What are the responsibilities and job description for the Clinical Trial Prpject Manager (Boston, MA) position at CEDENT?
Hybrid role
About the Role
As a Clinical Trial Project Manager, you will lead end-to-end project execution, ensuring seamless collaboration across academic medical centers, community clinic sites, and sponsors. You’ll oversee a variety of study types, including but not limited to Phase 1, Phase 2, and Phase 4 trials, as well as observational and interventional studies, delivering innovative solutions to meet the evolving needs of our clients and patients.
This role will integrate with our Perspective Evidence Generation Team, a specialized group seated within the R&D, Medical & Evidence functions at ZS.
This role offers flexibility to start as a part-time or outsourced position, with the potential to transition into a full-time role based on performance.
What We’re Looking For
? Experience: At least 10 years in clinical trial project management, with a focus on working with academic medical sites, community clinics, and managing sponsor relationships.
? Knowledge: Strong understanding of ICH guidelines, industry best practices, regulatory processes, and real-world evidence studies.
? Expertise: Proven experience managing diverse study types, including early-phase trials, late-phase trials, and both observational and interventional studies.
? Communication: Proven ability to liaise effectively with sponsors, sites, and other stakeholders, ensuring clear, professional, and proactive communication at every stage of the project.
? Training: Formal training in project management; certifications such as PMP, PRINCE2, or equivalent are a plus.
Additionally, certifications specific to clinical trials, such as:
- Certified Clinical Research Professional (CCRP),
- Certified Clinical Research Coordinator (CCRC),
- Certified Clinical Research Associate (CCRA),
- Certified Clinical Project Manager (CCPM) by recognized institutions.
? Leadership: Demonstrated ability to lead cross-functional teams and ensure projects are delivered on time, within budget, and to the highest quality standards.
About the Role
As a Clinical Trial Project Manager, you will lead end-to-end project execution, ensuring seamless collaboration across academic medical centers, community clinic sites, and sponsors. You’ll oversee a variety of study types, including but not limited to Phase 1, Phase 2, and Phase 4 trials, as well as observational and interventional studies, delivering innovative solutions to meet the evolving needs of our clients and patients.
This role will integrate with our Perspective Evidence Generation Team, a specialized group seated within the R&D, Medical & Evidence functions at ZS.
This role offers flexibility to start as a part-time or outsourced position, with the potential to transition into a full-time role based on performance.
What We’re Looking For
? Experience: At least 10 years in clinical trial project management, with a focus on working with academic medical sites, community clinics, and managing sponsor relationships.
? Knowledge: Strong understanding of ICH guidelines, industry best practices, regulatory processes, and real-world evidence studies.
? Expertise: Proven experience managing diverse study types, including early-phase trials, late-phase trials, and both observational and interventional studies.
? Communication: Proven ability to liaise effectively with sponsors, sites, and other stakeholders, ensuring clear, professional, and proactive communication at every stage of the project.
? Training: Formal training in project management; certifications such as PMP, PRINCE2, or equivalent are a plus.
Additionally, certifications specific to clinical trials, such as:
- Certified Clinical Research Professional (CCRP),
- Certified Clinical Research Coordinator (CCRC),
- Certified Clinical Research Associate (CCRA),
- Certified Clinical Project Manager (CCPM) by recognized institutions.
? Leadership: Demonstrated ability to lead cross-functional teams and ensure projects are delivered on time, within budget, and to the highest quality standards.
