Job of the Week: Health Economics Senior Manager

We currently have an excellent opportunity for an experienced Health Economics Senior Manager to join one of the world’s leading manufacturers of biosimilar and biopharmaceutical products. This role is based at their site in Uxbridge and will be offered on a 12 month contract at a rate of £69 per hour (PAYE only).

  • The role offers the opportunity to integrate with global research teams and programs, as well as with individual regional and local business units.
  • You will be developing strategies and selection of Patient Reported Outcomes (PROs) for interventional trials and observational studies. You will also develop FDA briefing documents for PRO label discussions.
  • The ideal candidate will have previous pharmaceutical experience as well as extensive Health Economics experience.

Find out more and apply for this role here

 

Posted in Job of the Week, News

Job of the Week: Medical Science Liaison

CK Clinical are currently recruiting for a Medical Science Liaison to join a pharmaceutical company specialising in women’s health. This will be a field based role covering the Midlands and the North of England, therefore travel within this area will be required.

The ideal candidate must have prior experience as a Medical Science Liaison, and it would be beneficial to have therapeutic area experience in women’s health (although this is not essential).

The position provides:

  • A competitive rate/salary dependent on the skills and experience that you can bring to the position.
  • The chance to develop and grow your career working for a long-standing pharmaceutical company that is one of very few in the world offering innovative drugs for women’s gynaecological conditions.
  • A long term opportunity with the potential to become a permanent staff member.

Find out more and apply for this role here

Posted in Job of the Week, News

Job of the Week: Therapeutic Area Lead

We have a great opportunity for a Therapeutic Area Lead to join a major global pharmaceutical company committed to transforming the lives of patients for a better world. This permanent role will be based at their site in Stevenage, with a salary of up to £120K and an excellent benefits package on offer.

The main duties of the role include:

  • Implementing and delivering the clinical operations strategy in the UK.
  • Coaching and leadership of direct and matrix reports.

The ideal candidate should have:

  • A relevant scientific degree.
  • Senior leadership experience within clinical trials.

Find out more and apply for this role here

Posted in Job of the Week, News

Job of the Week: Clinical Trials Manager

CK Clinical are recruiting for an experienced Clinical Trials Manager to join a leading, global pharmaceutical company on a 12 month contract at their site in Marlow. The company is focused on developing, manufacturing and commercialising pharmaceuticals, devices and biological products for patients around the world.

Within the role, you will be responsible for the operational management and execution of GastroIntestinal studies. The ideal candidate will have:

  • Degree preferably in science or a health-related field.
  • Good understanding of GCP and relevant regulations.

Find out more and apply for this role here

Posted in Job of the Week, News

Job of the Week: Clinical Trials Project Manager

CK Clinical have an excellent opportunity for a Clinical Trials Project Manager to join a small but successful Biotech based in Oxford.

The role requires a candidate that can bring a wealth of experience in, and knowledge of, project management of clinical trials within CROs. Experience in Early Phase clinical trials, oncology or other therapy areas would also be ideal.

We have chosen this as our Job of the Week because it offers the following:

  • The chance to join a cutting edge BioTech company about to launch a new and exciting study on its lead cancer vaccine.
  • Great career progression opportunities.
  • Remote working.

Find out more and apply for this role here

Posted in Job of the Week, News

Job of the Week: Regulatory Packaging & Artwork Project Manager

CK Clinical have a wonderful opportunity for a Regulatory Packaging & Artwork Project Manager to join a company in the biopharmaceutical industry. The role is responsible for the initiation of packaging artwork requests and will coordinate across business lines to assure key regulatory timelines are met. The ideal candidate should have a strong previous background in a similar role.

We have chosen this as our Job of the Week as it offers the following:

  • The opportunity to join one of the largest biopharmaceutical companies in the UK, committed to becoming a global leader in life sciences.
  • Paid holidays and a company pension contribution.
  • The chance to develop management skills.

Find out more and apply for this role here

Posted in Job of the Week, News

Four Programmer and Statistician Roles with Specialist CRO

A specialist CRO with an unparalleled reputation for providing high quality analysis and consultancy in the pharmaceutical industry, has a number of permanent Statistician and Programmer roles available at Senior and Principal level. The company is growing but has maintained a family feel, and is committed to providing development opportunities for its employees.

Each of the roles offer great benefits, with regular social events and activities, and memberships to professional organisations. The company is looking to recruit successful candidates as soon as possible, however can wait for notice periods.

There are four available positions:

  • Senior Statistician – Provide statistical analyses and reports on data from a range of projects, clients and therapeutic areas. Specific responsibilities include performing technical and consistency reviews of clinical trials documents and authoring and reviewing simple and complex dataset standards. Find out more and apply here.
  • Principal Statistician – Provide statistical analyses and reports on data from a range of projects, clients and therapeutic areas. Specific responsibilities include providing input into clinical trial documents and presenting study updates internally and at client meetings. Find out more and apply here.
  • Senior Programmer – Provide statistical support across a range of projects, clients and therapeutic areas. Specific responsibilities include performing data checks and data exploration and completing CDISC validation tool reports. Find out more and apply here.
  • Principal Programmer – Provide statistical support across a range of projects, clients and therapeutic areas. Specific responsibilities include leading internal and client study meetings effectively and authoring and reviewing simple and complex study TFL shells. Find out more and apply here.

Contact Stephanie Maccioni for more information on these roles.

Stephanie Maccioni

Stephanie Maccioni

Posted in Job of the Week, News

Job of the Week: PV Specialist

We are looking for a PV Specialist to join a pioneering global medical technology company within the pharmaceutical industry on a 6 month contract. We have chosen this as our job of the week because it offers the following:

  • The opportunity to work in a company that supports healthcare professionals in over 100 countries, with leading positions in Sports Medicine, Wound Management and Orthopaedics Reconstruction to name a few
  • A work location based in Hull. named as the UK’s City of Culture 2017 and easily accessed from the rest of the UK
  • A competitive salary

The role involves supporting the design, development and ongoing commercialisation of pharmaceutical and biological products within the Advanced Wound Management Division. The ideal candidate should have a degree or equivalent in a relevant discipline and good interpersonal skills.

Find out more about this job here

Posted in Job of the Week, News

Technical Regulatory Affairs Manager – Basel

We have an excellent opportunity for a Technical Regulatory Affairs Manager to join a company in the drug discovery industry in Basel. This position is offered on a contract basis between 6 to 12 months. The ideal candidate will execute with following tasks:

  • Write and update the Module 2 (Quality Overall Summary) and the Module 3 (drug substance and drug product quality sections) of the CTD/NDA Applications
  • Create Briefing Books and supportive documentation for Health Authority meetings (pre-IND, pre-NDA, End of Phase II, Scientific Advice meetings)
  • Support and advise the project team regarding pharmaceutical development related to regulatory strategy for submission

If you are interested in this role contact our Swiss Team here or apply here

Find out more here

Posted in Job of the Week, News

Job of the Week: Head of Medical Affairs

We have a wonderful opportunity for a Head of Medical Affairs to join a global pharmaceutical company with an affiliate office in the UK.  This role will lead all medical affairs and medical service and is strategic and operational.

  • Management of 2 MSL’s and 5 head office members across medical information, drug safety and regulatory affair
  • Open to non-signatories and signatories
  •  £90,000+ plus 25% bonus, car allowance, healthcare, dental, life assurance and pension

Find out more and apply here.

 

 

 

Posted in Job of the Week, News