Associate's degree with 4+ years of experience; OR a high school diploma (or equivalent) and 6+ years of relevant experience

Benefits

Comp & perks
  • Global Any Pfizer Site
  • Eligible for Relocation Package – NO
  • Position is considered Flexible
  • Professional growth opportunity

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools
clinical researchclinical trialstudy start-upsite managementvendor managementrecruitment strategytactics deliverymaterial customizationtranslationIRB/EC submission
Soft Skills
effective communicationindependent workmatrixed environmentplanningobservationanalytical skillsproblem-solvingtime management
Certifications
bachelor's degreeassociate's degreehigh school diploma