Clinical Regulatory Documents Associate Jobs in United Kingdom | Glassdoor

Clinical Regulatory Documents Associate Jobs in United Kingdom

231 Jobs
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  • 4.4
    ProClinical Ltd – United Kingdom
    4 days ago 4d
    components of regulatory documents such as Investigator brochures updates (IBs),. * Facilitate construction of non-clinical documentation… of a repository of modular nonclinical regulatory documentation stored within a document management system for the purpose of generating…
  • 3.5
    AstraZeneca – Cambridge, East of England, England
    11 days ago 11d
    , and document management utilizing the support and input of Global Regulatory Operations, Marketing Companies, Clinical Research… /or region Review documents and provide regulatory input (e.g., response documents, high level documents, study protocols, PSRs…
  • 3.6
    AbbVie – Maidenhead, England
    23 days ago 23d
    The Associate Director of the Clinical Trials Regulatory Group (CTRG) provides Strategic Global Regulatory Leadership for Clinical… industry in global regulatory or an associated area Ideally experience in global clinical trial regulatory affairs with knowledge…
  • 3.7
    Amgen – United Kingdom
    1 days ago 17hr
    collection of functional documents in support of regulatory applications Coordinate QC of regulatory documentation (e.g. briefing packages… assistance with, the creation and submission of regulatory documents, and may be the regulatory lead for a program under the supervision…
  • 4.0
    Johnson & Johnson – High Wycombe, England
    20 days ago 20d
    EMEA REGULATORY AFFAIRS ASSOCIATE RMC SPECIALIST JANSSEN LOCATION: HIGH WYCOMBE CLOSING DATE: Wednesday 26th April Are you… departments. The responsibility of the EMEA Regulatory Affairs Associate is to work with the RMC Professionals and LOC respective…
  • Hydrogen International Ltd – Boston, England
    4 days ago 4d
    execution of global regulatory activities and submissions. * Provide support on both clinical/non-clinical aspects of drug development… Associate Director Regulatory Affairs- Boston, Massachusetts USA Level: Associate Director TA: Oncology or Immuno-Oncology…
  • 2.8
    Covance – London, England
    25 days ago 25d
    Posting Title Clinical Research Associates - All Levels Requisition ID 67420BR Job Category Clinical Research Associate Locations… are always looking for talented clinical research professionals for Clinical Research Associate positions (CRA) in the UK. If you…
  • PE Global – Uxbridge, England
    22 days ago 22d
    creation and submission of regulatory documents and may be the regulatory lead for a program under the supervision of a more experienced… collaboration with Regional Regulatory Lead Create and maintain product regulatory history documents through IMR/rRISE and appropriately…
  • 3.4
    Celgene Corporation – Hillingdon, England
    1 days ago 23hr
    cross-product submission plan in association with Global/Regional Regulatory Lead, Regulatory CMC, commercial, affiliates &/or… holders in a timely manner. • Ensures that copies of regulatory documents are archived appropriately • Can identify when to escalate…
  • 3.7
    Amgen – Uxbridge, England
    1 days ago 17hr
    national legislation and regulatory requirements. Provides content guidance for regional regulatory documents and meetings in accordance… Strategy and Execution Plans and manages regulatory submissions (e.g. clinical trial and marketing applications) for products…
  • 5.0
    Paramount Recruitment Ltd – Welwyn Garden City, England
    10 days ago 10d
    working within clinical research or healthcare and at least 2 years experience of working as a clinical research associate. You should… and managing study documentation,tracking and reporting study metrics as well as clinical and non-clinical supplies. Preparing…
  • 3.7
    Amgen – United Kingdom
    Today 5hr
    national legislation and regulatory requirements. Provides content guidance for regional regulatory documents and meetings in accordance… Strategy and Execution Plans and manages regulatory submissions (e.g. clinical trial and marketing applications) for products…
  • 3.9
    S E C Recruitment Limited – Bury St Edmunds, England
    2 days ago 2d
    Car allowances. The Clinical Research Associate conducts site monitoring responsibilities for Clinical trials, according to Standard… submissions, notifications to regulatory authorities, translation of study-related documentation, organization of meetings and…
  • 2.8
    United BioSource – United Kingdom
    2 days ago 2d
    degree in life sciences desirable Relevant regulatory / clinical research document management experience in a pharmaceutical company… role is the creation of regulatory documents and development of regulatory strategy to achieve regulatory approvals and clearances…
  • 3.3
    PSI CRO UK LIMITED – United Kingdom
    26 days ago 26d
    Support to Regulatory Affairs in procurement of site regulatory documents - Maintenance of appropriate documentation regarding… we are expanding the PSI Clinical Operations department and looking for a Clinical Research Associate II to join our highly professional…
  • 5.0
    Paramount Recruitment – Welwyn Garden City, England
    9 days ago 9d
    working within clinical research or healthcare and at least 2 years experience of working as a clinical research associate. You should… and managing study documentation,tracking and reporting study metrics as well as clinical and non-clinical supplies. Preparing…
  • Technical Placements – Farnham, South East England, England
    25 days ago 25d
    We are seeking a CRA - Clinical Research Associate with experience of monitoring Clinical Trials. Salary is negotiable and depends… in-house clinical research as well as multi-site clinical trials, they have a thorough understanding of all aspects of clinical trials…
  • 3.0
    Mapi – United Kingdom
    6 days ago 6d
    physicians, regulatory authorities and health care technology purchasers. Job Title: Associate Director, Regulatory Affairs CMC… The Associate Director, Regulatory Affairs CMC authors’ chemistry, manufacturing and controls (CMC) portions of regulatory submission…
  • 3.5
    AstraZeneca – Cambridge, East of England, England
    9 days ago 9d
    delivery of a study and its regulatory documents through finalization of the protocol through to the Clinical Study Report (CSR) and… Study Management Associate within Early Clinical Development. The Study Management sits within the Early Clinical Development (…
  • Your JobsPortals – Slough, Berkshire, South East England, England
    1 days ago 17hr
    , CRA, Clinical Research Associate, Clinical Monitoring Associate, Clinical Monitor, Clinical trial associate, Clinical Project… into Clinical, Regulatory and Data management teams within CRO's, Pharmaceutical, Generic and Biotech companies. Associated keywords…
  • Stem CentRx – Maidenhead, England
    23 days ago 23d
    industry in global regulatory or an associated area Ideally experience in global clinical trial regulatory affairs with knowledge… The Associate Director of the Clinical Trials Regulatory Group (CTRG) provides Strategic Global Regulatory Leadership for Clinical…
  • 3.5
    AstraZeneca – Cambridge, East of England, England
    3 days ago 3d
    Early Clinical Development Salary: Competitive Location: Cambridge, UK / Gothenburg, Sweden AstraZenecas Early Clinical Biometrics… talented SAS programmers to join their Clinical Trial Data Science group. Early Clinical Biometrics is totally focused on delivering…
  • 5.0
    Harris Lord Group – Horsham, England
    30+ days ago 30d+
    of European Regulatory departments Key words CTAA, clinical, trials, data, record, SAE, RA Officer, regulatory, affairs, investigator… least 6 months of industry experience in a regulatory environment Experience in clinical trial applications within EU regions highly…
  • Caligor Rx – Dartford, England
    24 days ago 24d
    ’ pharmaceutical industry global clinical trials experience working as a regulatory associate, or similar, with a Life Science… JOB DESCRIPTION: Senior Regulatory Access Associate Summary of Job Purpose and Person Specification Caligor is a trusted…
  • 4.0
    Park Street People – Uxbridge, England
    18 days ago 18d
    initially be a 12 month contract. As a Senior Clinical Research Associate you will have full monitoring responsibilities across… correct dispensing Attend investigator meetings Liaise with Regulatory Affairs dept for submissions and changes Key Skills…
  • 2.4
    Pharm-Olam International – Ascot, England
    3 days ago 3d
    are conducting clinical trials in accordance with international Regulatory and Ethical guidelines for Good Clinical Practices (GCP… procedures for documentation of feasibilities performed. Identifies the documentation required for review by Regulatory Authorities…
  • 2.4
    Pharm-Olam International – Ascot, England
    4 days ago 4d
    contact for the clinical team for designated project communications, correspondence, and associated documentation. Performs administrative… that the clinical trial is conducted in accordance with international regulatory and ethical guidelines for Good Clinical Practice…
  • 2.8
    Covance – Leeds, England
    10 days ago 10d
    and coaching in DM related clinical trial processes, department technical capabilities, and associated turnaround durations. •Ensuring… Having input in writing, reviewing and updating SOPs and associated documents as required. •Performing QC on all aspects of work performed…
  • 3.3
    NHS Jobs – United Kingdom
    1 days ago 13hr
    Compliance and Clinical Effectiveness Manager in the delivery of all areas of compliance with regulatory requirements and clinical effectiveness… key documentation and maintain up to date and accurate records. Facilitate the collection of Trust compliance and clinical effectiveness…
  • 3.7
    Regeneron – London, England
    3 days ago 3d
    study timeline Preparation of Study Documentation • Reviews essential regulatory documents • Establishes and oversees risk management… ) to deliver clinical research studies on time, within budget and with good quality in compliance with Regulatory Authorities regulations…
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