Remote CRA II - Sponsor-Dedicated Monitoring

Syneos Health, Inc.; Minnesota; Hybrid; USD 80,000 - 110,000; Full time

Benefits offered by this job

Health benefits

Paid time off

Job summary

Syneos Health is seeking an Experienced Clinical Research Associate - Sponsor Dedicated to join our team. The role involves monitoring clinical sites remotely, ensuring regulatory and protocol compliance, and supporting study delivery for sponsor partnerships.

Qualified candidates have a bachelor’s degree or RN in a related field, knowledge of GCP/ICH guidelines, strong communication and computer skills, and willingness to travel up to 75% of the time.

Qualifications

• Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements.
• Excellent communication, presentation and interpersonal skills.
• Must demonstrate good computer skills and be able to embrace new technologies.
• Ability to travel up to 75% on a regular basis.

Responsibilities

• Performs site qualification, initiation, interim monitoring and close-out visits, on-site or remotely, ensuring regulatory and protocol compliance.
• Verifies informed consent processes and protects subject confidentiality and data integrity.
• Assesses site processes, conducts Source Document Review, and drives query resolution to closure.
• Manages IP inventory, storage, labeling, and regulatory compliance for investigational products.
• Maintains ISF and TMF accuracy and archiving per regulations.
• Documents activities and supports recruitment, retention and data tracking.
• Understanding project scope, budgets, timelines; communication to ensure objectives are met.

Skills

GCP knowledge

Communication

Computer skills

Travel up to 75%

Education

Bachelor’s degree or RN in a related field or equivalent combination of education, training and experience

Job description

Syneos Health is seeking an Experienced Clinical Research Associate - Sponsor Dedicated to join our team. The role involves monitoring clinical sites remotely, ensuring regulatory and protocol compliance, and supporting study delivery for sponsor partnerships.

Qualified candidates have a bachelor’s degree or RN in a related field, knowledge of GCP/ICH guidelines, strong communication and computer skills, and willingness to travel up to 75% of the time.