Clinical Pharmacology Director – Home Counties

Jim Gleeson is recruiting for a Director, Translational Medicine & Clinical Pharmacology to join a dynamic,  international pharmaceutical company at their offices in the Home Counties on a permanent basis.

You will be required to lead the early clinical development project team through design, review and analysis of study data and the preparation of final clinical study reports. You will also be responsible for providing strategic development direction and PK/PD, translational/biomarker and clinical expertise spanning late preclinical development through to Proof of Concept.

If you have a PhD in Life Science and extensive clinical research experience, this could be the role for you.

Click here to read the full job description and apply

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Medical Writing Projects Manager – Buckinghamshire

Shreeya Patel is recruiting a Medical Writing Projects Manager to join a pharmaceutical company based in Buckinghamshire on a permanent basis.

The main responsibilities of this role are to plan, organise, and manage medical writing projects in support of global regulatory submissions of drugs and biologics.

As such our client is looking for a individual with significant medical writing experience, including writing clinical study reports, clinical sections of common technical documents, and other formal clinical research documents

For more information on this job or to apply click here

 

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Quality Assurance Manager GCP – Germany

Mylene Paumier is looking for a Quality Assurance Manager GCP to join a biopharmaceutical company at their site in Germany, on a permanent basis.
Responsibilities include:

• Qualitätssicherung klinischer Prüfungen in Phase I-III, Pharmacovigilance-Aktivitäten, sowie klinik-begleitender Biomarker-Programme
• Weiterentwicklung des bestehenden Qualitätssystems im GCP-Bereich entsprechend des Ausbaus der klinischen Forschung
• Unterstützung bei der Erstellung und Umsetzung von SOPs (Standard Operating Procedures) und bei der Entwicklung und Pflege der Qualitätsdokumente

If this is of interest to you click here to read the full job description and apply

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Regulatory Affairs Manager Job – Switzerland

CK Clinical are recruiting for a Regulatory Affairs Manager to join a global pharmaceutical company at their site based in Switzerland.

The main responsibility for this role is to lead  global regulatory projects for the organisation pharmaceutical products, e.g. variations, renewals, new product registrations, labelling changes in assigned markets.

The successful applicant will need to:

  • Fluent in English (written and spoken), German would be a plus
  • Experience in European regulatory affairs

 

Read the full job description here

 

 

 

 

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Health Outcomes Director, Immunoinflammation – London

Jim Gleeson is looking for a Health Outcomes Director, Immunoinflammation for a contract position with a leading blue-chip pharmaceutical company in London.

This role requires the individual to steer reimbursement and access strategy for a number of immunoinflammation assets in early discovery through to full development. Other key responsibilities include ensuring the health outcomes deliverables are of high scientific quality and meet internal and external quality standards.

If you have excellent leadership skills and are interested in this position, click here to read more and apply

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Medical Writing Manager – Berkshire

CK Clinical is recruiting for a Medical Writing Manager to join an international pharmaceutical company in Berkshire on a permanent basis.

The main purpose of your role as Medical Writing Manager will be to ensure that all medical writing documents prepared for assigned Clinical Research Programmes within the company are prepared according to appropriately rigorous, objective and informative medical writing procedures and processes.

In order to be considered for this role, you will need significant experience of medical writing, preferably with experience in oncology or a demonstrated ability to quickly assimilate new therapeutic areas, coupled with prior experience of clinical/preclinical pharmaceutical research and development.

 

Read the full job description here

 

 

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Country Medical Leader Job – South East

CK Clinical recruiting for a Country Medical Leader to join a global pharmaceutical company based in the South East in a permanent office based role.

The over arching purpose of this role is to act as the Medical Directorate strategic lead for all medical activities within a therapeutic area.

This is fantastic opportunity to join a global company in a highly influential role.  Benefits of this role will include:

  • Very competitive salary
  • Company bonus
  • Company benefits

 

Read the full job description and find out more here

 

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Medical Advisor – Neurology

Melanie Miles at CK Clinical is recruiting for a Medical Advisor to join a Global Pharmaceutical Company in a permanent role to be based in Berkshire.

The ideal candidate will have the following qualifications and experience:

  • Medic with GMC registration and with a license to practice, either committed to revalidation or undertaking PMST.
  • The team would consider an R&D or Pharmacovigilance Medic who would like to move into a Commercial role.
  • Pharmaceutical industry experience essential.
  • The job holder will mostly focus on supporting late stage life cycle activities

 

Find more  information about this job here

 

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Medical Science Liaison Scotland & Northern England

Hendre Moolman is recruiting for a Medical Science Liaison to join a company in the pharmaceutical industry in a permanent role in Scotland and Northern England.

As Medical Science Liaison you will be involved providing field-based non-promotional scientific and/or educational support for the UK Respiratory business.

Further responsibilities of this Medical Science Liaison position will require:

  • Ensuring that all activities and interactions are conducted with due regard to all applicable local, global and national laws, regulations, guidelines, codes of conduct, company policies and accepted standards of best practice.
  • Providing field-based medical and scientific support to respond to specific requests from healthcare professionals for further information around company’s Respiratory portfolio or the therapeutic areas.
  • Delivering fair, balanced and unbiased scientific and/or educational presentations reactively (in response to a specific request) to healthcare professionals, either individually or in groups (meetings, and clinical sessions)
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