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RBW are recruitment specialists with the Pharmaceutical, MedTech, Healthcare Communications, IT & HR industries. Working on a global basis, we have been exceeding expectations since 2007.

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Medical Science Liaison, Cardiovascular

Ref: RNBW-MSL-12018

Location: South West Territory, UK

Type: Permanent


A Global pharmaceutical company

A permanent position as an MSL in Cardiovascular for a Global pharmaceutical company, offering a comprehensive reward and benefits package. Opportunity to be involved in a time of growth for the company and a new product launch.


Summary
An MSL is required to join a well-established and expanding pharmaceutical company based in the South of the UK. In this role, you will be tasked with providing expert support to external customers and healthcare professionals.


Key Responsibilities
As Medical Science Liaison, you will be required to fulfil the following duties:

  • Acting as point of contact for sales professionals to gain answers to medical questions which would require expert knowledge.
  • Developing and maintaining contacts with thought leaders to gain insight into treatment patterns, scientific activities and the needs of healthcare providers ongoing in the disease area.
  • Developing and contributing to scientific presentations.
  • Providing input to the clinical trials team on trial and survey feasibility.
  • Performing all the above in an ethical and legally compliant manner, in accordance with company SOPs and the ABPI code of practice.


Requirements
Should you wish to apply for this position, please ensure meet the following requirements:

  • Industry experience as a Medical Science Liaison.
  • Degree in either medicine, nursing, pharmacy or life sciences.
  • Full UK drivers licence and ability to travel within the region.
  • Proven experience of presenting scientific information to healthcare professionals.
  • Knowledge of the UK National Healthcare System.

 

Salary: On application

 

Full details

Clinical Research Physician - Entry Level

Ref: RNBW-CRP/NWUK-12078

Location: North West, UK

Type: Permanent


A great opportunity for someone currently in the NHS or private practice looking to get into industry

A great opportunity for someone currently in the NHS or private practice looking to get into industry, huge development opportunities with an impressive salary and benefits package as well.
An excellent chance for a physician or GP with a keen interest in the clinical trials or the pharmaceutical industry to play an instrumental role in driving this organisation towards success.

 

Responsibilities
As a Research Physician, you will be responsible for ensuring the commercial success of your site through the safe performance of your local clinical studies. You will also be supported to build upon your experience and expertise to enable you to act as Co-Investigator where you will accept responsibility for all sponsor research studies while ensuring ICH/GCP and local regulations are met.

 

Your key accountabilities will include;

  • Acting as Co-Investigator ensuring ICH/GCP and local regulations are met
  • Conducting clinical trials in line with the protocol and to ensure the recruitment of eligible participants onto study
  • Taking ownership of being prepared for all GMC appraisals to ensure we see a positive outcome
  • Reviewing screening, pre-screening and screening success rates for clinical trials
  • Providing information and support to consenting participants for a clinical study
  • Liaising with and developing positive relations with sponsors, clients and clients’ contractors as required, projecting a helpful and courteous company image
  • Carrying out clinical evaluation and clinical investigation of participants
  • Constantly seeking and suggesting quality improvements
  • Taking responsibility for ensuring serious adverse events / adverse events are reported appropriately
  • Having responsibility for the medical wellbeing of participants during the clinical trial and referral to specialists or GP as required

 

Requirements
In order to be considered, please ensure you meet the following criteria:

  • GMC registered doctor with a good level of post graduate clinical experience
  • Have little or no previous research experience, however, you should demonstrate a strong interest in clinical research
  • Have working knowledge of GCP (ICH-GCP and local regulations compliance)
  • Demonstrate the ability to follow study protocol’s and standard operating procedures (SOP’s) at all times
  • Exercise meticulous attention to detail in recording patient information and data

 

Salary: On application

 

Full details

Back End Developer

Ref: VR/07223

Location: East Sussex, UK

Type: Contract


3 month rolling contract – Must have Winforms experience – For a field leading organisation

Job Summary

We are seeking an experienced C# Developer, with experience of AgileScrum development, to join an existing team delivering bespoke software solutions in a C# .NetSQL Server environment

 

Essential Job Duties

  • Coding of new application functionality using C# / SQL server 
  • Maintenance & modification of existing applications, services and websites.
  • Resolution of escalated developer oriented helpdesk issues

 

Education and Experience Requirements

You will have an extensive development background with extensive experience in a similar role and proven track record of building quality corporate applications and delivering them on time.

 

Essential skills

  • Strong C#
  • Web API
  • JavaScript frameworks (ideally Angular 2)
  • Entity Framework
  • ASP.net
  • WCF Services 
  • Windows Forms 
  • MVC  
  • SQL Server
  • Build / deployment platforms (TeamCity / Octopus)

 

Desirable skills

  • Messaging Queuing technologies
  • TDD
  • Lo-CodeNo-Code BPM Platforms (e.g. Appian)

 

Salary: £350 - £375 per day 

 

Full details

Associate Director Regulatory Affairs

Ref: AC/ADRA/BEL

Location: Belgium, Europe

Type: Permanent


One of the most exciting Biotech groups

One of the most exciting Biotech groups with key offices in the US and EU are now currently looking to appoint a highly skilled “Associate Regulatory Affairs Director’ to spearhead a number of exciting and challenging projects on a global basis.

 

In this exciting role, the successful applicant will be a key driver responsible for the Regulatory Affairs Strategy globally predominately for development projects. In addition, the role offers tremendous autonomy; a chance to help others grow and to participate in a group with huge potential on an international basis.

 

Responsibilities:

  • Leadership and development of the RA Strategy on a global basis for development projects
  • Set a strategy with the overall goal of product registration in all global markets.
  • Build strong relationships and advocacy with the regulatory agencies – both at the local, nationally – as well as with notified bodies and international regulatory authorities (FDA & EMA)
  • Manager Scientific meetings and follow up with key global competent authorities 
  • Can understand possible areas of Risk and act accordingly on a strategic and operational basis
  • Provide direct support to team colleagues through direct and indirect management
  • Communicate Regulatory plans and progress with all necessary internal and external stakeholders
  • Collaborate with fellow Regulatory colleagues on other aspects in the Regulatory cycle to achieve the common overall goal (CMC team members)
  • Work with other key areas of the business to support strategic development from a Regulatory perspective
  • Ensure all documentation for successful submissions is completed to the required level
  • Participate in the group and support the Executive leader of Regulatory Affairs when required  

 

Skills needed:

  • Master’s degree in Life sciences area or related field
  • Demonstrated experience working in Regulatory Affairs with Biological products
  • Experience working with ATMP products would be preferred but not essential
  • Have a distinct background in Regulatory strategy design for development products
  • Must have a demonstrated background dealing with Competent authorities
  • Ideally skilled in managing others 
  • Driven, passionate and motivated
  • Excellent communication skills
  • Can work office based in Belgium

 

If you feel you match the  qualities we are looking for  and the role appeals to you , please contact Antony Clark at RBW Consulting on +44 1293 584300. Alternatively, please email me at antony.clark@rbwconsulting.com for full details.

 

At RBW Consulting Ltd, every one of our consultants has the benefit of multiple years’ experience in helping Pharmaceutical & Medical Device Professionals find the right career step for their current and future aspirations. With unrivalled industry knowledge and network in Biotech’s, Pharmaceutical and Medical Device Companies throughout the UK, Switzerland and Europe, we would be delighted to speak with you about the role you are looking for.

 

Salary: 80,000 - 90,000 Per annum

 
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When only the best will do

RBW Consulting was formed in 2007 with a vision to create a consultancy offering a thoroughly modern approach to recruitment that would stand out from the rest. Drawing upon combined recruitment experience of over 30 years, Nick, Andrew and Richard set out to build a company that provides a genuine, intelligent service to our clients.

We are very proud of the reputation we have built and have worked successfully with companies on a global basis, from the very largest to the smallest, and we have rapidly gained a reputation for yielding the best results, quickly.

Fundamental to these successes are the relationships we have developed with our candidates and clients: we aim to operate completely transparently, maintaining regular contact and encouraging two-way dialogue throughout. We understand that long term relationships are fundamental to our continued growth

Work For Us

Are you a Recruiter or sales person looking for a new career opportunity? If so, we would love to hear from you! 

Central to RBW Consulting's continued success has been the standard of our top-level consultants. As we look to expand and grow even further we are always interested in finding individuals to join our team.

Contact Michelle Jones for a confidential conversation about what life would look like here!

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The RBW Development Academy

RBW has a fantastic in-house training department who provide training and support for all of the RBW Consulting team. 

The department is headed up by Michelle Jones who is also responsible for running the RBW Development Academy. This is our in house training programme which covers all aspects of the recruitment life cycle. Our training results in faster promotion and development, as well as offering the foundations to build a rewarding and lucrative career.

Click here to apply to join the Academy!