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Clinical Research Lead

Role overview

Qualifications

  • BA / BS/ BSc in the sciences or RN
  • Experience in oversight of external vendors (CROs, central labs, imaging vendors, etc.)
  • Strong interpersonal and communication skills
  • Knowledge of ICH-GCP guidelines and regulatory requirements for clinical trials

Responsibilities

  • Management of clinical Investigators and sites participating in clinical trials
  • Timely delivery of clinical trial enrollment in accordance with scientific objectives
  • Oversight of vendor monitoring activities at clinical trial sites
  • Ensuring inspection readiness at all times for assigned therapeutic areas

Key facts

  • Remote from: United Kingdom
  • Full time
  • Senior (5-10 years)
  • Clinical Research Coordinator
  • English

Hard skills

Other skills

  • Social Skills
  • Verbal Communication Skills
  • Problem Solving
  • Organizational Skills
  • Time Management

About the company

ICON plc logo

ICON plc

Contract Research Organizations (CRO)

Since our foundation in Dublin, Ireland in 1990, our mission has been to help our clients to accelerate the development of drugs and devices that save lives and improve quality of life. We do this by delivering best in class information, solutions and performance, with an unyielding focus on quality at all times. We offer a full range of consulting, development and commercialisation services from a global network of offices in 53 countries. We focus our innovation on the factors that are critical to our clients – reducing time to market, reducing cost, and increasing quality – and our global team of experts has extensive experience in a broad range of therapeutic areas.

Company details

Company typeXLarge
IndustryContract Research Organizations (CRO)
Company size10001

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Job description

A great role for an autonomous Senior CRA to perform hybrid Lead CRA/Junior management tasks

At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.


As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.


Clinical Research Lead (client working title) homebased UK

You will contribute to clinical research activities, taking responsibility for your deliverables and working collaboratively. The role involves stakeholder management role and strong interpersonal skills

What You Will Do:

The Clinical Research Lead (CRL) is responsible for the management of clinical Investigators and sites being considered and/or participating in the client’s clinical trials and / or Post Marketing Safety Studies; inclusive of Investigator / site identification and qualification, the timely delivery of clinical trial enrollment in accordance with scientific objectives, timely delivery of database locks, issues management at clinical trial sites, and ensuring inspection readiness at all times for assigned therapeutic area(s) that enables global program delivery. This is achieved by the CRL’s accountability for comprehensive Investigator and site management, leveraging of information/tools to make/have informed decisions and discussions, and high-quality interactions with global clinical trial sites to drive to an unparalled customer experience. The CRL is also responsible for oversight of vendor monitoring activities at clinical trial sites, including the identification, mitigation and escalation of significant findings and trends.

What is required

• BA / BS/ BSc in the sciences or RN is required and preferred

• Experience in oversight of external vendors (CROs, central labs, imaging vendors, etc.)

• Strong investigator-sponsored study experience gained within the industry at a clinical trial manager level.

• Influential and effective communication skills

• Energetic, flexible work approach as very autonomous role – good ability to think outside of the box

• Previous experience gained in a biotech, pharmaceutical or CRO company is preferred

• Travel on average 6 times per month

• Valid and current UK working eligibility

Your Profile:

You will bring relevant experience as a Senior CRA (Clinical Research Associate), along with the following qualifications and skills.

• Bachelor's degree in life sciences or a related field.

• Previous experience in clinical research, site management, or a related field preferred.

• Strong interpersonal and communication skills, with the ability to build rapport and establish effective working relationships with diverse stakeholders.

• Excellent organizational and problem-solving skills, with the ability to prioritize and manage multiple tasks simultaneously.

• Knowledge of ICH-GCP guidelines and regulatory requirements for clinical trials.

#LI-Remote:

#LI-ET1


Employment with ICON is contingent upon having the legal right to work in the country where the role is based.


Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.


Benefits may include:

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.


Visit our careers site to read more about the benefits ICON offers.


Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.


If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.


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Marcus Rivera

Chief Revenue Officer

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