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Associate Manager Regulatory Affairs Jobs in Cambridge, East of England, England

27 Jobs

  • 3.6
    AstraZeneca – Cambridge, East of England, England
    5 days ago 5d
    company and regional regulatoryaffairs staff to influence developing views/guidance. You will lead the regulatory staff working, provide… equivalent of regulatory drug development including product approval/launch. Expert knowledge of regulatoryaffairs within one or…
  • 3.6
    AstraZeneca – Cambridge, East of England, England
    NEW
    cross-functional projects on behalf of Global RegulatoryAffairs (GRA) when necessary. Provide regulatory leadership as needed in product in-license… equivalent of regulatory drug development including product approval/launch. Expert knowledge of regulatoryaffairs within one or…
  • 4.2
    Vivid Resourcing Ltd – Cambridge, East of England, England
    13 days ago 13d
    creative designs Assist the RegulatoryAffairs and Medical Writing Manager with the provision of regulatory support for clients and… scientific field Minimum of two years' clinical trial regulatoryaffairs experience Fluent written and oral English language…
  • Marketplace Group – Cambridge, East of England, England
    30+ days ago 30d+
    Medical Device Manufacturer requires a RegulatoryAffairsAssociate to assist the regulatory team to ensure compliance of products… surveillance. To assist with registrations and regulatory submissions to regulatory bodies as required. To assist with the legalisation…
  • 3.1
    Gilead Sciences – Cambridge, East of England, England
    14 days ago 14d
    pipeline Gilead’s fast paced Regulatory team in Cambridge is currently looking for RegulatoryAffairsManager CMC. This will focus on… chance to grow your RegulatoryAffairs CMC expertise across a range of territories with diverse regulatory requirements and processes…
  • 3.5
    Mundipharma Research – Cambridge, East of England, England
    14 days ago 14d
    RegulatoryAffairsAssociate (Submission Planning) RegulatoryAffairsAssociate (Einreichungsplanung) Location Cambridge… related to area of expertise with the line manager and/or appropriate RegulatoryAffairs Sub-Team (RAST) members and perform actions…
  • 3.5
    Mundipharma Research – Cambridge, East of England, England
    NEW
    Senior RegulatoryAffairsManager - CMC x2 Senior RegulatoryAffairsManager - CMC x2 Job Introduction . Location… any CMC specific questions from Regulatory Agencies, Associate Companies, other RegulatoryAffairs personnel as required. Assist…
  • 3.1
    Gilead Sciences – Cambridge, East of England, England
    21 days ago 21d
    International RegulatoryAffairs (Respiratory/Inflammation) and will be responsible for the preparation of regulatory submissions… representing RegulatoryAffairs on cross-functional teams. Experience in the preparation/submission of regulatory documentation…
  • 3.5
    Mundipharma Research – Cambridge, East of England, England
    NEW
    RegulatoryAffairsAssociate - Document Management System Support - 12 month STC RegulatoryAffairsAssociate - Dokumenten… appropriate to European RegulatoryAffairs. Work as a team player and perform all reasonable tasks related to regulatory activities in…
  • 4.5
    i-Pharm Consulting Ltd – Cambridge, East of England, England
    NEW
    specific expertise in Clinical Research, Medical Affairs, RegulatoryAffairs, Pharmacovigilance, Quality Assurance and Bioinformatics… activities *Leading campaign reporting *Understanding legal & regulatory compliance and adhering to it on a day to day basis *Travelling…
  • 3.7
    Amgen – United Kingdom
    8 days ago 8d
    role based in RegulatoryAffairs, the Senior Associate will assist in the creation and maintenance of regulatory strategies, submissions… and/or Marketing Applications as well as routine regulatory submissions. Manage IMPD submission and amendments in accordance with…
  • 3.7
    Amgen – United Kingdom
    4 days ago 4d
    CategoryRegulatoryJob Description Title: RegulatoryAffairsManager The company: Amgen is one of the world’s… Communicates regulatory strategies within team Under general supervision, develop predictions for expectations and risks associated with…
  • 3.6
    AstraZeneca – Cambridge, East of England, England
    22 days ago 22d
    Position:Senior Medical Affairs Leader Location: Cambridge, UK / Gaithersburg, USA Salary: Competitive & Excellent Benefits… Main Duties and Responsibilities Overview Global Medical Affairs (GMA) ensures the best patient outcomes by providing healthcare…
  • 3.6
    AstraZeneca UK – Cambridge, East of England, England
    27 days ago 27d
    in the industry. The Regulatory Project Management group sits within the AZ Global RegulatoryAffairs, Patient Safety and QA… experienced AssociateRegulatory Project Directors (ARPD) to join our UK Oncology team. The ARPD is an experienced regulatory specialist…
  • 3.6
    AstraZeneca – Cambridge, East of England, England
    19 days ago 19d
    Global RegulatoryAffairs, Patient Safety and Quality Assurance (GRAPSQA) is a forward-thinking and innovative regulatory, safety… Therefore, you will need to possess a good understanding of regulatoryaffairs to lead and motivate staff and ensure the portfolio is…
  • 3.7
    Amgen – United Kingdom
    24 days ago 24d
    Description Title (Role) RegulatoryAffairs - Senior Manager Organization Global RegulatoryAffairs Group Purpose This… plans and local regulatory requirements. Implements product related regulatory strategies, RegulatoryAffairs processes and activity…
  • 3.7
    Amgen – United Kingdom
    24 days ago 24d
    Description Title (Role) Senior Manager, RegulatoryAffairs Organization Global RegulatoryAffairs Group Purpose This role… plans and local regulatory requirements. Implements product related regulatory strategies, RegulatoryAffairs processes and activity…
  • 3.6
    AstraZeneca – Cambridge, East of England, England
    29 days ago 29d
    Global Medical Affairs (GMA) ensures the best patient outcomes by providing healthcare decision-makers around the world with the… acumen. PRECISION is a multi-faceted, above brand medical affairs-led programme that will advance clinical practice and fundamentally…
  • 4.5
    i-Pharm Consulting Ltd – United Kingdom
    NEW
    specific expertise in Clinical Research, Medical Affairs, RegulatoryAffairs, Pharmacovigilance, Quality Drugsafety/pharmacovigilance… Preparation and review of SOPs *Input into clinical, scientific and regulatory other services provided by the company *PSUR, RMP and PSMF…
  • 3.7
    Pfizer – Cambridge, East of England, England
    NEW
    management in Discovery, Clinical Development, Medical Affairs, Regulatory and other pertinent groups. Participate actively in… with a thorough understanding of the processes associated with clinical and regulatory operations and product defense strategies.…
  • 3.6
    AstraZeneca – Cambridge, East of England, England
    17 days ago 17d
    rheumatoid arthritis. This role of Associate Director, INA Communications, Global Corporate Affairs INA is accountable for building… Medicine Leads, working closely with Global Corporate Affairs corporate affairs colleagues, the regions, key markets and a broad mix…
  • 4.4
    Clovis Oncology, Inc. – Cambridge, East of England, England
    28 days ago 28d
    Leadership, Biostatistics/Data Management, Pharmacovigilance, RegulatoryAffairs, Molecular Diagnostics, Translational Medicine Operations… studies in compliance with companies’ SOPs, regulatory requirements and GCP. Manage and troubleshoot operational challenges, GCP…
  • 3.6
    AstraZeneca – Cambridge, East of England, England
    30+ days ago 30d+
    Medicine Leads, working closely with Global Corporate Affairs corporate affairs colleagues, the regions, key markets and a broad mix… Responsibilities: Accountable for identification of Corporate Affairs priorities within agreed INA and Respiratory portfolios and…
  • 4.5
    i-Pharm Consulting Ltd – United Kingdom
    4 days ago 4d
    specific expertise in Clinical Research, Medical Affairs, RegulatoryAffairs, Pharmacovigilance, Quality Assurance and Bioinformatics… JOB TITLE Clinical Study Manager / Clinical Project Manager / Study Manager / Project Manager / Lead CRA / Principal CRA…
  • 3.1
    Gilead Sciences – Cambridge, East of England, England
    11 days ago 11d
    areas, specifically with Regulatory and IT counterparts, to ensure the needs of the RegulatoryAffairs department are met; Work… development, support, and administration activities for the RegulatoryAffairs SharePoint environment. Provide expertise and oversight…
  • 4.7
    SPD Development Company Ltd – Bedford, England
    23 days ago 23d
    Product Support, Clinical Affairs, Statistics & Data Management, Scientific & Medical Affairs, RegulatoryAffairs, Compliance and Quality… delivery of demo kit into new and existing markets (e.g., regulatory, legal docs, import permits etc.) Support delivery of next…
  • 3.7
    SynteractHCR, Inc. – Ely, England
    16 days ago 16d
    are looking for a dedicated Feasibility Manager to join our Regulatory & Medical Affairs Team in the UK. We offer you a challenging… Research, gather and analyse information on therapeutic areas associated with clinical trial protocols and other relevant information…
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