Clinical Research Associate

About ScriptPro BioTech

ScriptPro BioTech is an expanding biotechnology company dedicated to advancing clinical research and innovative therapeutic approaches. Collaborating closely with healthcare providers, research institutions, and industry stakeholders, the organization ensures execution of high-standard clinical trials emphasizing data accuracy, patient safety, and compliance with regulatory standards. The team environment is supportive and collaborative, fostering scientific rigor and ongoing learning opportunities. Employees contribute to impactful studies aimed at enhancing patient outcomes and influencing future medical therapies.

Position Overview

The Clinical Research Associate (CRA) will operate remotely in a full-time capacity, responsible for overseeing clinical trial processes to guarantee compliance with study protocols, Good Clinical Practice (GCP), and regulatory frameworks. Daily activities include reviewing documentation, validating source data, and ensuring precise, prompt data entry at study sites. The CRA liaises with site personnel, investigators, and internal clinical teams to manage study initiation, ongoing monitoring, and study closure. Additional responsibilities involve drafting monitoring reports, identifying and resolving protocol discrepancies, conducting risk analyses, and contributing to quality enhancement efforts. The role requires active participation in team communications and provision of training support to site staff as necessary.

Qualifications

• In-depth knowledge of clinical trial protocols and ability to maintain protocol compliance at multiple sites.
• Prior experience as a Clinical Research Associate or equivalent clinical trial monitoring role.
• Familiarity with clinical trial processes including study start-up, monitoring, and closure.
• Competence in clinical research operations adhering to GCP, ICH guidelines, and regulatory mandates.
• Bachelor’s degree in life sciences, nursing, pharmacy, or related disciplines; advanced clinical research degrees or certifications are advantageous.
• Strong organizational, analytical, and problem-solving capabilities with meticulous attention to data quality.
• Effective verbal and written communication skills enabling collaboration with diverse and remote teams.
• Comfortable working remotely using electronic data capture systems and digital collaboration tools.
• Experience in biotech, pharmaceutical, or medical device clinical research is a plus.

Compensation

The annual salary range is from $115,000 to $125,000.