CDH Patient Recruitment Specialist I (Secondment 12 Months)

WHY PATIENTS NEED YOU

The Content Delivery Hub Patient Recruitment Specialist manages core activities after internal approval of study level Participant Recruitment & Retention (PRR) materials to ensure the successful delivery of PRR tactics across all countries. The CDH Patient Recruitment Specialist will partner with the CDH vendor to lead these activities across multiple clinical trials.

WHAT YOU WILL ACHIEVE

• 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.

HOW YOU WILL ACHIEVE IT

• Coordinate with other patient recruitment team members the clinical study team and other functional lines to gather study details needed to execute CDH tasks including but not limited to: required languages required materials for each country submissions timelines site lists and print quantities.

• 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.

• Ensure the CDH vendor is delivering against the approved plan timeline and budget.

QUALIFICATIONS

Must-Have

• Applicant must have a bachelors 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.

Nice-to-Have

• Associates degree with 4 years of experience; OR a high school diploma(or equivalent) and 6 years of relevant experience

OTHER JOB DETAILS

• Last Date to Apply for Job:April 20 2026

• Additional Location Information: Global Any Pfizer Site

• Eligible for Relocation Package NO

• Secondment12 months

• If you are currently in a driving position with a fleet vehicle and this secondment does not require driving as an essential function of the position for12 months or longer you will be required to turn in your fleet vehicle for the duration of the non-driving secondment. Please refer to the Fleet Policy and Procedures document for more information.

• There will be no change to your current work location.

• Position is considered Flexible and colleagues are expected to comply with Log In For Your Day(LIFYD) requirements at site location (e.g. about 2.5 days a week in office).

• Note: This secondment offers a valuable opportunity for professional growth. It will need to be funded by the secondees home market.

Relocation assistance may be available based on business needs and/or eligibility.

Candidates must be authorized to be employed in the U.S. by any employer.

U.S. work visa sponsorship (such as TN O-1 H-1B etc.) is not available for this role now or in the future.