Clinical Trial Manager

myGwork - LGBTQ+ Business Community; United Kingdom; Remote; GBP 50,000 - 75,000; Full time

Benefits offered by this job

Solid structured on-boarding

Comprehensive total reward package

Best-in-class employee benefits

Job summary

A leading biotechnology company is seeking a Clinical Trial Manager to collaborate on global clinical trial strategy, requiring solid experience in biopharmaceuticals and clinical research. This role offers the flexibility of being fully home-based in the UK and includes a permanent contract with opportunities for professional development.

Qualifications

• 5 years’ work experience in life sciences, including 2 years in clinical trials.
• Experience with vendor interactions and project planning.
• Solid organization and planning skills required.

Responsibilities

• Support clinical trial strategy execution and monitor trial deliverables.
• Contribute to preparation of study-related documents.
• Coordinate activities for trial management and site start-up.

Skills

Risk assessment

Project Management

Vendor management

Critical thinking

Communication

Education

BS/BA/BSc in the sciences or RN

Job description

Join to apply for the Clinical Trial Manager role at myGwork - LGBTQ+ Business Community

1 day ago Be among the first 25 applicants

Join to apply for the Clinical Trial Manager role at myGwork - LGBTQ+ Business Community

This job is with ICON plc, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly.

We are hiring a Clinical Trial Manager to start asap!

The role can be fully homebased in the UK and this is anon-travelling position.

This is a great opportunity to steer your career towards clinical trial management. It would suit a Junior CTM,or experienced Senior Clinical Project Specialist with solid multiple country exposure, looking for their first CTM position. Global clinical trial experience is essential to succeed!

You will be part of an innovative and global Biotechnology company, who pride themselves to be one of the world's leading independent biotechnology companies. They focus on areas with unmet medical need with the ambition to help reduce the social and economic burden of disease in society today.

The role

• Support the Global Clinical Trial Manager, Global Early Clinical Development Manager, Local Trial Manager, Regional or Country Study Manager in the delivery of the clinical and operational strategy and assist the execution of clinical trials
• Vendor management and support vendor relationships
• Work with the clinical trial management staff to support the execution and monitoring of clinical studies and trial deliverables
• Contribute to and support with the preparation, writing and review of study related documents including but not limited to, clinical protocols, study guides, monitoring plans, e(CRF)s, subject information sheets and consent forms, clinical study report, regulatory submissions and publications
• Coordinate the activities associated with site start-up and overall trial management
• Coordinate study level investigational product arrangements, accountability and reconciliation
• Contribute to, or coordinate preparation and conduct of site initiations, monitors’ workshops (as applicable) and investigator meetings (as applicable)
• Assists in preparing and managing Study Budgets and timelines
• Coordinate study level investigational product arrangements and study start-up and management activities
• Performprotocol-related site management activities
  
  

What Is Required

• BS/BA/BSc in the sciences preferred or RN or above
• 5 years’ work experience, ideally, in life sciences or medically related field, including 2 years of direct biopharmaceutical clinical research experience obtained working on clinical trials at a biotech, pharmaceutical or CRO company
• Project Management, project planning experience including oversight of study deliverables, budgets, and timelines
• Experience interacting with external vendors (CROs, central labs, imaging vendors, etc.)
• Experience with development of prospective site – selection criteria
• Risk assessment, management and mitigation; delivery and risk focused
• Initiativeand critical thinking & planning ability
• Goodorganization, planning & communication skills
  
  

What Is Offered

• Solid structured on-boarding
• Full-time and permanent contract of employment with us seconded to one single sponsor
• Homebased in the UK/England
• Salary according to level of skills and experience
  
  

Why Join?

ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations.

With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life.

Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development.

At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best-in-class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.

At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know.

:

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Research, Analyst, and Information Technology

• Industries

  Pharmaceutical Manufacturing

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