Senior CRA — Remote Site Monitoring & Study Leadership

Syneos Health, Inc.; Finland; On-site; EUR 65,000 - 90,000; Full time

Job summary

Syneos Health, Inc. is seeking a Senior Clinical Research Associate I to support site qualification, initiation and monitoring visits, ensuring GCP and regulatory compliance across projects.

You will verify informed consent, review ISF/TMF, and manage data quality while coordinating with site staff and sponsor teams. You will travel up to 75% regularly, train junior CRAs, and participate in Investigator Meetings and site audits as needed.

Qualifications

• Bachelor’s degree or RN in a related field or equivalent combination of education, training and experience.
• Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements.
• Must demonstrate good computer skills and be able to embrace new technologies.
• Excellent communication, presentation and interpersonal skills. Basic level of critical thinking skills expected.
• Ability to manage required travel of up to 75% on a regular basis

Responsibilities

• Performs site qualification, site initiation, interim monitoring, site management and close-out visits (performed on-site or remotely) ensuring regulatory, ICH-GCP and/or Good Pharmacoepidemiology Practice (GPP) and protocol compliance.
• Verifies informed consent and documents appropriately; protects subject confidentiality and data integrity.
• Conducts Source Document Review of site source documents and medical records; verifies CRF data accuracy.
• Applies query resolution remotely and on-site, guiding site staff to closure within timelines.
• Utilizes hardware and software to support study data review and capture; ensures IP inventory, labeling and approvals.
• Prepares for Investigator Meetings; participates in sponsor meetings and training sessions as required.
• Provides training or mentorship to junior CRAs; may lead tasks under supervision; collaborates with RWLP regulatory teams.

Skills

Communication skills

Interpersonal skills

Critical thinking

Computer skills

Travel readiness

Education

Bachelor’s degree or RN

Job description

Syneos Health, Inc. is seeking a Senior Clinical Research Associate I to support site qualification, initiation and monitoring visits, ensuring GCP and regulatory compliance across projects.

You will verify informed consent, review ISF/TMF, and manage data quality while coordinating with site staff and sponsor teams. You will travel up to 75% regularly, train junior CRAs, and participate in Investigator Meetings and site audits as needed.