Senior Regional Clinical Research Lead - MedTech Trials

Kelly Science, Engineering, Technology & Telecom; Chicago (IL); Sur place; USD 75 000 - 105 000; Plein temps

Avantages offerts par ce poste

Medical insurance

Dental insurance

Vision insurance

401K

Paid time off

Résumé du poste

Kelly Science and Clinical FSP is seeking a Regional Clinical Research Associate for a long-term engagement in the US with a MedTech client. As a Kelly FSP employee, you will receive comprehensive benefits including medical, dental, vision, 401K, and PTO.

The candidate will manage clinical activities at study sites, monitor site performance, ensure data quality, and maintain regulatory compliance across projects.

Qualifications

• Bachelor's degree is required.
• 4–5 years of relevant clinical research experience; Masters/PhD/MD/PharmD with at least 3 years also acceptable.
• Experience in medical device monitoring or equivalent.
• Understanding of regulations and standards in clinical research and medical devices.
• Relevant industry certifications preferred.

Responsabilités

• Manage clinical study activities at multiple sites across projects.
• Oversee site performance and ensure data quality and timeliness.
• Coordinate site visits, monitoring, and communications with site personnel.
• Ensure compliance with study protocol, SOPs, GCP, and regulatory requirements.
• Support site recruitment and retention activities.
• Interface with Investigators, IRBs/ECs, vendors, and internal stakeholders.
• Maintain Investigator Site Files per regulations.
• Assist with training meetings and dissemination of important data.

Connaissances

Clinical research experience

Medical device monitoring

Regulatory knowledge

Site management

Vendor coordination

Formation

Bachelor's degree

Master's degree / PhD / MD / PharmD

Description du poste

Kelly Science and Clinical FSP is seeking a Regional Clinical Research Associate for a long-term engagement in the US with a MedTech client. As a Kelly FSP employee, you will receive comprehensive benefits including medical, dental, vision, 401K, and PTO.

The candidate will manage clinical activities at study sites, monitor site performance, ensure data quality, and maintain regulatory compliance across projects.