Parexel

Patient Recruitment Specialist - FSP

Parexel  •  North Carolina (Remote)  •  3 days ago
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Job Description

When our values align, there's no limit to what we can achieve.

At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

The Patient Recruitment Specialist manages the execution of the recruitment strategy and is accountable for all patient recruitment deliverables for their assigned studies. The Patient Recruitment Specialist has strong knowledge of patient recruitment processes and will be responsible for the delivery of moderate to highly complex recruitment strategies (high number and complexity of recruitment tactics) across multiple clinical trials.

Role Responsibilities:

  • Accountable for the delivery of the recruitment strategy and tactics against the approved plan, timeline, and budget.
  • Coordinate with other patient recruitment team members, the clinical study team, and other functional lines to ensure all patient recruitment deliverables are met.
  • Provide oversight for vendors contracted to deliver patient recruitment and retention services.
  • Monitor if recruitment strategies are meeting clinical trial enrollment and timeline goals, including country and site segmentation needs and enrollment of diverse and underrepresented populations.
  • Proactively identify recruitment and retention risks, provide recommended mitigations, and oversee execution of contingency plans.
  • Partner with other recruitment team members, the clinical study team, other internal stakeholders, and vendors to appropriately manage escalations and resolve issues.
  • Support the delivery of innovative solutions for patient recruitment and retention.
  • Lead study close-out activities including analysis of lessons learned and best practices.

QUALIFICATIONS

  • Bachelor's degree in business, science, marketing, or related discipline.
  • Candidate should have 3+ years of pharmaceutical research experience, with at least 1-3 years of experience specifically in patient recruitment at a vendor, CRO, or sponsor company. Ideally, a mix of the three.
  • Strong knowledge of patient recruitment and retention strategies including, but not limited to: direct to patient outreach, digital/mobile and traditional media, site management organizations, advocacy groups, patient networks, and on-site support. At least 1-3 years of experience leading the execution of outreach campaigns, global recruitment strategies, or other complex recruitment and retention solutions is preferred.
  • Experience with the development of materials for patient recruitment, health education, or marketing.
  • Familiarity with using style guidelines and health literacy principles.
  • Strong knowledge of capturing, analyzing, and reporting on recruitment metrics and other key performance indicators.
  • Strong knowledge of clinical research processes including study start-up, site management, and vendor management.
  • Experience in collaborating with legal and privacy officers to ensure processes and systems are compliant.
  • 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.
  • Exceptional interpersonal skills, including ability to present, influence, persuade, negotiate, and moderate conflict.
  • Ability to be flexible, adapt to change, and work under tight deadlines on several projects with specific and unique requirements, while providing attention to detail and high-quality work.
  • Ability to work outside of core business hours as needed to support global clinical trials, initiatives, or meet required deliverables.

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EEO Disclaimer
Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

Parexel

About Parexel

Parexel is among the world’s largest clinical research organizations (CROs), providing the full range of Phase I to IV clinical development services to help life-saving treatments reach patients faster. Leveraging the breadth of our clinical, regulatory and therapeutic expertise, our team of more than 21,000 global professionals collaborates with biopharmaceutical leaders, emerging innovators and sites to design and deliver clinical trials with patients in mind, increasing access and participation to make clinical research a care option for anyone, anywhere. Our depth of industry knowledge and strong track record gained over the past 40 years is moving the industry forward and advancing clinical research in healthcare’s most complex areas, while our innovation ecosystem offers the best solutions to make every phase of the clinical trial process more efficient. With the people, insight and focus on operational excellence, we work every day to treat patients with dignity and continuously learn from their experiences, so every trial makes a difference. For more information, visit parexel.com.

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Industry
Chemicals & Materials
Company Size
10,000+ employees
Headquarters
Raleigh, North Carolina
Year Founded
Unknown
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