• Merck & Co. (North Wales, PA)
    Job DescriptionOphthalmology- Study Manager :Job SummaryThis position leads the operational planning and execution of one or more clinical trials or ... (eg, study team, country teams, vendors, committees) in support of clinical study objectives.-Accountable for managing any study specific partners… more
    HireLifeScience (09/05/25)
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  • Merck & Co. (Upper Gwynedd, PA)
    …Arrangements:RemoteShift:1st - DayValid Driving License:NoHazardous Material(s):NoRequired Skills:Adaptability, Clinical Quality Management, Clinical Study ... for, management and follow up of regulatory inspections.Operational Quality Management:The Clinical Quality Operations Manager is accountable for overseeing the… more
    HireLifeScience (09/09/25)
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  • Merck & Co. (North Wales, PA)
    …macular degeneration), thyroid eye disease. Experience in developing protocols and study related documents for ophthalmology clinical trials. Experience ... related study materials (eg, ICF documents / amendments); Partners with the Study Manager on study deliverables.Ensuring CRF design supports data… more
    HireLifeScience (09/05/25)
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  • Senior Scientist Study Manager

    Merck (West Point, PA)
    **Job Description** Ophthalmology Study Manager : **Job Summary** This position leads the operational planning and execution of one or more clinical trials or ... stakeholders (eg, study team, country teams, vendors, committees) in support of clinical study objectives. + Accountable for managing any study specific… more
    Merck (09/05/25)
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  • Senior Manager , Clinical Project…

    Sumitomo Pharma (Harrisburg, PA)
    …and monitoring reports relating to the studies . + Prepare and deliver program/ study updates. + Coordinates the delivery of clinical trial supplies in ... study team to design, develop and deliver the clinical study to agree upon timelines. +...and vendors. + Oversees and monitors the management of clinical studies ensuring they are conducted in… more
    Sumitomo Pharma (09/03/25)
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  • Oncology Early Stage Clinical Scientist…

    Pfizer (Collegeville, PA)
    …of the clinical protocol and may participate as an individual contributor on clinical study teams and clinical subteams to meet enrollment and ... will also be mentored/obtain guidance from a more senior study clinician. Depending on experience , you may...Early Stage Development (OESD) is represented as needed within clinical study teams. **KEY POSITION RESPONSIBILITIES** +… more
    Pfizer (08/15/25)
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  • Senior Clinical Trial Manager

    ICON Clinical Research (Blue Bell, PA)
    Senior Clinical Trial Manager - United States- Remote...study . + At least 10+ years of relevant experience in clinical trial management. + Preferred: ... clinical development. We are currently seeking a **Senior Clinical Trial Manager ** to join our diverse...crucial role in ensuring the successful delivery of all clinical aspects of the studies . Your expertise… more
    ICON Clinical Research (08/30/25)
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  • Clinical Trial Manager

    System One (Pittsburgh, PA)
    Title: Clinical Trial Manager Location: Onsite, Oakland, PA Schedule: M-F 8 am-5 pm Type: Direct/Permanent Overview: A distinguished research university is ... currently in search of a Clinical Trial Manager to play a key...to play a key role in facilitating and overseeing clinical trials and multi-site studies . This position… more
    System One (07/15/25)
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  • Clinical Research Coordinator A/B…

    University of Pennsylvania (Philadelphia, PA)
    Clinical Research Coordinator A : BS degree required. 1-2 years related experience in research and clinical study methodologies or equivalent combination ... research related presentations. Works closely with the Principal Investigator, manager , and study team to identify problems...Coordinator B : BS degree required. 2-3 years related experience in research and clinical study more
    University of Pennsylvania (08/03/25)
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  • Clinical Research Coordinator B/C

    University of Pennsylvania (Philadelphia, PA)
    …quality of the clinical trial data and records, scheduling and conducting study initiation and monitoring visits, and participating in ongoing study protocol ... study data. Obtain records required to complete case report forms. Update/maintain study record in the Clinical Trials Management System (CTMS) in real-time.… more
    University of Pennsylvania (08/08/25)
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