Compliance Consultant - Pharma (Perm or Contract)

Job Ref: J27619
Sector: Clinical
Sub-sector: Pharmaceuticals
Job Type: Permanent
Date Added: 12 July 2018
  • Maidenhead, Berkshire, England, UK
  • £24,000 - £30,000 per Annum
  • Sabrina Andresen
  • 02030964701

Quick Apply

Request a callback

Send To A Friend

Centralisation Team Associate (Compliance Consultant)PharmaMaidenhead, UKContract or Perm, Full-timeSalary: Negotiable, depends on experience

SRG are working in close partnership with a Global Biopharmaceutical Company. Their mission is to develop transformative therapies and medication to change people's lives - recognised in the industry for their cutting edge Science.We are currently looking for someone who has some good grasp of the industry code of practice, great organisational skills and excellent communication/ interpersonal skills.

About the role:

The CT Associate role is pivotal to the success of the In-field team meetings process, reviewing andapproving infield speaker, and sponsored meeting requests, and interactions with HealthcareOrganisations (HCOs) and Healthcare Professionals (HCPs).

To ensure all arrangements and materials are compliant with company policies, standard operating procedures (SOPs) and the Association of British Pharmaceutical Industry (ABPI) Code of Practice.

The CT Associate must work collaboratively with the Infield teams; Brand teams, the Promotional Affairs department, and the Office of Ethics and Compliance department (OEC).

Responsibilities include:

*Work in partnership with Therapy Area (TA) IFT, Brand Team, Promotional Affairs Team and OEC to ensure that commercial objectives can be met whilst also remaining compliant.*Carefully review all TA meetings and interactions with HCPs, HCOs ensuring that all meeting arrangements, content and logistics are compliant with internal policies, SOPs and ABPI Code.*Carefully coordinate and manage logistical meeting arrangements for IFT meetings.*Ensure all meetings records are kept up to date to ensure the audit trail is maintained.*Carry out all responsibilities in accordance with strict internal timelines and internal policy requirements in order to ensure compliance with the ABPI Code of Practice.*Work to ensure effective CT processes and identify and implement opportunities for*development.

Experience and Qualifications required

*University degree/diploma or relevant experience essential*Experience working with the ABPI Code of Practice, or similar, essential*Demonstrated ability using outlook, word, excel and Adobe Acrobat (PDF) to at least a beginner level essential

Desirable Skills (not a must)

*Experience working within Pharma/Medicine/Healthcare industry desirable*Experience managing projects and/or organising meetings/events desirable


For an immediate consideration please press 'apply' now, alternatively contact SABRINA ANDRESENon +44 (0)203 096 4701 and get more information about the role.Our team at SRG Clinical also cover roles in Biometrics, Medical Affairs, Clinical Operations, Medical Information, Pharmacovigilance and Regulatory affairs so do not hesitate to call me at +44 (0)203 096 4701.

Fancy getting rewarded?We find that good people know good people. So when you recommend a friend to SRG and we place them in a contract or permanent job, you could earn a bonus of up to £1,000 of Red Letter Days vouchers as a thank you.

The recruiter has stated that all applicants for this job should be able to prove they are legally entitled to work in the EU/UK. SRG is a trading name of Science Recruitment Group Ltd an Employment Business/Agency.

11/08/2018 15:24:38
GBP 24000.00 24000.00.