Clinical Trial Manager

Regulatory Toolkit; Center Square (PA); Sur place; USD 90 000 - 130 000; Plein temps

Avantages offerts par ce poste

Health benefits

Retirement plan

Life insurance

Employee assistance program

Career development

Résumé du poste

ICON Strategic Solutions is seeking a Clinical Trial Manager to oversee day-to-day trial management activities for Phase I studies. You will support your team and stakeholders to ensure high-quality outcomes across clinical programmes.

The role requires a university degree in medicine or science and a minimum of three years' industry trial management experience, including Phase I studies. Some travel may be required, and employment is contingent on legal work authorization.

Qualifications

• Bachelor-level degree or higher in medicine, science, or equivalent combination of education and experience.
• Minimum of three years of industry clinical trial management experience.
• Proven ability to drive clinical deliverables of a study.
• Experience managing Phase I (healthy volunteer) studies.

Responsabilités

• Plan and manage all aspects of clinical trials, including timelines, budget, and quality.
• Collaborate with cross-functional teams to implement protocols and procedures.
• Build and manage relationships with investigators and stakeholders.
• Ensure trials comply with local, national, and international regulations and ethics guidelines.
• Assess risks, make decisions on trial design, vendor selection, and risk management.

Connaissances

Clinical trial management

Team leadership

Regulatory compliance

Cross-functional collaboration

Formation

University degree in medicine or science

Description du poste

Clinical Trial Manager - Phase I

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.

As a Clinical Trial Manager at ICON, you will manage clinical trial operations activities, supporting your team and stakeholders to deliver high-quality outcomes across our clinical programmes.

What You Will Do:

You will manage day-to-day clinical trial management activities, supporting your team to deliver quality outcomes.
Key responsibilities include:

• Plan and manage all aspects of clinical trials, ensuring adherence to timelines, budget, and quality standards.

• Collaborate with cross-functional teams to establish and implement clinical trial protocols and procedures.

• Build and manage strong relationships with trial investigators and stakeholders.

• Ensure all trials are conducted in compliance with local, national, and international regulations and ethical guidelines.

• Problem-solve and make critical decisions regarding trial design, vendor selection, and risk management.

Your Profile:

You will have solid clinical trial management experience, with the ability to manage competing priorities and develop your team.
Required qualifications and experience:

• University degree in medicine, science, or equivalent combination of education & experience.

• A minimum of three years of industry clinical trial management experience

• Demonstrated ability to drive the clinical deliverables of a study

• Experience managing phase I (healthy volunteer) studies

• Some travel may be required

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.

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.