Clinical Research Nurse – North East

Russell Oakley is currently recruiting for a Clinical Research Nurse to join a specialist medical device/diagnostic company in the North East on a 12-24 month contract.

You will be working for a company that is aiming to integrate medicines that treat chronic conditions with mobile technology – via their ingestible sensor – to make healthcare more accessible, manageable and innovative.

To apply for this position you should be an RN1 registered nurse with experience of research and of working in secondary care/clinical research environment.

For more information on this clinical job click here

 

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Senior Clinical Program Manager – Cambridge

Russell Oakley is recruiting for a Senior Clinical Program Manager to join a global pharmaceutical company in Cambridge on a permanent basis.

Responsibilities for this role include planning the overall clinical operations strategy, leading multiple cross-functional clinical trial teams and managing the pre-determined clinical budget.

To apply for this position you must have at least 10 years experience of biotech and/or pharmaceutical experienced in human drug development and global drug development.

For more information on this role, or to apply, please click here

 

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Field based Clinical Support Specialist Oxfordshire

Russell Oakley is recruiting for a field based Clinical Support Specialist to join an expanding medical devices biotechnology company based in Oxfordshire.

This company has a unique product that is aimed at the wireless monitoring market and having successfully completed a pilot project is now launching the product globally.

Responsibilities will include providing training to employers and distributors, delivering high standards of customer service and product knowledge whilst participating in focus group and advisory board meetings.

Ideally you will be fluent in French or German, technical competence with patient monitoring equipment and expertise in the care of deteriorating patients.

Click here for more information or to apply

 

 

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Senior Clinical Study Manager Job in London, UK

Russell Oakley at CK Clinical is currently recruiting for a Senior Clinical Study Manager to join a global pharmaceutical manufacturer based in London, UK on a permanent basis.

The company:

This client is a global pharmaceutical manufacturer involved in the development of pharmaceuticals in the therapeutic areas of oncology, diabetes, cardiovascular and hypertension.

Senior Clinical Study Manager Job Description:

As Senior Clinical Study Manager, you will be responsible for  the execution of Phase II and Phase III oncology studies according to ICH guidelines in support of the clinical strategies defined in the Integrated Development Plan (IDP) as they relate to European specific responsibilities. Support of Phase I trials may also be required.

You will be a key member of the oncology clinical team responsible for conducting clinical studies, which includes participating in writing of study protocols; total management of assigned study conduct, including oversight of the study team and CROs/other vendors; identifying and resolving study site issues; managing the study budget and study closeout with a focus on European activities

As Senior Clinical Study Manager, you may also be required to participate in the training of more junior members of staff.

The role will be based in central London but will involve international travel as well as work centred in the UK.

Qualifications, Skills and Experience:

The ideal candidate for this Senior Clinical Study Manager, you will have the following qualifications, skills and experience:

  • Bachelors Degree preferably in Life Sciences, or R.N., or international equivalent.
  • Demonstrable clinical trial management experience including accumulation of one year of monitoring experience required.
  • Demonstrated ability to manage multiple clinical trials on time and within budget.
  • Superior communication skills: written, oral, interpersonal and presentation.
  • Excellent problem solving and analytical skills.
  • Must work effectively in a cross-cultural matrix team environment and be flexible to contribute to the needs of the group.
  • Clear, direct, tactful communication skills are required.
  • Good writing skills with experience in writing study protocols, summaries, clinical brochures, FDA annual reports and other clinical documents for submission to the FDA. Writing should be clear, concise and accurately represent findings.
  • Strategic thinking – Begin to participate in strategic planning. Able to anticipate potential problems and obstacles and plan accordingly.
  • Ability to organize and manage a CRO and multiple sites participating in a clinical trial.
  • Ability to prioritize work effectively to meet timelines.
  • Demonstrates professional and effective presentation skills.
  • Analytical skills – ability to identify study-related, CRO-related or site-related issues, determines the causes and possible solutions to the problem.
  • Responsible for resolving issues with study conduct with appropriate staff, CRO and study sites for a clinical study.
  • Solid judgment is required before applying the solutions program wide.
  • Good judgment, professionalism and independence are needed in interfacing with staff, CROs, study coordinators, and investigators Interpersonal Flexibility – ability to adapt to other personalities and cultural differences, in a respectful manner that is conducive to goal achievement
  • Resource Management – ability to manage internal and external vendor resources related to study trial conduct.

The following skills are not essential but would be desirable for this Senior Clinical Study Manager position:

  • In depth knowledge of oncology clinical trials.
  • Familiarity with MS Outlook, Word, Excel, etc.
  • Participation in NDA/CTD process

How to apply:

Russell Oakley - Senior Consultant at CK Clinical
Please contact Russell for more details.

Click here to apply online now.

For more information regarding this Senior Clinical Study Manager job in London, please contact Russell Oakley at CK Clinical on +44 (0) 114 283 9956 or email roakley@ckscience.co.uk. Please quote reference CL24219 in all correspondence.

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Clinical Imaging Associate Job in Uxbridge

Russell Oakley at CK Clinical is currently recruiting for a Clinical Imaging Associate to join a global drug research and development company based in Uxbridge.

 

As Clinical Imaging Associate you will:

  • Conduct set-up of clinical trials within the internal imaging system under limited supervision
  • Proactively participates in a partnership with the matrix partners
  • Ensure trials are validated before going live
  • Understand financial drivers and their role in decision making
  • Ensures that the conduct of imaging work meets GCP requirements
  • Conduct image review against basic parameters (QC)
  • Raise queries using eDC system or alternative
  • Interact with wider stakeholders, e.g. CROs/vendors (Image Transfer CROs) and monitors.
  • Proactively track timelines and identify issues in order to propose strategies to implement

contingencies and risk planning to meet overall study/program goals.

  • Input into study plans and process documents.
  • Forecast and monitor data volumes within studies and/or across programs
  • Conduct end-of-study learning debriefs for study team
  • Provide input into process improvement initiatives.
  • Identify and disseminate best practices and standardization
  • Assure the quality of the deliverables.
  • Facilitate effective communication and teamwork

 

To be considered for this Clinical Imaging Associate position, you will have:

  • A Bachelors degree or equivalent, major course of study in Science or Health-related preferred
  • 2 years experience in clinical research
  • Strong computer literacy
  • Awareness of GCP and its application to clinical trials
  • Interpersonal skills associated with working in a matrix team
  • Solid understanding of clinical practices.  Understands impact of changes and is able to apply

changes to study design and potentially program level decisions.

How to apply:

Click here to apply online now.

For more information regarding this Clinical Imaging Associate position, please contact Russell Oakley at CK Clinical on +44 (0) 114 283 9956 or email roakley@ckscience.co.uk. Please quote reference CL24004 in all correspondence.

Looking for a new clinical job in the UK? Click here to search our current clinical jobs online now.

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