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Clinical Protocol Data Manager Jobs in Welwyn Garden City, England

93 Jobs

  • 3.7
    GlaxoSmithKline – Stevenage, England
    24 days ago 24d
    programmer for GSK clinical trials, accountable for creating, verifying, and documenting analyses of clinicaldata while adhering… adhering to study protocols, analysis plans and GSK / industry standards. Responsibilities: Plan and manage programming activities…
  • 2.8
    Eisai – Hatfield, East of England, England
    5 days ago 5d
    execution of the study from protocol concept to final report including interpretation of clinicaldata Serves as the Medical Monitor… integration of the Clinical Development Plan (CDP) and the Drug Development Plan Leads the development of ClinicalProtocols to meet CDP…
  • 2.8
    Eisai – Hatfield, East of England, England
    NEW
    into the Clinical Development Plan (CDP) and Drug Development Plan (DDP) Leading the development of ClinicalProtocols to meet… Serving as Study Director/Clinical Pharmacology Lead and driving the execution of the study from protocol concept to final report…
  • 2.8
    CRF Health – Hammersmith, England
    HOT
    Project Managers to ensure complete review of application design for end user use and adherence to a clinicalprotocol Perform… requirements gathered and interpretation of the client clinicalprotocol Present eCOA solutions at client design review and testing…
  • 2.8
    CRF Health – Hammersmith, England
    HOT
    Project Managers to ensure complete review of application design for end user use and adherence to a clinicalprotocol; supporting… requirements gathered and interpretation of the client clinicalprotocol Create standard online reports in TrialManager web portal…
  • 2.8
    Eisai – Hatfield, East of England, England
    24 days ago 24d
    execution of the study from protocol concept to final report, including interpretation of clinicaldata Serving as the Medical… and drug development plans - Leading the development of clinicalprotocols to meet CDP objectives Serving as a Study Director and…
  • 2.8
    Eisai – Hatfield, East of England, England
    18 days ago 18d
    Develops Protocol Concept Sheets (PCS1 and PCS2) for review by CRAB Develops/reviews ClinicalProtocolsManages medical writer… reporting of clinical programs/ trials Clinical Research Protocols Reviews and Revises ClinicalProtocols as follows:…
  • 3.3
    PAREXEL – Uxbridge, England
    12 days ago 12d
    clinical systems (e.g. CTMS, EDC, IVRS, and SIS) and ensure timely and high quality data entry compliance from sites, manage and… integrity of study implementation and adherence to study protocol at clinical sites, and perform problem-solving to address and resolve…
  • 3.9
    Boston Scientific – Hemel Hempstead, England
    NEW
    input into clinicalprotocol development especially as it relates to the feasibility of collecting critical endpoint data for the… efficient day-to-day execution of Boston Scientific clinical trials according to protocol requirements, world-wide regulatory body compliance…
  • 3.3
    PAREXEL – Uxbridge, England
    NEW
    integrity of study implementation and adherence to study protocol at clinical sites, and perform problem-solving to address and resolve… are not required to be on site. The Clinical Site Manager (CSM) is the clinical sites direct point of contact and accountable…
  • 3.4
    Clinical Professionals Limited – United Kingdom
    11 days ago 11d
    understanding of clinical research methodology - from study concept, protocol and CRF design, CSR development and clinicaldata review… CPL, CD, Clinical director, clinical project director, associate director, ad, trial lead, trial manager, study manager, study lead…
  • 4.1
    Zoek – Charing Cross, England
    NEW
    Operating Procedures and the specific protocols as designated by the trial Sponsors and Clinical Research Organisations. The Role… The Primary purpose of the Clinical Trials Administrator is to assist the Clinical Trials Manager (CTM), maintain and co-ordinate…
  • 3.4
    Clinical Professionals Limited – United Kingdom
    18 days ago 18d
    the Director, Clinical Research. Key Responsibilities: Lead phase II & III Oncology programmes Protocol development… led and managed global programmes & teams Associate Clinical Director, Associate Clinical Research Director, Clinical Portfolio…
  • 3.3
    PAREXEL – Uxbridge, England
    12 days ago 12d
    building has plenty of free parking . The Initiation Clinical Site Manager(iCSM) specialises in Pre SIV activities will be assigned… experience or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology In…
  • 3.4
    Clinical Professionals Limited – London, England
    30+ days ago 30d+
    training (site initiation), support, clinical monitoring and management of GCP non-compliance Protocol amendments as required Regular… freelance Clinical Programme Manager to manage studies in UK and Europe. Location: Home based Position: Clinical Programme…
  • 3.7
    Barrington James Ltd – London, England
    21 days ago 21d
    the project team Assist the project managers in the preparation and review of protocols Negotiates investment budgets and assists… need. They are looking to expand their team within Senior Clinical Research Associates. The company offers both a professional…
  • 3.4
    IQVIA Holdings, Inc. – London, England
    10 days ago 10d
    and skill in applying, applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International… and 7 years’ clinical research experience including 4 years’ project management experience and experience in clinical operations;…
  • 2.8
    Execupharm Uk Limited – London, England
    6 days ago 6d
    operational aspects of one or more clinical studies from protocol feasibility through database release. Their primary deliverable is… Global Clinical Project Manager A Leading Top Biotech are looking for the best talent to join their expanding team. If you…
  • 2.8
    Eisai – Hatfield, East of England, England
    26 days ago 26d
    management, and datamanager teams on strategic designs of studies; development, review and approval of clinical study protocols; review… that he/she will be responsible for designing clinical trial, performing data analysis, overseeing CRO activities, validating TLGs…
  • 2.8
    Eisai – Hatfield, East of England, England
    18 days ago 18d
    Epilepsy Portfolio through the utilization of clinical, economic, and quality data across multiple stakeholders in the C and D Suite… develop and manage relationships, and tailor communications to a variety of audiences in both a B2B and clinical context, especially…
  • 2.8
    Eisai – Hatfield, East of England, England
    11 days ago 11d
    initiatives, and APMs Understand relevant quality metrics, clinicalprotocols, care pathways, cost of care/episode of care payment models… Oncology Portfolio through the utilization of clinical, economic, and quality data resources across multiple stakeholders (included…
  • 2.8
    Eisai – Hatfield, East of England, England
    8 days ago 8d
    prepares and at times may direct, the writing of PCSs, protocols and protocol amendments - Independently prepares and at times… incumbent ensures timely completion, accuracy and quality of all clinical and submission documentation across all aspects of the compounds…
  • 2.8
    Eisai – Hatfield, East of England, England
    18 days ago 18d
    deliverables and on QA of data outputs Function as lead statistician in global registration trials and manage all related statistical… for multiple clinical trials, including SAPs, TLG shells and specifications of variable derivation. Support clinical trial related…
  • 3.4
    Inventiv Health Clinical UK Ltd – London, England
    13 days ago 13d
    sites Review draft protocols for completeness and feasibility Develop Case Report Forms for clinical trials Present (e.g… CRFs and other clinicaldata, in-house, for completeness and accuracy; generate queries Resolve queries of CRF data with study site…
  • 5.0
    Pop Science – City of London, England
    4 days ago 4d
    World data through to site and study close-out. As a CRA Manager youwill oversee an in-house and remote team of Clinical Research… provide coaching to CRAs as needed to ensure compliance with protocol and GCP requirements Comply with all applicable laws…
  • 3.4
    Bioclinica – London, England
    19 days ago 19d
    Assists Clinical Project Managers in maintaining, reviewing and communicating project progress by: Monitoring internal data flow… (SOPs) Executing technical and clinical functions as required by the study protocol in accordance with Bioclinica’s GCP’s…
  • 4.5
    Appoint Group – Ilford, England
    14 days ago 14d
    full and independent responsibility for clinical care of patients.- Ability to manage and lead a multi-professional teamQualificatrionsUK… practice- Ability to undertake clinical audit of work and apply findings to clinical work.- Clinical training and experience equivalent…
  • 3.4
    IQVIA Holdings, Inc. – London, England
    30+ days ago 30d+
    and skill in applying, applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International… and 7 years’ clinical research experience including 4 years’ project management experience and experience in clinical operations;…
  • 3.4
    Bioclinica – London, England
    HOT
    Assists Clinical Project Managers in maintaining, reviewing and communicating project progress by: Monitoring internal data flow… (SOPs) Executing technical and clinical functions as required by the study protocol in accordance with Bioclinica’s GCP’s…
  • 4.1
    Zoek – London, England
    11 days ago 11d
    accurate, and that timely data is provided by team members Provide information to the Service Manager on performance and trends… trends in accordance with protocols laid down in relation to quality assurance and performance indicators You will hold a Social…
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