Current jobs related to Clinical Study Specialist - Uxbridge Greater London - Proclinical Staffing

  • Clinical Study Specialist

    5 months ago

    Uxbridge, United Kingdom Regeneron Pharmaceuticals Inc. Full time

    The Clinical Study Specialist (CSS) provides technical and administrative support to the clinical study team(s) responsible for clinical trial execution. The CSS may be assigned to support the execution of one or more studies across a program. The CSS receives assignments from the Clinical Study Lead or Clinical Study Associate Manager. The CSS will support...

  • Clinical Study Coordinator

    3 weeks ago

    Uxbridge, United Kingdom Pharmiweb Full time

    Job Title: Clinical Study SpecialistRegeneron is seeking a highly skilled Clinical Study Specialist to join our team. As a Clinical Study Specialist, you will provide technical and administrative support to our clinical study teams, ensuring the successful execution of clinical trials.Key Responsibilities:Organize and deliver high-quality reports and metrics...

  • Clinical Study Coordinator

    3 weeks ago

    Uxbridge, United Kingdom Pharmiweb Full time

    Job Title: Clinical Study SpecialistRegeneron is seeking a highly skilled Clinical Study Specialist to join our team. As a Clinical Study Specialist, you will provide technical and administrative support to our clinical study teams, ensuring the successful execution of clinical trials.Key Responsibilities:Organize and deliver high-quality reports and metrics...

  • Clinical Study Coordinator

    3 weeks ago

    Uxbridge, United Kingdom Pharmiweb Full time

    Job SummaryWe are seeking a highly organized and detail-oriented Clinical Study Specialist to join our team. As a Clinical Study Specialist, you will provide technical and administrative support to our clinical study team, ensuring the successful execution of clinical trials.Key ResponsibilitiesOrganize and deliver high-quality reports and metrics to the...

  • Clinical Study Coordinator

    3 weeks ago

    Uxbridge, United Kingdom Pharmiweb Full time

    Job SummaryWe are seeking a highly organized and detail-oriented Clinical Study Specialist to join our team. As a Clinical Study Specialist, you will provide technical and administrative support to our clinical study team, ensuring the successful execution of clinical trials.Key ResponsibilitiesOrganize and deliver high-quality reports and metrics to the...

  • Temp-Clinical Study Specialist

    3 weeks ago

    Uxbridge, United Kingdom Regeneron Full time

    The Clinical Study Specialist (CSS) provides technical and administrative support to the clinical study team(s) responsible for clinical trial execution. The CSS may be assigned to support the execution of one or more studies across a program. The CSS receives assignments from the Clinical Study Lead or Clinical Study Associate Manager. The CSS will support...

  • Clinical Study Specialist

    5 months ago

    Uxbridge, United Kingdom Regeneron Pharmaceuticals Inc. Full time

    The Clinical Study Specialist (CSS) provides technical and administrative support to the clinical study team(s) responsible for clinical trial execution. The CSS may be assigned to support the execution of one or more studies across a program. The CSS receives assignments from the Clinical Study Lead or Clinical Study Associate Manager. The CSS will support...

  • Temp-Clinical Study Specialist

    3 weeks ago

    Uxbridge, United Kingdom Pharmiweb Full time

    The Clinical Study Specialist (CSS) provides technical and administrative support to the clinical study team(s) responsible for clinical trial execution. The CSS may be assigned to support the execution of one or more studies across a program. The CSS receives assignments from the Clinical Study Lead or Clinical Study Associate Manager. The CSS will support...

  • Clinical Study Manager

    1 month ago

    Uxbridge, United Kingdom Amgen Inc. (IR) Full time

    Job SummaryWe are seeking a highly skilled Clinical Study Manager to join our team at Amgen Inc. (IR). As a key member of our Clinical Payments Systems team, you will be responsible for managing and coordinating clinical budget and related pricing strategy services for Clinical Study Teams.Key ResponsibilitiesManage and coordinate clinical budget and related...

  • Clinical Study Manager

    1 month ago

    Uxbridge, United Kingdom Amgen Inc. (IR) Full time

    Job SummaryWe are seeking a highly skilled Clinical Study Manager to join our team at Amgen Inc. (IR). As a key member of our Clinical Payments Systems team, you will be responsible for managing and coordinating clinical budget and related pricing strategy services for Clinical Study Teams.Key ResponsibilitiesManage and coordinate clinical budget and related...

  • Senior Clinical Study Manager

    6 hours ago

    Uxbridge, United Kingdom Regeneron Pharmaceuticals, Inc Full time

    Job Summary: We are seeking a highly skilled and experienced Senior Clinical Study Manager to lead the global execution of assigned large and/or complex clinical trials from study design, through execution, to study close out.Key Responsibilities:Leads the cross-functional study team responsible for clinical study delivery and is the primary point of contact...

  • Clinical Study Manager

    4 weeks ago

    Uxbridge, United Kingdom Regeneron Full time

    Job Title: Clinical Study ManagerRegeneron is seeking a highly skilled Clinical Study Manager to join our team. As a key member of our Clinical Operations department, you will be responsible for planning and delivering European Union Clinical Trials Regulation (EUCTR) reporting according to the Part II requirements outlined by the European Medicines Agency...

  • Clinical Study Manager

    4 weeks ago

    Uxbridge, United Kingdom Regeneron Full time

    Job Title: Clinical Study ManagerRegeneron is seeking a highly skilled Clinical Study Manager to join our team. As a key member of our Clinical Operations department, you will be responsible for planning and delivering European Union Clinical Trials Regulation (EUCTR) reporting according to the Part II requirements outlined by the European Medicines Agency...

  • Clinical Data Specialist

    4 weeks ago

    London, Greater London, United Kingdom Worldwide Clinical Trials Full time

    Job Summary: We are seeking a skilled Clinical Data Specialist to join our team at Worldwide Clinical Trials. The successful candidate will be responsible for utilizing standard and/or sponsor custom dictionaries to code Adverse Events, Medical and Surgical Histories, Medications, and other sponsor-requested medical terminology required for projects. Key...

  • Clinical Data Specialist

    4 weeks ago

    London, Greater London, United Kingdom Worldwide Clinical Trials Full time

    Job Summary: We are seeking a skilled Clinical Data Specialist to join our team at Worldwide Clinical Trials. The successful candidate will be responsible for utilizing standard and/or sponsor custom dictionaries to code Adverse Events, Medical and Surgical Histories, Medications, and other sponsor-requested medical terminology required for projects. Key...

  • Clinical Study Manager

    1 month ago

    Uxbridge, United Kingdom Amgen Inc. (IR) Full time

    Job Title: Clinical Study ManagerLocation: Flexible Commuter / Hybrid, United Kingdom - Cambridge, United Kingdom - UxbridgeTime Type: Full timeAbout the RoleIn this critical position, you will oversee and coordinate clinical budget and related pricing strategy services for Clinical Study Teams to execute Clinical Trials or Ancillary Services Agreements. You...

  • Clinical Study Manager

    1 month ago

    Uxbridge, United Kingdom Amgen Inc. (IR) Full time

    Job Title: Clinical Study ManagerLocation: Flexible Commuter / Hybrid, United Kingdom - Cambridge, United Kingdom - UxbridgeTime Type: Full timeAbout the RoleIn this critical position, you will oversee and coordinate clinical budget and related pricing strategy services for Clinical Study Teams to execute Clinical Trials or Ancillary Services Agreements. You...

  • Clinical Study Manager

    1 month ago

    Uxbridge, United Kingdom Amgen Inc. (IR) Full time

    Job Title: Clinical Study ManagerLocation: Flexible Commuter / Hybrid, United Kingdom - Cambridge, United Kingdom - UxbridgeTime Type: Full timeAbout the RoleIn this critical position, you will oversee the management and coordination of clinical budget and related pricing strategy services for Clinical Study Teams. Your primary objective will be to execute...

  • Clinical Study Manager

    1 month ago

    Uxbridge, United Kingdom Amgen Inc. (IR) Full time

    Job Title: Clinical Study ManagerLocation: Flexible Commuter / Hybrid, United Kingdom - Cambridge, United Kingdom - UxbridgeTime Type: Full timeAbout the RoleIn this critical position, you will oversee the management and coordination of clinical budget and related pricing strategy services for Clinical Study Teams. Your primary objective will be to execute...

  • Clinical Study Manager

    3 weeks ago

    Uxbridge, United Kingdom Amgen Inc. (IR) Full time

    Job Title: Clinical Study ManagerLocation: Flexible Commuter / Hybrid, United Kingdom - Cambridge, United Kingdom - UxbridgeTime Type: Full timeAbout the RoleIn this critical position, you will oversee and coordinate clinical budget and related pricing strategy services for Clinical Study Teams to execute Clinical Trials or Ancillary Services Agreements. You...

Clinical Study Specialist

2 months ago

Uxbridge Greater London, United Kingdom Proclinical Staffing Full time

Proclinical is seeking four Contract Clinical Study Specialists for a large pharmaceutical company based in London. This role offers flexible working and the potential for a permanent position after a 12-month rolling contract. The Contract Clinical Study Specialist provides technical and administrative support to the clinical study team(s) responsible for clinical trial execution. The role may involve supporting one or more studies across a program and may include both internally sourced studies and studies outsourced to Clinical Research Organizations (CROs).
Organize and deliver analysable reports and metrics to the clinical study lead.
Schedule and coordinate meetings, prepare agendas, presentation materials, and minutes for clinical study team meetings and other study-related meetings.
Collate data for assessments such as feasibility and site selection and review site usability database.
Contribute to the review of study documents such as informed consent forms, case report forms, and facilitate study document reviews per company standard operating procedures.
Compile study manuals including but not limited to: study reference binders and manuals and maintain versioning of study reference materials.
Track site activation, enrolment, and monitoring visits to projected plans, and escalate any issues or delays with site activation or deviations from the monitoring plan.
Monitor and update investigator/site status for the trial, and support with clinical trial registry postings.
Perform scheduled reconciliations of study Trial Master File (TMF) with clinical study lead guidance.
Manage and maintain team SharePoint and/or shared drive sites, as needed.
Contribute to line listings review for Blind Data Review Meeting (BDRM).
Ability to manage multiple tasks and projects simultaneously.
Knowledge of clinical trial processes and procedures.
Familiarity with SharePoint and/or shared drive sites.

Alternatively, for further details or to talk directly to a life sciences recruitment specialist, please request a call back at the top of this page.
Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe.