Medical Science Liaison

Hendre Moolman is recruiting for a Medical Science Liaison to join a leading pharmaceutical company in the south and south west.

The role will be field based and focused on the Oncological and Immunological sectors. You will be supporting healthcare professionals in a scientific and medical capacity, responding to requests in regards to the specialised areas.

A PhD, Masters or Pharmacist qualification is needed, as is relevant experience in the medical or pharmaceutical industries.

For more information, please click here

 

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Medical Manager Job in Hertfordshire

Hendre Moolman is recruiting for a Medical Manager to join a successful Pharmaceutical company based in Hertfordshire. This is a 12 month fixed contract position.

Medical Manager Job Description:

As Medical Manager, you work as part of the Medical Affairs team on a selected product area. Your work will include, but will not be limited to the following:

  • Developing and implementing clinical trial plans
  • Supporting the brand teams with technical expertise
  • Interpreting data for promotional activities and providing other medical support to maximise the company’s potential.

Further responsibilities of this Medical Manager position will include:

  • Responsibility for medical education program and support key pre-launch activities for new medicine
  • Creating and developing of publications, educational symposia, internal and external educational materials, with support to advisory boards, and clinician interactions
  • Researching, collating, presenting and offering expert opinion on scientific, medical and regulatory information to support both internal and external customers
  • Identify and develop strong, sustainable relationships with external Opinion Leaders to deliver both opportunity and provision to execute the product strategy
  • Developing, designing or advising on clinical trial programmes and strategic clinical issues, maximising the marketing/selling opportunity of the product at both a local and International level and ensure subsequent publications of appropriate clinical data to support portfolio
  • Managing the integrity and accuracy of scientific, medical and regulatory data communicated both internally and externally for both promotional and non-promotional purposes, including delivering appropriate training, in order to enhance the company reputation
  • Acting in expert capacity for all media, Public Affairs and external organisations requests
  • Ensuring adherence to ABPI code of practice in terms of promotional materials, behaviour and attitudes

 

As Medical Manager, you will have the following qualifications, experience or skills:

  • Post graduate qualification in Life Sciences or equivalent (e.g. PhD, MSc) or degree and specific experience for job and/or
  • Medical Degree (MBBS) or similar.
  • Pharmacist
  • Sound understanding of the ABPI Code of Practice
  • Relevant Pharmaceutical industry experience
  • Knowledge of Cardiovascular medicine
  • Experienced in presenting, data analysis and statistics, team work and communication
  • Proven track record in developing medical education programs
  • Established customer relationships within cardiovascular

 

How to apply:

Click here to apply online now.

For more information or to apply for this Medical Manager position, please contact Hendre Moolman on 01438 870 023 or email hmoolman@ckclinical.co.uk. Please quote reference 23641 in all correspondence.

Click here to search our pharmaceutical jobs in Hertfordshire now.

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Safety Risk Lead Jobs in Kent

Hendre Moolman at CK Clinical is currently recruiting for a number of Safety Risk Lead jobs with a Pharmaceutical company in Kent.

Working on a contract basis, as a Safety Risk Lead, you will performing proactive Safety Surveillance and Risk Management to effect product safety signal detection and evaluation, risk assessment and safety risk minimisation.

Key responsibilities of this Safety Risk Lead include:

  • Safety Risk Leads (SRL) in Safety Surveillance and Risk Management (SSRM) will be the product “safety-management-team”, flexibly supporting all business units.
  • Collaborate closely with the relevant Worldwide Safety Strategy VP Safety Strategy Business Unit/Research Unit Leads to support the appropriate BU safety strategies
  • Provide and accumulate specific pharmacovigilance expertise, and applying this to various Business Units products assigned to the SRL 
  • Perform proactive Holistic Safety Review for products, across the span of relevant available safety data information.
  • Reviews are incremental, cumulative and aggregate, to include the body of safety information
  • Ensure Consistency of Safety Risk Messaging for a particular product or class of products, across multiple indications within the many safety reports and communications for that product.
  • Provide suitable summaries of product risks to summary document authors where appropriate
  • Perform ad hoc special activities, rapidly, to meet specific needs in the BUs, such as deliverables/emerging safety issue white papers/product Due Diligence Assessments
  • Identify opportunities for Consistency and Standards for Safety Surveillance (SS) and Risk Management (RM) approaches and processes within and across BUs, and supporting the piloting and implementation of such
  • Innovating, championing and implementing Novel Approaches across BUs:
  • Engagement in Continuous Improvement initiatives, Safety Sciences Research & Communications activities, including methodological improvements
  • -Engagement in inspection readiness and support.
  • Provision of data to project managers for metrics and activity tracking

 

To be considered for this Drug Safety Lead position, you will have the following qualifications, skills and experience:

– MD, PhD, PharmD, DVM, MSc, or equivalents, and appropriate Pharma experience in SS & RM.

– Thorough understanding of Safety Risk Management internal and external environment, including applicable regulations and guidances.

– Displays a sound understanding of the scientific basis for therapies and drug-induced diseases. Comprehensive knowledge of drug development process.

– Clinical development and post-marketing experience to have an understanding of safetycontext across the drug lifecycle.

– Able to act independently, seeking guidance as appropriate. Demonstrates leadership in day-to- day activities and collaborative skills.

– Can handle more than one complex project simultaneously, prioritizing welland recognizing key issues.

– Ability in, and track record of, working effectively in an advanced matrix structure, including matrix team leadership/representation preferred.

– Recognizes other colleagues’ areas of expertise and utilizes them effectively to achieve team objectives. Runs effective meetings, including all colleagues’ diverse opinions and bringing group to consensus. Next steps and actions are clear.

– Effective verbal and written communication skills in relating to colleagues and associates both inside and outside the organization.

– Relevant knowledge of Pharmaceutical Company organizational structure, policies, and practices, as applicable to safety Risk Management.

 

How to apply

Click here to apply online, or contact Hendre Moolman on 01438 870 023 or email hmoolman@ckclinical.co.uk. Please quote reference CL23369  in all correspondence.

Search our current drug safety jobs now.

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Biostatistician Job – South East, UK

A Biostatistician is required to work closely with scientists seeking to discover new medicines to treat diseases in the Respiratory/Inflammation and Oncology therapy areas.

You will be involved in the design and analysis of discovery and pre-clinical experiments, disease area investigations, bio analytical assay development, biomarker development and other aspects of drug discovery from disease target identification, model development to the demonstration of proof of concept in treatment. The responsibilities of this position can evolve over time to include support of early clinical trial work in these (and other) disease areas.

Interested applicants for this Biostatistician position should be MSc qualified (or hold the equivalence) in Statistics or Biostatistics with proven experience with the Pharmaceutical/CRO/Biotechnology environment. Alternatively, applications are welcome from those holding a PhD in Statistics/Biostatistics who are looking to enter the Pharmaceutical arena. Preferred candidates will also have statistical skills in R (and S-plus or SAS environments).

 

Apply Now

For more information or to apply for this Biostatistician position, please contact Priya Mukherjee at CK Clinical on 01438 743 047 or email pmukherjee@ckclinical.co.uk.

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

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Regional Scientific Liaison Manager Job – Buckinghamshire, UK

We are recruiting for Regional Scientific Liaison Manager to join a Pharmaceutical company in Buckinghamshire in a field-based position.

As Regional Scientific Liaison Manager you will initiate and maintain strong relationships with opinion leaders. You will also provide medical input at a regional level to enable business opportunities to be maximised and new leads created and developed within current regulatory and code requirements.

Further key responsibilities of this Regional Scientific Liaison Manager role ill include:

  • Responsibility for medical input at a regional level to enable business opportunities to be maximised and new leads created and developed within current regulatory and code requirements.
  • Contribution to the development and implementation of the medical – marketing strategy for key brands.
  • Development and fostering of relationships with key clinical and non-clinical customers as required by the regional plan.
  • Contribution to the identification and evaluation of Business Development opportunities at a local, national, cluster and corporate level.
  • Responsibility for the provision of medical input to relevant national, regional and local Market Access submissions.
  • Responsibility for the ongoing management of relevant Investigator Initiated Trials and some company clinical trials in conjunction with internal clinical resource.
  • Responsibility for the medical sign off of relevant promotional and non-promotional material in line with the company SOPs and ABPI Code of Practice.
  • Develop and foster excellent relationships with KOLs in the relevant therapeutic areas and maintain regular contact with them in conjunction with other functions.

The ideal candidate for this Regional Scientific Liaison Manager position will have the following knowledge and experience:

  • Life science degree, ideally to PhD level but nursing/healthcare/pharmacist qualification will be considered.
  • At least 18 months experience within medical department of a pharmaceutical company.
  • Knowledge and understanding of the clinical trials process desirable – especially Phase III, IV and IITs.
  • Thorough knowledge of the ABPI Code of Practice, Medicines Act and MHRA Blue Book is essential – both in the field as well as implementation in approval processes for materials.
  • An understanding of Market Access processes e.g. SMC, AWMSG, and formulary applications preferable.
  • An understanding/exposure to/experience in Business Development would be an advantage.

The successful candidate for this Regional Scientific Liaison Manager position will enjoy the benefits of working with a global Pharmaceutical company, including a COMPETITIVE SALARY, HOLIDAYS, and CAREER PROGRESSION.

Apply Now

For more information or to apply for this Medical Liaison Manager please contact Hendre on Tel: +44 (0)1438 743047 or email me at hmoolman@ckclinical.co.uk quoting 20000 to indicate your interest.

Alternatively, click here to apply for this Regional Scientific Liaison Manager position online now.

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Director/Senior Director (Internal Medicines) – Hertfordshire, UK

  • Salary £95-105K (negotiable)
  • Car allowance
  • Bonus
  • Good benefits

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.

 

Apply Now

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.

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Regional Scientific Liaison Manager – Field Based

Regional Scientific Liaison Manager / Scientific Advisor / Medical Liaison

We are recruiting for Regional Scientific Liaison Manager to join a Pharmaceutical company in Buckinghamshire in a field-based position. This is a permanent position. 

As Regional Scientific Liaison Manager, you will initiate and maintain strong relationships with opinion leaders. You will provide medical input at a regional level to enable business opportunities to be maximised and new leads created and developed within current regulatory and code requirements. Previous experience in working in a similar position is preferred, with knowledge and understanding of the clinical trials process desirable. The territory that will be covered in this position is dependant on where in England you are based.

Key responsibilities:
-Responsibility for medical input at a regional level to enable business opportunities to be maximised and new leads created and developed within current regulatory and code requirements.
– Contribution to the development and implementation of the medical – marketing strategy for key brands.
– Development and fostering of relationships with key clinical and non clinical customers as required by the regional plan.
– Contribution to the identification and evaluation of Business Development opportunities at a local, national, cluster and corporate level.
– Responsibility for the provision of medical input to relevant national, regional and local Market Access submissions.
– Responsibility for the ongoing management of relevant Investigator Initiated Trials and some company clinical trials in conjunction with internal clinical resource.
– Responsibility for the medical sign off of relevant promotional and non- promotional material in line with the company SOPs and ABPI Code of Practice.
– Develop and foster excellent relationships with KOLs in the relevant therapeutic areas and maintain regular contact with them in conjunction with other functions.

Knowledge and experience
– Life science degree, ideally to PhD level but nursing/healthcare/pharmacist qualification will be considered.
– At least 18 months experience within medical department of a pharmaceutical company.
– Knowledge and understanding of the clinical trials process desirable – especially Phase III, IV and IITs.
– Thorough knowledge of the ABPI Code of Practice, Medicines Act and MHRA Blue Book is essential – both in the field as well as implementation in approval processes for materials.
– An understanding of Market Access processes e.g. SMC, AWMSG, and formulary applications preferable.
– An understanding/exposure to/experience in Business Development would be an advantage.

Benefits
Successful candidates will enjoy the benefits of working with a global Pharmaceutical company, including a COMPETITIVE SALARY, HOLIDAYS, and CAREER PROGRESSION.

About CK Clinical
Finding a new job can be a rather daunting process. At CK Clinical we pride ourselves in our honest and supportive approach. This is the reason why nearly 50% of people we help are referred to us by their colleagues and friends. CK Clinical are preferred suppliers to the top 5 global organisations within our sector as well as having agreements in place with smaller, more niche organisations too.

Apply now

If you expect more than just a great salary and benefits package and believe you can make an impact in this innovative and cutting edge business, then please contact Hendre on Tel: +44 (0)1438 743047 or email me at
hmoolman@ckclinical.co.uk quoting 20000 to indicate your interest.

Alternatively, click here to apply for this Regional Scientific Liaison Manager role online now.

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Medical Liaison Required for Established Pharmaceutical Company based in Hampshire, UK

A new opportunity has arisen to join an established pharmaceutical company in Hampshire as a Medical Liaison. You will support key business needs across therapeutic areas based upon the needs of the clinical experts.

The focus of this Medical Liaison role will be to provide a non-promotional scientific information service for external customers, supporting and enhancing the safe and effective use of products, enabling customers to make informed decisions. GMC registration is not required.

The key responsibilities of this Medical Liaison role will include:

  • Catch therapy trends and/or other developments in the specific therapeutic area
  • Share feedback of external experts internally (Voice of the customer), e.g. expert’s impression of clinical data, experts view of general therapeutic area landscape, experts reaction to promotional pieces, experts research interests
  • Share learning from publications, external meetings and other adequate channels internally
  • Play a role in management of product issues
  • Provide recommendations about potential new investigators to Clinical Operations
  • Identifying future national and regional experts
  • Identifying national, sub-national/local influence or advocacy groups for their assigned product(s)
  • Serve as an educational source for Sales Reps, including actively participating in the training of Sales Reps
  • Provide input on development of brand strategies based on knowledge of the specific therapeutic area

The successful candidate for this Medical Liaison job will ideally have a Health or Life Sciences related degree at postgraduate qualification level. You will also have relevant experience of working in a health science or related environment (e.g. clinical research/CRO, pharmacy, nursing or R&D). The following competencies are also desirable:

  • Demonstrated ability to develop working relationships with thought leaders either in a research or pharmaceutical industry setting
  • Demonstrated project implementation and management skills
  • Good presentation, written & verbal skills

How to apply:

For more information, or to apply for this Medical Liaison role, please contact Hendre on Tel: +44 (0)1438 870 023 or email at hmoolman@ckclinical.co.uk quoting 19456 to indicate your interest.

Alternatively, click here to apply for this Medical Liaison job now.

 

About CK Clinical

Here at CK Clinical, we pride ourselves on our honest and supportive approach. Our team of specialist recruiters and career consultants are here to help you achieve your career ambitions within the clinical and pharmaceutical industry. We can actively offer you careers advice, help with writing your CV, assistance with your interview preparation and provide you with up to date information about the industry.

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