Final Signatory - Medical Advisor

Final Signatory - Medical Advisor
  • Competitive
    ANNUM
  • Temporary
  • Brentford, London, England, UK Brentford London UK TW8 9GS
Job Ref: J2160526
Sector: Clinical
Sub-sector: Pharmaceuticals
Date Added: 27 May 2021
Final Signatory - Medical Advisor - Brentford

Job Title: Final Signatory - Medical Advisor Location: Brentford (Remote)Contract: Temporary

SRG are working with a global pharmaceutical company to help them find a motivated experienced Medical Advsior (Final Signatory) to join our team.

Responsibilities:

* Responsible for the successful timely completion of compliant review, approval and certification of the majority of UK Pharma Promotional and Non-promotional materials, activities and meetings in line with ABPI.* Work with relevant cross-functional stakeholders to establish a uniform approval excellence approach across commercial and medical teams aiming to constantly identify needs leading to continuous improvement and enhancement of the process.* Extensive cross-matrix integration with multiple teams across all therapy areas* Work with teams supporting decision making through supplying governance and compliance expertise enabling appropriate activity selection and seeing these through to compliant implementation.* Successfully manage and resolve approval issues, managing conflict where required with project owners and counter signatories.* Responsible for reliable and regular participation at compliance accountability meetings and ensuring all other necessary specialist inputs are incorporated as required.* Responsible for generating good project team working spirit to support the planning, coordination and implementation of activities and stakeholders.* Responsible for the day-to-day management and completion of agreed deliverables on time and within the agreed scope. Monitors, controls and reports on project progress on a regular basis and when exceptional circumstances arise* Continuously maintains self-signatory status and keeps an up-to-date knowledge of all relevant laws, regulations, codes, policies and SOPs.* Participate in writing, training and maintaining SOPs related to constantly enhance and improve the in-house approval process* Performs self-inspection and related management monitoring activates as and when needed * Generation and communication of copy approval metrics to ensure UK compliance and share best practice.* Responsible for the institution and upkeep of the CAT team files, meetings records and correspondence

Requirements:

* UK Registered Pharmacist (Pharmacists must hold an up to date registration with the General Pharmaceutical Council (GPhC) and be actively undertaking continual professional development (CPD) assessed by the GPhC)* GMC Registered Doctor* Extensive final Medical signatory copy approval knowledge/experience in the pharmaceutical industry* Strong familiarity with and confidence in the ABPI Code of Practice and its application* Strong familiarity with and confidence in implementing compliance frameworks* Experience of using Veeva Content Lab or similar/other copy approval systems* Therapy knowledge in one or more of the following therapeutic areas: Respiratory, Vaccines, Metabolic, Central Nervous System/AnaesthesiaTo apply click the link or send your CV to thomas.ramsay@srgtalent.com

Key words: ABPI / Pharmacists / GMC / Respiratory / Medical / GPhC / CPD / Pharmacology / Pharmacy

SRGTalent
26/06/2021 10:45:08
GBP 0.00 0.00 Annum
Contact Consultant:
Thomas Ramsay

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