Sr. Clinical Research Associate

Icon Clinical Plc; Milano; In loco; EUR 75.000 - 110.000; Tempo pieno

Vantaggi offerti da questo lavoro

Competitive base salary

Health, dental and vision coverage

Pension plans

Descrizione del lavoro

ICON Plc is seeking a Senior Clinical Research Associate (CRA) to oversee clinical trial activities in Milan, Italy. You will monitor sites, ensure protocol adherence, and support trial execution while maintaining data integrity and participant safety.

The role requires an advanced life sciences degree and extensive CRA experience, with travel up to 60% to domestic and international sites. Strong regulatory knowledge and cross-functional collaboration are essential.

Competenze

• Advanced degree in life sciences, nursing, or medicine.
• Extensive experience as a Clinical Research Associate with knowledge of GMP/GCP.
• Ability to manage multiple sites and projects and solve problems.

Mansioni

• Monitoring clinical trial sites to ensure adherence to protocols and GCP.
• Conducting site visits to assess performance and resolve issues.
• Collaborating with cross-functional teams to ensure accurate data collection and reporting.
• Providing training to site staff and other CRAs to maintain standards.
• Building relationships with site personnel to facilitate trial operations.

Conoscenze

Extensive CRA experience

Site monitoring

Regulatory compliance

Data integrity

Formazione

Advanced degree in life sciences

Descrizione del lavoro

Sr. Clinical Research AssociateICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.We are currently seeking a Senior Clinical Research Associate (CRA) to join our diverse and dynamic team. As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. You will contribute to the success of clinical trials by ensuring data integrity, participant safety, and compliance throughout the study lifecycle.

What You Will Be Doing:

• Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
• Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
• Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.
• Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
• Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.

Your Profile:

• Advanced degree in a relevant field such as life sciences, nursing, or medicine.
• Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.
• Proven ability to manage multiple sites and projects simultaneously, with strong organisational and problem-solving skills.
• Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.
• Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.
• Ability to travel at least 60% of the time (international and domestic – fly and drive) and should possess a valid driver’s license.
• Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Rewards Benefits:

• 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.

Are you a current ICON Employee?

SummaryLocation: Italy, MilanType: Full time

Sr. Clinical Research Associate • milan, lombardy, Italy