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Regulatory Affairs Director Jobs in Basingstoke, England

21 Jobs

  • Advanced Regulatory – United Kingdom
    EASY APPLY
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    RegulatoryAffairsDirector - Lead Regulatory Policy for EMEA England - South East On Application Background Regulatory… Regulatory Affairs, Reg Affairs, RA, Regulatory jobs, RA jobs, RegulatoryAffairs Jobs, Lead Regulatory Policy for the EMEA - Regulatory…
  • Advanced Regulatory – United Kingdom
    EASY APPLY
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    Regulatory Affairs, Reg Affairs, RA, Regulatory jobs, RA jobs, RegulatoryAffairs Jobs, RegulatoryAffairsDirector of Policy - Small… East On Application Background RegulatoryAffairsDirector - Lead Regulatory Policy for EMEA Would you consider a…
  • 3.4
    Biogen Idec – Maidenhead, England
    9 days ago 9d
    areas of regulatory science and product development Build and maintain excellent relationships with relevant regulatory agencies… as part of a collaborative regulatory team Actively participate in and contribute to regulatory policy development LI-POT2…
  • 3.6
    PRA Health Sciences – Reading, England
    26 days ago 26d
    OverviewThe Director, Global RegulatoryAffairs provides scientific and related regulatory expertise regarding preclinical and… multiple projects. Provides functional management to the regulatoryaffairs department staff. Responsibilities Provides…
  • Advanced Regulatory – United Kingdom
    EASY APPLY
    NEW
    Regulatory Affairs, Reg Affairs, RA, Regulatory jobs, RA jobs, RegulatoryAffairs Jobs, Regulatory, RegulatoryAffairs, Reg Affairs, RA… RA, Regulatory jobs, RA jobs, RegulatoryAffairs Jobs. Complete the online application or contact for further information quoting…
  • 3.6
    PRA Health Sciences – Reading, England
    26 days ago 26d
    Overview The RegulatoryAffairs Associate (RAA) fulfills the role of Local RegulatoryAffairs Lead (LRAL) and is responsible… providing regulatory input on assigned RFPs, RFIs and BDMs. Contribute to the maintenance and collection of Regulatory Intelligence…
  • 3.6
    PRA Health Sciences – Reading, England
    NEW
    Scientific Affairs-Clinical Pharmacology team within Scientific Affairs of the PRA Business Unit Scientific & Medical Affairs, Safety… medical, commercial and regulatory needs and expectations. Liaises with key opinion leaders and regulatory authorities for the challenge…
  • 3.6
    PRA Health Sciences – Reading, England
    26 days ago 26d
    medical, commercial and regulatory needs and expectations. Liaises with key opinion leaders and regulatory authorities for the challenge… Overview The department of Global Scientific Affairs within PRA Business Unit “Early Development Services (EDS)”is responsible…
  • 3.6
    PRA Health Sciences – Reading, England
    4 days ago 4d
    Because we’re hoping you’re here for the latter. The PRA Medical Affairs team is kind, brilliant and filled with the industry leading… analyses for efficacy and safety, IAE and IASs, dossiers for regulatory submissions for market authorizations of new medicinal products…
  • 3.6
    PRA Health Sciences – Reading, England
    NEW
    Because we’re hoping you’re here for the latter. The PRA Medical Affairs team is kind, brilliant and filled with the industry leading… analyses for efficacy and safety, IAE and IASs, dossiers for regulatory submissions for market authorizations of new medicinal products…
  • 3.2
    Premier Research – Wokingham, England
    4 days ago 4d
    global project team, including Regulatory, Clinical Operations, Biometrics, and Medical Affairs/Safety, to support milestone achievement… so come and be part of it! We’re looking for a Project Director to join our team! This is a permanent role to work in any of…
  • 3.6
    PRA Health Sciences – Reading, England
    26 days ago 26d
    Because we’re hoping you’re here for the latter. The PRA Medical Affairs team is kind, brilliant and filled with the industry leading… analyses for efficacy and safety, IAE and IASs, dossiers for regulatory submissions for market authorizations of new medicinal products…
  • 3.6
    PRA Health Sciences – Reading, England
    19 days ago 19d
    Because we’re hoping you’re here for the latter. The PRA Medical Affairs team is kind, brilliant and filled with the industry leading… analyses for efficacy and safety, IAE and IASs, dossiers for regulatory submissions for market authorizations of new medicinal products…
  • 3.5
    Three – Maidenhead, England
    26 days ago 26d
    This role reports into the General Counsel and RegulatoryAffairsDirector and is responsible for leading the risk and compliance… This role reports into the General Counsel and RegulatoryAffairsDirector and is responsible for leading the risk and compliance…
  • 3.6
    PRA Health Sciences – Reading, England
    26 days ago 26d
    Because we’re hoping you’re here for the latter. The PRA Medical Affairs team is kind, brilliant and filled with the industry leading… analyses for efficacy and safety, IAE and IASs, dossiers for regulatory submissions for market authorizations of new medicinal products…
  • 3.6
    PRA Health Sciences – Reading, England
    26 days ago 26d
    experience Proven experience working within Global RegulatoryAffairs, Regulatory Operations PRA is an EEO/AA employer and is… collaboration with key members from global and local regulatoryaffairs, the GSM will compile and execute submission strategy…
  • 3.0
    BTG plc – Camberley, England
    18 days ago 18d
    Regional Medical Director. Broad Function Reporting directly to the VP, Medical Affairs, the Regional Medical Director will be responsible… in clinical plus non-clinical and/or CMC activities or regulatoryaffairs) ideally in an international matrix environment. Experience…
  • 3.4
    Biogen – Maidenhead, England
    18 days ago 18d
    expert in Emerging Market RegulatoryAffairs and designated region; a. Identify and assess regulatory risks associated with product… the International Regulatory Leadership Team, and represent the Head of Emerging Market RegulatoryAffairs on Management Teams…
  • 3.8
    Alnylam Pharmaceuticals – Maidenhead, England
    30+ days ago 30d+
    to the Senior Director of Patient Advocacy, Medical Affairs based in Cambridge, MA, the EU/Can Associate Director (AD), will be… pharmaceutical or biotech industry, with an understanding of regulatory bodies that impact communications Proven understanding of…
  • 3.4
    Biogen – Maidenhead, England
    18 days ago 18d
    plan in collaboration with EU+ SABR MD, EU Medical Affairs and RegulatoryAffairs for EU+ geographies. Safety content of local labels… works in close collaboration with the product GSO and EU+ RegulatoryAffairs to seamlessly and proactively implement a strategic program…
  • 3.4
    Biogen Idec – Maidenhead, England
    30+ days ago 30d+
    plan in collaboration with EU+ SABR MD, EU Medical Affairs and RegulatoryAffairs for EU+ geographies. Safety content of local labels… works in close collaboration with the product GSO and EU+ RegulatoryAffairs to seamlessly and proactively implement a strategic program…
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