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Hendre Moolman is recruiting for a Senior Medical Affairs Officer to join a leading Pharmaceutical company based in Surrey.
Senior Medical Affairs Officer Job Description:
As Senior Medical Affairs Officer, you will be responsible for the provision of a medical information service to internal customers and to external contacts. You will also support the sales, marketing and regulatory teams in United Kingdom by providing medical evaluation and information in all activities to ensure targets are met and to ensure compliance. Additional responsibilities include providing back up for drug safety activities.
Further responsibilities of this Senior Medical Affairs Officer role include:
Accountable for the effective management and continuous development of UK Medical Information service.
Represent the UK in global Medical Affairs network (OTC).
Develop and maintain medical and scientific awareness of the Consumer Health product portfolio and disseminate information to internal customers.
Provide medical advice to support sales, marketing, and other internal departments including medical input to claims development and creative approvals and expert input to data and literature evaluation, making clear to the business the impact of any findings.
Ensure compliance with the relevant Codes of Practice in relation to promotional materials.
Act as internal and/or authorised ABPI signatory for promotional materials as appropriate.
Provide medical input into local PR, including review and adaptation of global PR to local needs/regulations, under the internal quality control procedures.
Support marketing in development of customer focused claims as well as monitoring/challenging claims made by competitors.
Support the local Sales and Marketing teams, producing high quality briefing and training materials and development of brands promotional and communication material.
Produce, update and approve prescribing information in a timely fashion and in line with relevant regulations.
Co-ordinate and implement timely updating of product entries in external databases, compendia and journals.
Act as company administrator for eMC and NHS prescription systems.
Advise on medical issues relating to advertising copy, patient information leaflets, summary of product characteristics, etc.
Process Drug Safety cases and perform follow up activities as required.
Be a member of the UK signal detection team.
Scientific evaluation of new claims and line extension possibilities presented by Global Drug Regulatory Affairs or Marketing on existing portfolio.
Scientific evaluation on feasibility of New Project Development presented by Global Drug Regulatory Affairs or Marketing.
Interface with the medical and healthcare community.
Develop and maintain contacts with Specialists in appropriate fields and Trade Associations to further the interests of NCH.
Sales force training and support across UK and ROI region.
Assist with the training of colleagues in the medical aspects of our business.
Provide company wide training in the applicable Code(s) of Practice.
Qualifications, skills and experience:
BSc in relevant subject or pharmacist
Proficiency in analysing scientific data and drawing the relevant conclusions
Proficiency in communication skills, how to explain complicated matters in a simple way
For more information regarding this Senior Medical Affairs Officer position, please contact Hendre Moolman at CK Clinical on 01438 870 023 or email email@example.com. Please quote reference CL23455 in all correspondence.
An exciting opportunity as Senior Compliance Executive has arisen to join an established pharmaceutical company in Buckinghamshire, UK.
In this Senior Compliance Executive position you will contribute towards developing, implementing and maintaining company policies and procedures covering activities governed by the ABPI Code of Practice for the Pharmaceutical Industry. You will provide central guidance and training on the ABPI Code of Practice and oversee and manage the Zinc MAPS system for promotional materials
Develop, manage and implement company policies and procedures to meet statutory, quality and business requirements for all aspects of promotional activity.
Train employees on company procedures for promotional activities and the ABPI Code of Practice.
Oversee and manage all aspects of the Zinc MAPS system both internally and externally.
Develop and manage a central repository for promotional job bags.
Maintain register of company signatories and a current awareness of legislation and regulations governing promotional activities in the pharmaceutical arena, in addition to Code of Practice updates and cases.
Code of Practice and regulatory check of Company promotional material (when assigned).
Qualifications & Experience:
Degree in Life Sciences, Pharmacy or equivalent experience.
A high level of experience with the ABPI Code of Practice and Advertising regulations is essential for this role, as is knowledge and understanding of the pharmaceutical industry particularly commercial, regulatory and information functions.
Excellent organisational and team working skills.
Proactive with strong communication skills and ability to work to tight deadlines in pressured environment.
Ideally familiar with Zinc MAPs and IT systems such as Word, Excel, PowerPoint and Lotus notes.
For more information or to apply for this Senior Compliance Executive position, please contact Hendre at CK Clinical on +44 (0)1438 870 023 or firstname.lastname@example.org quoting 21169 to make us aware of your interest.
GCP Manager needed for a leading healthcare charity based in London, UK.
Reporting to the Head of Quality, Regulatory and Pharmacovigilance, as GCP Manager you will be required to take responsibility of all aspects of GxP within the organisation.
The main focus of this GCP Manager job will be to oversee the GCP programme (for Phase I & II studies), though you will also oversee GCLP for a number of laboratories and GMP for two manufacturing sites.
The successful candidate for this GCP Manager position will be educated to a minimum BSc in a relevant technical subject and will hold the following skills and competencies:
Extensive Quality Assurance experience gained within the Clinical Trials arena
Experience of the management and implementation of QA and QC systems
Experience of the conduct or organisation of audits
Good line management capability
For further information, or to apply for this GCP Manager job, please contact Jim Gleeson on 01438 870027 or email email@example.com.
This year, the DIA (Drug Information Association) chose Monaco and its state-of-the-art Grimaldi Forum to hold it’s 22nd Annual EuroMeeting, and CK Clinical had the pleasure of attending.
The DIA Annual EuroMeeting is the largest event of its kind in Europe. From the 8-10th March 2010, 3,000 professionals from biopharmaceutical industry, contract service organisations, academic research centres, regulatory agencies, health ministries, patient organisations and trade associations, descended on Monaco.
CK Clinical’s first visit to the DIA Conference was a resounding success. Pharmaceutical jobs were brought in across all sectors, and the conference definitely acted as a brilliant springboard kick off our campaign to enter the European market.
We also ran a prize draw to win an Apple iPod Touch, the winner being a Departmental Manager from Novo Nordisk in Denmark. Thank you to everybody that entered.
The Grimaldi Forum was an impressive waterfront venue, filled with daylight and a stunning glass entrance. A perfect venue to network with clients. Monaco was incredible with Ferrari’s, Mercedes Benz and Bentleys everywhere you looked. The hotel even had its own helipad!
We are very much looking forward to attending and exhibiting at next year’s DIA Conference in Geneva.