• Parexel (Boston, MA)
    **Job Summary:** Core member of the Clinical Trial Team (CTT), independently managing all vendor-related aspects of global clinical trial (s) to deliver ... + Very strong vendor management skills; outsourcing, contracting, and sourcing of clinical trial services + Results-driven: demonstrated ability of completing… more
    DirectEmployers Association (11/23/25)
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  • Parexel (Boston, MA)
    …at the trial level throughout the preparation, conduct and reporting phase of clinical trial . During the clinical trial , SP is responsible ... execute medical oversight from the Trial Design Outline (TDO) kick off to the Clinical Trial Report (CTR). SP is a core member of the Trial Team and the… more
    DirectEmployers Association (10/13/25)
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  • Parexel (Boston, MA)
    …activities associated with the set-up, running and close-out of sites in a clinical trial . **Monitoring Responsibilities and Study Conduct:** + Ensure proper ... timelines and quality + Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites from site activation… more
    DirectEmployers Association (11/14/25)
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  • Parexel (Boston, MA)
    …and logistics. - Lead cross-functional study teams, manage vendor relationships, and oversee clinical trial biosamples and data monitoring. - Oversee and manage ... **PXL is seeking a clinical operations lead with expertise in clinical...clinical trial biosamples and data monitoring and...clinical trial biosamples and data monitoring and completeness from collection… more
    DirectEmployers Association (10/10/25)
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  • Parexel (Boston, MA)
    …Review Officer who is looking to draw upon their wealth of experience in clinical trial design and drug development to join Parexel's highly recognized ... experience with expert level industry or regulatory knowledge experience in Clinical Development/ Clinical Trial Design, Clinical Strategy, and expertise… more
    DirectEmployers Association (10/10/25)
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  • Parexel (Boston, MA)
    …at the trial level throughout the preparation, conduct and reporting phase of clinical trial . During the clinical trial , SP is responsible ... execute medical oversight from the Trial Design Outline (TDO) kick off to the Clinical Trial Report (CTR). SP is a core member of the Trial Team and the… more
    DirectEmployers Association (11/23/25)
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  • Parexel (Boston, MA)
    …client in making budget and contractual decisions against the impacts to client clinical trial timelines + Follow client processes to develop, negotiate, track ... to develop and oversee the global site budget process + Work with clinical trial sites and directly negotiate cost, business and contractual terms and conditions… more
    DirectEmployers Association (10/17/25)
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  • Parexel (Boston, MA)
    clinical trials. Performs other duties as necessary to ensure optimal clinical trial execution. **Key Accountabilities** **:** **Study Team Support** + ... manual, sample collection procedures and presentation slides) + Manages acquisition of clinical trial samples + Provides support for sample related matters to … more
    DirectEmployers Association (11/07/25)
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  • Parexel (Boston, MA)
    …entities within the CTMS system to then enable site association with a clinical trial ; routinely reconciles unique identifiers to ensure adherence to Sponsor ... sites and may register key essential documents into the Trial Master File; Captures relevant study, country and site...protocol specific requirements that may be defined by the clinical study team - Supports the identification of Investigator… more
    DirectEmployers Association (11/21/25)
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  • Parexel (Boston, MA)
    …7+ years experience in pharmaceutical/biotech clinical data management / Biometrics ( clinical trial data and/or Real World Data) + Medical affairs experience ... leading DM study teams, overseeing trial data activities, and collecting clinical trial and/or Real World Data, with a good understanding of molecule and… more
    DirectEmployers Association (10/10/25)
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