Senior Clinical Research Associate- Early Development
Behavioral Health Market Context
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Job Description
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 organizational 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.
• Must be located in the LA or SF Bay area
• Five years of CRA experience with phase I oncology monitoring experience
• Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid drivers license
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 organizational 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.
• Must be located in the LA or SF Bay area
• Five years of CRA experience with phase I oncology monitoring experience
• Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid drivers license
Qualifications
- •4+ years of CRA experience at a CRO
- •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 organizational 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
- •Must be located in the LA or SF Bay area
- •Five years of CRA experience with phase I oncology monitoring experience
- •Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid drivers license
Benefits
Responsibilities
- •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
- •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
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