myGwork - LGBTQ+ Business Community
Senior CRA - Central/West/East - Remote
ICON plc is a leading healthcare intelligence and clinical research organization committed to fostering an inclusive environment that drives innovation and excellence. Join us in shaping the future of clinical development.
We are seeking a
Senior Clinical Research Associate (CRA)
to join our diverse team. As a Senior CRA, you will oversee and manage clinical trial activities to ensure compliance with protocols, regulatory standards, and industry guidelines. Your role is vital in maintaining data integrity, participant safety, and overall study success. Responsibilities include: Monitoring clinical trial sites for adherence to protocols, GCP, and regulatory requirements. Conducting site visits to evaluate performance, resolve issues, and support trial progress. Collaborating with cross-functional teams for accurate data collection and reporting. Providing training and guidance to site staff and fellow CRAs. Building relationships with site personnel and stakeholders for smooth operations. Qualifications: Advanced degree in life sciences, nursing, medicine, or related field. Extensive experience as a Clinical Research Associate with strong knowledge of clinical trial processes. Based in the Central, West, or East regions. At least 3 years of independent monitoring experience. Ability to manage multiple sites and projects with excellent organizational skills. Proficiency in monitoring practices, data integrity, site management, and relevant software. Strong communication, interpersonal, and stakeholder management skills. Therapeutic Areas:
Oncology - Solid Tumor; General Medicine - Vaccines, NASH/MASH, Cardio, Diabetes. What ICON Offers: A diverse culture that rewards high performance and nurtures talent. Competitive salary and benefits focused on well-being and work-life balance. Benefits include annual leave, health insurance, retirement plans, 24/7 Employee Assistance, life assurance, and flexible benefits. Visit our
careers site
to learn more about our benefits. ICON values inclusion and belonging, providing an accessible environment free from discrimination. We encourage all qualified candidates to apply, regardless of background or disability. If you require accommodations during the application process, please let us know or submit a request
here . Interested but unsure if you meet all requirements? We encourage you to apply—your skills might be exactly what we need. Current ICON employee? Apply
here .
#J-18808-Ljbffr
Senior Clinical Research Associate (CRA)
to join our diverse team. As a Senior CRA, you will oversee and manage clinical trial activities to ensure compliance with protocols, regulatory standards, and industry guidelines. Your role is vital in maintaining data integrity, participant safety, and overall study success. Responsibilities include: Monitoring clinical trial sites for adherence to protocols, GCP, and regulatory requirements. Conducting site visits to evaluate performance, resolve issues, and support trial progress. Collaborating with cross-functional teams for accurate data collection and reporting. Providing training and guidance to site staff and fellow CRAs. Building relationships with site personnel and stakeholders for smooth operations. Qualifications: Advanced degree in life sciences, nursing, medicine, or related field. Extensive experience as a Clinical Research Associate with strong knowledge of clinical trial processes. Based in the Central, West, or East regions. At least 3 years of independent monitoring experience. Ability to manage multiple sites and projects with excellent organizational skills. Proficiency in monitoring practices, data integrity, site management, and relevant software. Strong communication, interpersonal, and stakeholder management skills. Therapeutic Areas:
Oncology - Solid Tumor; General Medicine - Vaccines, NASH/MASH, Cardio, Diabetes. What ICON Offers: A diverse culture that rewards high performance and nurtures talent. Competitive salary and benefits focused on well-being and work-life balance. Benefits include annual leave, health insurance, retirement plans, 24/7 Employee Assistance, life assurance, and flexible benefits. Visit our
careers site
to learn more about our benefits. ICON values inclusion and belonging, providing an accessible environment free from discrimination. We encourage all qualified candidates to apply, regardless of background or disability. If you require accommodations during the application process, please let us know or submit a request
here . Interested but unsure if you meet all requirements? We encourage you to apply—your skills might be exactly what we need. Current ICON employee? Apply
here .
#J-18808-Ljbffr