An experienced industry medic is required for this 12 month contract role where you will be accountable for patient safety and provide medical guidance during study design and execution.

In addition to study level activities, you will participate in standing committees such as CRC, review compounds for potential in-licensing including performance of due diligence reviews and provide assistance to New Business Development on Market Opportunity and Target Product Profile.

To find out more, please contact Ben Traies at CK Medics on 01438 743 047 or email btraies@ckmedics.com.

In this new role to the business you will provide medical and scientific input in the development of Inflammation/Biologics projects at various stages of development with the aim to achieve fast regulatory approval of new chemical entities according to corporate strategy.

To be considered for this Senior Director position, you will be medically qualified with full GMC registration, preferably a PhD also. You will have demonstrable experience in inflammation and/or biologics and be building a sound reputation within this field with a robust publication record to underline this.

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For more information, or to apply for this Senior Director position, please contact Ben Traies on 01438 743 047 or email brtraies@ckmedics.com

Alternatively, click here to apply for this Senior Director position online now.

Working with the Head of Pharmacovigilance, as Senior Medical Advisor you will be responsible for the provision of a comprehensive Pharmacovigilance and Drug Safety service to European and Global; stakeholders.

Our client has a team of Drug Safety Medics. Whilst this role is not a management role within the department it is an ideal opportunity for a candidate with more experience to take on a leadership and mentoring position to other less experienced Pharmacovigilance medics and help them with their development.

The key responsibilities of this Senior Medical Advisor role will include:

• To proactively manage the global safety aspects for a specific product, or group of products.
• To be a member of the body that manages pharmacovigilance globally.
• To support the Head of Product Safety and the Qualified Person for Pharmacovigilance (QPPV) in the collection, assessment, evaluation, distribution and reporting of individual and cumulative safety reports.
• As the senior member of the team provide orientation, training and support, and to assist the Head of Product Safety in the maintenance of standards of performance.
• To lead the response to safety-related medical queries from regulatory authorities, external bodies and internally for specified products.
• Be responsible for a leading safety evaluation, including signal detection and benefit-risk analysis.

This opportunity is a rare one to join an established and forward thinking safety department under the stewardship of one of the industries most respected and experienced heads. 

In order to be considered for this Senior Medical Advisor position, the key qualifications and qualities you will possess will include,

• Experience as a Pharmacovigilance medic
• GMC registration
• A “can do” attitude with a genuine team focus
• Outstanding communication skills
• Tact, Diplomacy and an eye for detail

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For a full job description or to discuss the role further, please contact Ben Traies on 01438 870021 or email btraies@ckmedics.com.

As Senior Medical Advisor will provide medical and scientific support for the marketing and sales of relevant therapeutic unit products by:

• Provision of expert medical and scientific advice on these products and related disease areas.
• Contact with opinion leaders and other health professional in the relevant therapeutic area.
• Medical and scientific input into marketing and sales strategy for these products.

In addition to this you will manage the day-to-day activities of the Medical Information Unit and be an expert on the ABPI and IPHA Codes of Practice to ensure and monitor company compliance with The Codes and other policies.

In order to be considered for this Senior Medical Advisor role you will have the following qualifications and experience:

• Preferably minimum of 5 years experience of medical advisor in the UK (ideally cardiovascular)
• Able to work in and adapt to a medium sized pharmaceutical company
• Authorised as Final Signatory
• GMC registered
• Excellent understanding of the ABPI and IPHA CoP
• Proven people management experience – already being responsible for a MIU

This is a 12 month contract covering maternity leave so its essential that you have the ability to at the end of September.

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If you are interested in finding out more about this Senior Medical Advisor role please contact Ben Traies on 01438 870021 or email btraies@ckmedics.com

Alternatively, click here to apply for this Senior Medical Advisor role online now.

We are currently working with an experienced and talented GMC registered Medic seeking work on an interim or contract basis.

This candidate has recently completed a role as Medial Director where he was responsible for a range of Therapy areas across the European region. He has experience as an Clinical Research Physician and Pharmacovigialnce medic but has particularly strong expertise within Medical Affairs.

He currently has availability for 3 to 5 days a week and is able to start work immediately. If you have an immediate need for an enthusiastic medic with EU and Global expertise, please get in touch with me at jhartsmith@ckmedics.com.

Reporting to Country Lead, as Contracts Specialist you will be responsible for working with Local and European Medical Affairs personnel and clinical trial managers to prepare and oversee all contracts for investigational initiated studies within the UK.

This role is key to ensuring that all studies are delivered according to global and regional quality and safety SOPs for single country studies.

Key responsibilities of this Contracts Specialist role will include:

- Investigator sponsor liaison from project concept through to report and /or publication

- Collaborating cross-pharma (Medical Affairs both local operating company and EMEA

- Management of IMP distribution, tracking of trial supplies, including assessment and development of supply chain specifically for the individual studies and product, and coordination of IMP labelling and QP release

-  Negotiate Research Funding Agreement with Investigator Sponsor

- Budget forecasting, management and reporting

- Study tracking, information management and reporting,

- Establish safety reporting plan, taking into account R&D partner and regulatory status of product safety updates

- Overseeing vendors and contractual obligations.

- Participate and facilitate in internal review committees

- Ensure regular reporting and updates to all key stakeholders

The ideal candidate for this Contracts Specialist role will have demonstrable experience in the Pharma industry in clinical trials with high level of knowledge of UK specific clinical trials infrastructure and contracting with established and emerging research networks.

Apply now

For more information, or to apply for this Contracts Specialist job now, please contact Ben Traies on 01438 870021 or email btraies@ckclinical.co.uk.

Alternatively, click here to apply online for this Contract Specialist job now.

As Clinical Trials Assistant, you will be responsible for the co-ordination and support of high quality Clinical Trials and projects, ensuring standardisation and consistency of delivery across studies in accordance with current best practices: meeting the requirements of the specific brand strategy and thereby supporting the UK Pharma business.

Further responsibilities of this Clinical Trials Assistant job will include:

• To drive effective Drug Supply for clinical studies by appropriate forecasting, tracking and maintenance
• To provide co-ordination and support to CPM, LCPM and Clinical Project Group, in order to meet the business needs
• To develop, maintain and manage appropriate study documentation in line with guidance including ICH-GCP, local and global SOPs and current best practice
• To set up, track and maintain study information and to report internally and externally on study progress
• To drive and track the Expression of Interest process according to SOP
• To contribute to Clinical Project Group efficiency and process improvement, including contributing to the development of best practices and appropriate tracking tools and templates
• To manage stand-alone projects as required by LCPM eg IPS or Compassionate Use Programmes

To be considered for this Clinical Trials Assistant job, you will have a Life sciences degree or nursing equivalent combined with experience in Clinical Trial environment and a broad based knowledge of the clinical trial process. Familiarity with clinical trial regulatory and ethical requirements is also essential

Apply now

If you are interested in this Clinical Trials Assistant position please contact Ben Traies on 01438 870021 or email btraies@ckclinical.co.uk

Alternatively, click here to apply for this Clinical Trials Assistant job online now.

In this commercially focused Clinical Project Manager role you will be responsible for the planning, implementation and follow-up of high quality Clinical Trials and projects in partnership with Marketing function, in order to meet the requirements of the specific brand strategy and thereby supporting the UK pharmaceutical business.

Further responsibilities of this Clinical Project Manager job include:

• To integrate with Marketing/ Medics in identifying clinical project strategy in order to maximise marketing opportunity of brand
• To lead local Study Management Team in planning implementation of clinical trials, ensuring documentation and communication of plan
• To lead local Study Management Team in implementation of clinical trials, ensuring the studies are performed and conducted in compliance with ICH-GCP guidelines, SOPs, local operating guidelines and all applicable regulatory requirements 
• To provide complete follow-up for clinical trials
• To provide the day-to-day operational management of CROs and vendors ensuring delivery against contracted scope of work

To be considered for this Clinical Project Manager role, you will be an experienced clinical project manager with a strong background in oncology coupled with the ability to join the department and hit the ground running.

Apply now

If you are interested in this Clinical Project Manager role please contact Ben Traies on 01438 870021 or email btraies@ckclinical.co.uk.

Alternatively, click here to apply for this Clinical Project Manager job online now.

The main focus of this Safety Operations Physician job will include liaising with the four regional centres across the globe to manage workloads and ensure that ICSRs and medical reviews are conducted in adherence with the company’s internal standard operating procedures.

Your input will also be important in agreeing on the objectives for Operations Physicians and in order to set targets that meet pharmacovigilance requirements you should have good knowledge of US and EU regulations in this field.

The ideal candidate for this Safety Operations Physician job will be educated to an MBBS or equivalent medical degree recognized in the EU is essential. Furthermore a qualification such as a Diploma in Pharmaceutical Medicine would be beneficial. You should have had experience in Pharmacovigilance and training for management and in addition you must be flexible, motivated and willing to travel.

As Safety Operations Physician, you will have the ability to undertake detailed analysis and evaluation of scientific data and give concise and accurate reports will be among your talents, whilst your confidence and communication skills will allow you to influence, negotiate with and present to the Head of the Regional Centre.

This is a first rate opportunity that offers you to utilise your medical knowledge and pharmacovigilance expertise in their global network of safety Operations Physicians. In order to deliver compliance and high quality medical reviews and ICSRs a blend of a high level academic achievement in medicine, pharmaceutical knowledge and effective management ability is required.

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For more information, or to apply for this Safety Operations Physician job, please contact Ben Traies on 01438 870021 or email btraies@ckmedics.com.

Alternatively, click here to apply for this Safety Operations Physician job online now.

• Salary upwards of £80K plus excellent annual bonus and company benefits

As Medical Manager you will lead the Medical Affairs Team in the Diabetes, Cardiovascular Disease and Thrombosis business, and support the organisations wide portfolio of products.

The main focus of this Medical Manager role will be to manage and mentor the team of medical advisers – working with them to ensure that the medical activities generate the best commercial results whilst complying with all regulations and guidelines.

As Medical Manager, you will feed your knowledge, experience and insight into the business so that everything from clinical trials and submissions, to pharmacovigilance and regulatory affairs generates the best possible commercial results. You will also take responsibility for the clinical trial programme, leading the team as they draft protocols, initiate studies, supervise trials and maximise their outputs. Working as Medical Manager your expertise and informed opinions will also influence the development of partnership opportunities.

The ideal candidate for this Medical Manager job will have significant Medical Affairs experience to add to a solid clinical career. You must be a UK registered medical practitioner, ideally with a higher medical qualification. Therapeutic experience would be beneficial, but the flexibility to rapidly acquire and utilise new knowledge is even more important. Your Diploma of Pharmaceutical Medicine would place you at an advantage, as would holding (or working towards) a CCT in Pharmaceutical Medicine. Your Medical Affairs experience will have given you excellent insight into the current workings and challenges faced by the NHS. You’ll also bring a successful track record of delivering clinical trials, and positive interactions with national HTA bodies.

This Medical Manager position also demands a highly organised, commercially aware candidate who is focused on results. As Medical Manager you’ll also be the kind of person who can forge strong, productive relationships across and outside of the organisation.

Apply Now

For more information or to apply for this Medical Manager job, please contact Ben Traies at CK Medics on 01438 870021 or email btraies@ckmedics.com.