Medial Research Network

Careers

MRN is constantly looking for experienced team members, keen to explore new projects and motivated to embrace new ideas and challenges, in both our UK and US offices. If you are interested in any of these roles listed below or keen to explore future opportunities please send your CV and a brief covering letter to Kellie Bryant in the first instance;

Study Training Associate (Maternity Cover) - Milton Keynes - UK

As a Study Training Associate, you will have full responsibility for the coordination, on-boarding and training of clinical home trial support professionals.

To be considered for the role, you must be able to demonstrate:

  • Previous experience of working in a busy office environment
  • Confident and engaging communication skills both written and verbal
  • The ability to manage relationships with internal and external stakeholders
  • Proficiency in Microsoft Office applications
  • Knowledge of data entry and tracking
  • The ability to work independently and organise and prioritise workloads effectively

Key responsibilities include:

  • Tracking nurse training progress to ensure nurses are trained and signed off in a timely manner
  • Liaising with the vendor country leads for identification of suitable healthcare professionals
  • Arranging access to training portal and training modules
  • Monitoring test attempts
  • Marking manually administered test papers
  • Following up with HcP on any outstanding training and training documentation
  • Provide daily updates to the project teams on nurse training progress
  • Producing weekly reports on training metrics
  • Producing daily reports on HcP documents due for a visit assessment quality check
  • Formatting new documents in Powerpoint, Word and Excel as required
  • Weekly Nursing division meeting scheduling and minute taking.

Why join us?

  • A competitive basic salary
  • Generous pension and holiday schemes
  • Wider benefits including life insurance, health insurance and Perkbox
  • An inclusive and collaborative working culture
  • Fantastic opportunities for future growth and career progression

If you feel you have the relevant skills and experience to be a success, please Apply Today!

Data Protection – Your Rights

Should you apply for a job opportunity at The MRN, we wish to inform you that it is our intention to retain the personal data provided by you for up to 2 years from the date it is received, at which point you will be asked to provide new consent. If you have any questions or concerns regarding our processes and how your personal data will be stored, please contact us for further reassurance.

 

Project Support Associate - Clinical Trials - Skokie, IL

Project Support Associate (Clinical Trials) – Skokie, IL

A full-time, permanent position offering a competitive salary and fantastic opportunities for career progression!

Due to extensive growth, we are looking to expand our Project Management team in Skokie, IL. As a Project Support Associate, you will facilitate the management and delivery of Clinical Trial Support studies and provide administrative support within the Operations division.

If you have a science-related degree and previous experience of working in an office and/or clinical /pharma environment, then we would love to hear from you!

Who we are looking for:

An individual with...

  • Good IT skills - Intermediate understanding of and ability to use MS Office
  • Previous experience of working in an administrative or project-based role
  • Knowledge of the principles of ICH-GCP
  • Strong communication skills, both written and verbal
  • The ability to work on own initiative and without daily supervision
  • Enthusiasm and a desire to work as part of a friendly and committed team

 

Key Responsibilities and Duties:

Study set up

  • Using corporate templates as starting point design key study documents e.g.- Drug transportation and shipment forms, site to homecare handover forms, liaising with customer/sponsor to revise and finalise documents according to agreed study timelines.
  • Sending of nurse documents, CVs, training logs, signed delegation logs to site prior to first home visit.

Ongoing study

  • Acknowledging receipt of referrals, reviewing of information and liaising with site staff to ensure original all documentation is received in a timely manner

Study completion

  • Assisting with the return of study equipment and other close out activities

Why join us?

  • Competitive base salary
  • Annual bonus program
  • 401(k) plan with company match
  • Generous paid time off allowance
  • Paid company holidays
  • Health, dental, vision and life insurance plans
  • Fantastic opportunities for future career development
  • An inclusive and collaborative working culture

If you feel you have the relevant skills and experience to be a success, please Apply Today!

Data Protection – Your Rights

Should you apply for a job opportunity at The MRN, we wish to inform you that it is our intention to retain the personal data provided by you for up to 2 years from the date it is received, at which point you will be asked to provide new consent. If you have any questions or concerns regarding our processes and how your personal data will be stored, please contact us for further reassurance.

 

Paediatric Nurse - Home Trial Support - UK wide

 

Are you looking for interesting and flexible work to boost your monthly salary?

Location: Nationwide with immediate opportunities in the North East, Midlands and South London

Hours: Variety of flexible working patterns available

The Medical Research Network is the leader in the innovative field of providing clinical trial treatment in a patient’s home. We work with nurses around the UK to administer study drug, collect safety bloods and conduct other clinical activities.

This is an excellent opportunity for experienced, highly motivated nurses to join a unique organisation and positively impact patients’ quality of life. Additionally, you will be working on ground-breaking trials, which can provide new and improved treatments.

We are currently recruiting registered Paediatric Nurses with at least two years’ experience who can demonstrate the following:

  • Experience as a Research Nurse is highly desirable
  • Experience in administration of intravenous therapies (Mandatory)
  • Cannulation and phlebotomy skills are essential
  • Experience in using Central Venous access Devices (Mandatory)
  • Knowledge of providing nursing in the community/home environment would be an advantage
  • Enthusiastic, positive attitude with great attention to detail.
  • Great organisational skills and ability to plan visit activities independently.
  • Excellent communication skills and the ability to complete complex data requirements.
  • Please note, you will be required to travel so a full driving licence and access to a vehicle is a must!

In return we can offer you:

  • Excellent rates of pay
  • Flexible working hours/shift patterns
  • Travel allowance/expenses
  • Training and continuing education (including ICH-GCP training if required)
  • Unique and varied clinical experiences

If you feel you have the skills, experience and attitude then please Apply Today for immediate consideration!

Data Protection – Your Rights

Should you apply for a job opportunity at The MRN, we wish to inform you that it is our intention to retain the personal data provided by you for up to 2 years from the date it is received, at which point you will be asked to provide new consent. If you have any questions or concerns regarding our processes and how your personal data will be stored, please contact us for further reassurance

Home Trials Research Nurses - USA , Various Locations including Seattle, Chicago and New York

Are you looking for a flexible opportunity to enhance your monthly income?

The Medical Research Network is the leader in the innovative field of providing clinical trial treatment in a patient’s home. We work with nurses around globe to administer study drugs, collect safety bloods and conduct other clinical activities.

This is an excellent opportunity for experienced, highly motivated nurses to join a unique organisation and positively impact patients’ quality of life. Additionally, you will be working on ground-breaking trials, which can provide new and improved treatments.

We are currently recruiting registered Paediatric and Adult Nurses with at least two years’ experience who can demonstrate the following:

  • Experience as a Research Nurse is highly desirable
  • Experience in administration of intravenous therapies (Mandatory)
  • Cannulation and phlebotomy skills (Mandatory)
  • Experience in using Central Venous access Devices (Mandatory)
  • Knowledge of providing nursing in the community/home environment would be an advantage
  • Enthusiastic, positive attitude with great attention to detail.
  • Great organisational skills and ability to plan visit activities independently.
  • Excellent communication skills and the ability to complete complex data requirements.
  • Please note, you will be required to travel so a driving licence and access to a vehicle is essential!

In return we can offer you:

  • Excellent rates of pay
  • Flexible working hours/shift patterns
  • Travel allowance/expenses
  • Training and continuing education (including ICH-GCP training if required)
  • Unique and varied clinical experiences

If you feel you have the skills, experience and attitude to be a success, then please Apply Today for immediate consideration!

Data Protection – Your Rights

Should you apply for a job opportunity at The MRN, we wish to inform you that it is our intention to retain the personal data provided by you for up to 2 years from the date it is received, at which point you will be asked to provide new consent. If you have any questions or concerns regarding our processes and how your personal data will be stored, please contact us for further reassurance

Job Types: Part-time, Temporary, Contract

Compliance Coordinator - Milton Keynes - UK

 

Due to our continued success we are looking to recruit an experienced Compliance Coordinator to join our talented Quality Management team in Milton Keynes.

As a Compliance Coordinator, you will support the development and maintenance of Controlled Documents as part of our Quality Management System. You will support the planning, preparation and conduct of MRN’s independent audit program, including internal & external audits and inspections in alignment with our Quality Management Procedures.

To be considered for this role, you must be able to demonstrate the following:

  • A Bachelor of Science BSc (Hons) 2.2 or above (or equivalent) degree
  • Experience of proof-reading and managing Controlled Documents or similar, within the clinical trials or pharmaceutical industry
  • A detail orientated approach, with a view to providing first-time, high-quality output
  • Knowledge of the clinical trials regulations, auditing and inspection process
  • Confident and engaging communication skills both written and verbal
  • The ability to manage relationships with internal and external stakeholders
  • The ability to work independently and proactively
  • Proficiency in Microsoft Office applications

Why join us?

  • A competitive basic salary
  • Generous pension and holiday schemes
  • Wider benefits including life insurance, health insurance and Perkbox
  • An inclusive and collaborative working culture
  • Fantastic opportunities for future growth and career progression

As a Compliance Coordinator, your primary responsibilities will include:

  • Providing support to the wider business for the creation, maintenance and storage of controlled documents.
  • Ensuring controlled documents are within the review cycles set-forth by the Quality Management procedures.
  • Responsibility for the updating and release of controlled documents and SOPs.
  • Overseeing the day to day running and maintenance of the controlled document access and management process.
  • Be the point person for any questions or issues within MRN on controlled documents.
  • Generating KPIs regarding controlled documents and reports on the status of existing and draft controlled documents.
  • Liaising with the Training team to ensure controlled documents are released and made available in the internal LMS as required.
  • Supporting and coordinating audits, project reviews and inspections.
  • Managing and updating all QM Controlled Document trackers.

If you feel you have the relevant skills and experience to be a success, please Apply Today!

Data Protection – Your Rights

Should you apply for a job opportunity at The MRN, we wish to inform you that it is our intention to retain the personal data provided by you for up to 2 years from the date it is received, at which point you will be asked to provide new consent. If you have any questions or concerns regarding our processes and how your personal data will be stored, please contact us for further reassurance.

Project Manager - Milton Keynes

Project Manager – Milton Keynes

As part of our continued growth, The Medical Research Network is currently looking to recruit a full time, permanent, Project Manager to join our talented team in Milton Keynes.

As a Project Manager with the MRN you will successfully deliver complex home trial projects on time and within budget, and in accordance with international laws and guidelines.

Who are we looking for?

  • You must have strong experience to include sponsor/CRO, and or site clinical research exposure
  • Proven effectiveness in leading a cross functional teams
  • Proven experience in planning and delivering projects on time and to budget
  • Working knowledge of ICH GCP and appropriate regulatory laws and guidelines
  • Understanding of project financial management and be able to demonstrate commercial awareness
  • Ability to multi-task, problem solve and prioritise complex workload
  • Able to work with and present top line overview and in-depth detail of projects

Responsibilities will include;

  • Organising and leading internal project meetings to ensure projects run smoothly and any issues are raised, discussed and resolved effectively.
  • Attending and reporting progress to external project teams and clients, discussing customer plans and tracking information to ensure projects remain on track.
  • Reporting to VP Nursing & Operations ensuring plans are fully updated and accurate reports created.
  • Regular interaction with other internal groups for the provision of cost information, status of supplier contracts etc.

 

  • Why join us?
    • A competitive basic salary
    • Generous pension and holiday schemes
    • Wider benefits including life insurance, health insurance and Perkbox
    • An inclusive and collaborative working culture
    • Fantastic opportunities for future growth and career progression

If you feel you have the relevant skills and experience to be a success, please Apply Today!

Data Protection – Your Rights

Should you apply for a job opportunity at The MRN, we wish to inform you that it is our intention to retain the personal data provided by you for up to 2 years from the date it is received, at which point you will be asked to provide new consent. If you have any questions or concerns regarding our processes and how your personal data will be stored, please contact us for further reassurance.

Project Support Associate - Clinical Trials - Milton Keynes - UK

Project Support Associate (Clinical Trials) – Milton Keynes

A full-time, permanent position offering a competitive salary and fantastic opportunities for career progression!

Due to extensive growth, we are looking to expand our Project Management team in Milton Keynes. As a Project Support Associate, you will facilitate the management and delivery of Clinical Trial Support studies and provide administrative support within the Operations division.

If you have a science-related degree and previous experience of working in an office and/or clinical /pharma environment, then we would love to hear from you!

Who we are looking for:

An individual with...

  • Good IT skills - Intermediate understanding of and ability to use MS Office
  • Previous experience of working in an administrative or project-based role
  • Knowledge of the principles of ICH GCP
  • Strong communication skills, both written and verbal
  • The ability to work on own initiative and without daily supervision
  • Enthusiasm and a desire to work as part of a friendly and committed team

Key Responsibilities and Duties:

Study set up

  • Using corporate templates as starting point design key study documents e.g.- Drug transportation and shipment forms, site to homecare handover forms, liaising with customer/sponsor to revise and finalise documents according to agreed study timelines.
  • Sending of nurse documents, CVs, training logs, signed delegation logs to site prior to first home visit.

Ongoing study

  • Acknowledging receipt of referrals, reviewing of information and liaising with site staff to ensure original all documentation is received in a timely manner

Study completion

  • Assisting with the return of study equipment and other close out activities

 

Why join us?

  • A competitive basic salary
  • Generous pension and holiday schemes
  • Wider benefits including life insurance, health insurance and Perkbox
  • An inclusive and collaborative working culture
  • Fantastic opportunities for future growth and career progression

If you feel you have the relevant skills and experience to be a success, please Apply Today!

Data Protection – Your Rights

Should you apply for a job opportunity at The MRN, we wish to inform you that it is our intention to retain the personal data provided by you for up to 2 years from the date it is received, at which point you will be asked to provide new consent. If you have any questions or concerns regarding our processes and how your personal data will be stored, please contact us for further reassurance.

 

Project Manager - Skokie, IL

Project Manager – Skokie, IL

As part of our continued growth, The Medical Research Network is currently looking to recruit a full time, permanent, Project Manager to join our talented team in Skokie.

As a Project Manager with the MRN you will successfully deliver complex home trial projects on time and within budget, and in accordance with international laws and guidelines.

Who are we looking for?

  • You must have strong experience to include sponsor/CRO, and or site clinical research exposure
  • Proven effectiveness in leading a cross functional teams
  • Proven experience in planning and delivering projects on time and to budget
  • Working knowledge of ICH GCP and appropriate regulatory laws and guidelines
  • Understanding of project financial management and be able to demonstrate commercial awareness
  • Ability to multi-task, problem solve and prioritise complex workload
  • Able to work with and present top line overview and in-depth detail of projects

Responsibilities will include;

  • Organising and leading internal project meetings to ensure projects run smoothly and any issues are raised, discussed and resolved effectively.
  • Attending and reporting progress to external project teams and clients, discussing customer plans and tracking information to ensure projects remain on track.
  • Reporting to VP Nursing & Operations ensuring plans are fully updated and accurate reports created.
  • Regular interaction with other internal groups for the provision of cost information, status of supplier contracts etc.

What we can offer you:

  • Competitive base salary
  • Annual bonus program
  • 401(k) plan with company match
  • Generous paid time off allowance
  • Paid company holidays
  • Health, dental, vision and life insurance plans
  • Fantastic opportunities for future career development

If you feel you have the relevant skills and experience to be a success, please Apply Today!

Data Protection – Your Rights

Should you apply for a job opportunity at The MRN, we wish to inform you that it is our intention to retain the personal data provided by you for up to 2 years from the date it is received, at which point you will be asked to provide new consent. If you have any questions or concerns regarding our processes and how your personal data will be stored, please contact us for further reassurance.

 

Non-Clinical Country Lead US - Skokie IL

Non-Clinical Country Lead (Clinical Trials) – Skokie, IL

The Medical Research Network (MRN) specialise in providing home-based clinical trials to patients across the globe and are looking to recruit a Non-Clinical Country Lead to join our talented and friendly team in Skokie, IL.

As an NCCL, you will schedule and manage visits conducted by MRN's Internal Nurse Network in the US and work closely with internal project management teams to facilitate execution of Home Trial Support (HTS) Studies. This is a faced paced role that focusses on daily deliverables and MRN are looking for someone who can think strategically but also has strong attention to detail to provide a quality service to our clients.

To be considered for this role, you must be able to demonstrate the following:

  • Previous experience of working within a busy office environment, ideally within the healthcare/nursing arena.
  • This is a busy and varied role so you must be highly organised and able to manage workload and priorities effectively
  • A proficient user of Microsoft Office Suite (Word, Excel and PowerPoint) and Adobe Acrobat.
  • High attention to detail is critical
  • A calm, methodical and solution focused approach
  • Excellent communication skills, both verbal and written
  • Process oriented but with the ability to be flexible when required
  • Analytical and able to use initiative and strong decision-making skills
  • Desire and ability to develop new skills

What we can offer you:

  • Competitive base salary
  • Annual bonus program
  • 401(k) plan with company match
  • Generous paid time off allowance
  • Paid company holidays
  • Health, dental, vision and life insurance plans
  • Fantastic opportunities for future career development

If you feel you have the relevant skills and experience to be a success, please Apply Today!

Data Protection – Your Rights

Should you apply for a job opportunity at The MRN, we wish to inform you that it is our intention to retain the personal data provided by you for up to 2 years from the date it is received, at which point you will be asked to provide new consent. If you have any questions or concerns regarding our processes and how your personal data will be stored, please contact us for further reassurance.

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