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.
PXL FSP – Join an organization shaping smarter, faster clinical development
PXL FSP is seeking a detail‑oriented and proactive Feasibility Study Manager to support the delivery of high‑quality global feasibility assessments. This role is ideal for someone who thrives in a fast‑paced, data‑driven environment and enjoys collaborating cross‑functionally to ensure clinical programs launch with the strongest foundation possible.
Key ResponsibilitiesSurvey Design & Configuration- Transform draft feasibility questionnaires into an electronic survey platform with clear, intuitive formatting.
- Apply branching logic, conditional pathways, and scoring algorithms in alignment with the Feasibility Lead’s specifications.
- Build survey reporting templates directly within the platform or through external systems as needed.
- Perform quality checks on potential investigators before survey deployment.
- Support verification of available CDAs prior to launch.
- Upload targeted site and investigator lists into the survey management system, ensuring accuracy and completeness.
- Lead survey launch activities and oversee ongoing monitoring, including:
- Delegating surveys appropriately
- Tracking and reconciling survey status
- Ensuring thorough documentation of site notes and survey details
- Identifying and consolidating invalid contact information
- Conduct proactive research to update missing or incorrect contact details, ensuring seamless engagement and response tracking.
- Monitor country‑level response metrics to support early risk identification and mitigation planning.
- Execute the agreed site‑identification strategy, including application of priority site designations.
- Implement the communication plan using approved study summaries, templates, and designated system email origins.
- Facilitate timely revisions to survey content, scoring, and site/country lists as needed throughout survey duration.
- Track CDA negotiation status for participating sites and communicate internal updates.
- Oversee survey closure, including final site notifications and completion of assigned wrap‑up tasks.
- Education: Bachelor’s degree or equivalent.
- Experience: 3–5 years of relevant industry experience (clinical research, feasibility, site engagement, project coordination, or related areas).
#LI-KW1
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.
Top Skills
What We Do
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 With HeartTM 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.
Community Guidelines
Because Parexel’s social media channels are open to the general public and employees, we are not responsible for views expressed other than our own. However, we do not tolerate posts that are:
• Abusive, harassing or threatening to others.
• Defamatory, offensive, obscene, vulgar or depicting violence.
• Hateful targeting by race/ethnicity, age, color, creed, religion, gender,
sexual preference or orientation, nationality or political beliefs.
• Sexually explicit or pornographic.
• Fraudulent, deceptive, libelous, misleading or unlawful.
• Referencing criminal or illegal activity.
• Spamming.
We reserve the right to remove any comments that do not adhere to our guidelines as well as report users who violate the rules of our page.
.png)
