Global Clinical Research Associate (Remote/Travel)

Syneos Health, Inc.; Oklahoma City (OK); Vor Ort; USD 70.000 - 110.000; Vollzeit

Benefits dieser Stelle

Company car/allowance

Health benefits (Medical, Dental, VIs

401k with company match

Employee Stock Purchase Plan

Performance bonus

Paid time off

Zusammenfassung

Syneos Health is seeking an Experienced Clinical Research Associate to regionally support US sites. You will conduct site qualification, monitoring, and regulatory compliance tasks, ensuring data integrity and patient safety throughout trials.

This role requires extensive travel (up to 75%) and collaboration with cross-functional teams to meet study milestones and quality standards. A strong clinical development background is essential for success.

Qualifikationen

• 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.
• Ability to manage required travel of up to 75% on a regular basis.

Aufgaben

• Performs site qualification, initiation, interim monitoring, site management and close-out visits (on-site or remote) ensuring regulatory, ICH-GCP and/or GPP compliance.
• Verifies informed consent processes and protects patient confidentiality while assessing safety and data integrity factors.
• Performs source data review, data entry checks, and drives query resolution to closure.
• May manage IP inventory, labeling, and storage compliance according to protocol.

Kenntnisse

Site monitoring

ICH-GCP knowledge

Regulatory compliance

Communication skills

Travel readiness

Ausbildung

Bachelor's degree or RN

Jobbeschreibung

Syneos Health is seeking an Experienced Clinical Research Associate to regionally support US sites. You will conduct site qualification, monitoring, and regulatory compliance tasks, ensuring data integrity and patient safety throughout trials.

This role requires extensive travel (up to 75%) and collaboration with cross-functional teams to meet study milestones and quality standards. A strong clinical development background is essential for success.