-Global Study Manager (GSM), CVRM

Remote Worker LTD.; United States; Teletrabalho; USD 93 000 - 146 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

Competitive base salary

Wellbeing programmes

Retirement and pension plans

Life assurance and disability

Training and career development

Resumo da oferta

ICON Strategic Solutions is seeking a Global Study Manager to lead and deliver global clinical studies from protocol to close-out, coordinating with cross-functional teams, CROs, and vendors to ensure high quality, on-time results and regulatory compliance. The role focuses on cardiovascular programmes and global trial execution across geographies.

The successful candidate will bring life sciences expertise, 3+ years in global trial management, and strong stakeholder communication, working in a

Qualificações

• Degree in Life Sciences, Medical Sciences, Biological Sciences or related field.
• 3+ years global trial management experience in clinical research, pharma or CRO.
• Strong understanding of clinical development and drug development process.
• Excellent knowledge of ICH-GCP and global trial regulations.
• Proven project management and organisational skills.
• Strong stakeholder management and communication skills.
• Experience in global cross-functional teams.
• Cardiovascular trials experience desirable.

Responsabilidades

• Support delivery of global clinical studies from protocol development to close-out and archiving.
• Collaborate with internal stakeholders, CROs and external vendors globally.
• Ensure studies are delivered on time, within budget, and with high quality and compliance.
• Contribute to innovative programmes, including cardiovascular trials.

Conhecimentos

Global trial management

Stakeholder management

Cross-functional teamwork

Communication skills

Independent working

Formação académica

Life sciences degree

Descrição da oferta de emprego

Senior Project Manager UK

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.

About the Role

Our client is seeking a talented Global Study Manager to support the delivery of global clinical studies from protocol development through study close-out and archiving.

Working as part of a cross-functional global study team, you will collaborate with internal stakeholders, CROs, and external vendors on a global level to ensure studies are delivered on time, within budget, and to the highest quality and compliance standards. The successful candidate will have the opportunity to support innovative programmes, including global cardiovascular clinical trials focused on advancing treatments for patients with cardiovascular disease.

About You

• Degree qualified in Life Sciences, Medical Sciences, Biological Sciences, or a related field.


• UK based, with 3+ years of Global trial management experience in clinical research, pharmaceutical development, biotechnology, or a CRO environment.


• Strong understanding of clinical development and the drug development process.


• Excellent knowledge of ICH-GCP and global clinical trial regulations.


• Proven project management and organisational skills.


• Strong stakeholder management and communication skills.


• Experience working effectively within global, cross-functional teams.


• Previous experience supporting cardiovascular clinical trials is highly desirable.


• Proactive, collaborative, and able to work independently in a fast-paced environment.

Why Apply?

This is an exciting opportunity to join a leading organisation and contribute to the delivery of innovative clinical research programmes. You'll play a key role in global studies, including those within the cardiovascular therapeutic area, helping advance potential new treatments for patients living with cardiovascular disease worldwide.

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.