Senior Clinical Research Associate — Hybrid Trial Monitoring

CTI Clinical Trial and Consulting Services; Covington (KY); In loco; USD 70.000 - 95.000; Tempo pieno

Vantaggi offerti da questo lavoro

Hybrid work from home

Health benefits

Paid parental leave

Tuition reimbursement

Descrizione del lavoro

CTI Clinical Trial and Consulting Services is seeking a Clinical Trial Monitor to act as the primary CTI contact for assigned study sites across monitoring activities. You will conduct PSV, SIV, IMV, and COV visits, ensure regulatory compliance, and support start-up activities, site selection, and data/document tracking.

The role involves working with regulatory affairs, project teams, and site staff to ensure high-quality study execution and timely deliverables.

Competenze

• 1 year of clinical trial monitoring experience or equivalent.
• Bachelor's degree or higher in an allied health field or RN with an Associatea0Degree, or 3-year Nursing Diploma with at least 2 years clinical nursing experience.
• Previous experience in conducting clinical research studies in a hospital setting, pharmaceutical company, or CRO.
• Minimum 1 year of on-site monitoring experience preferred.

Mansioni

• Serve as main CTI contact for assigned study sites.
• Conduct site visits (PSV/SIV/IMV/COV) and complete visit deliverables within timelines.
• Assist with study start-up activities including feasibility and site selection.
• Collect, review, and track essential/regulatory documents.
• Participate in investigator, client, and project team meetings.
• Create and implement subject enrollment strategies for sites.
• Ensure storage, dispensation, and accountability of Investigational Product and materials.
• Perform site management activities and update the Clinical Project Manager.

Conoscenze

Clinical trial monitoring

Communication skills

Regulatory knowledge

Team collaboration

Formazione

Bachelor's degree in allied health field

Nursing background or RN with associate degree

3-year Nursing Diploma with 2 years nursing experience

Descrizione del lavoro

CTI Clinical Trial and Consulting Services is seeking a Clinical Trial Monitor to act as the primary CTI contact for assigned study sites across monitoring activities. You will conduct PSV, SIV, IMV, and COV visits, ensure regulatory compliance, and support start-up activities, site selection, and data/document tracking.

The role involves working with regulatory affairs, project teams, and site staff to ensure high-quality study execution and timely deliverables.