JD-836 CLINICAL RESEARCH ASSISTANT

Neutra Life Sciences


Job Description: Clinical Research Assistant Position: Clinical Research Assistant Location: Remote Employment Type: Full-Time (40 hours per week) Reporting To: Director of Clinical Operations Job Summary The Clinical Research Assistant will play a crucial role in supporting clinical research by accurately inputting medical data, coordinating patient follow-ups, and assisting in recruitment efforts. This position requires a bilingual (English/Spanish) healthcare professional with a strong foundation in medical research practices and GCP certification. Key Responsibilities - Data Management: - Input and maintain high-quality, confidential medical data for clinical research studies. - Ensure data accuracy and compliance with study protocols and regulatory standards. - Patient Engagement: - Make outbound phone calls to patients for follow-up and recruitment. - Provide clear communication and support to patients regarding study procedures. - Collaboration: - Work closely with the Clinical Operations Director and research team to coordinate study activities. - Assist with scheduling and administrative tasks as needed. - Compliance: - Adhere strictly to Good Clinical Practice (GCP) guidelines and all applicable regulatory requirements. - Maintain thorough and up-to-date records of patient interactions and study progress. Qualifications - Residency: Must reside in Colombia. - Language: Proficient in both English and Spanish. - Education & Experience: - Background in healthcare (e.g., doctor, nursing, allied health, medical assistant, etc.) - Previous experience in clinical research or data management is preferred. - Certification: Must hold a current GCP certification. - Technical Skills: - Proficient in data entry and basic office software. - Comfortable with remote work tools and communication platforms. - Proficient in electronic medical records Skills & Competencies - Excellent attention to detail and organizational skills. - Strong verbal and written communication abilities. - Ability to work independently in a remote environment. - Demonstrated problem-solving skills and reliability. - Capable of managing multiple tasks and prioritizing effectively. Work Environment & Benefits - Remote Setup: - Must have reliable internet access and a quiet, dedicated workspace. - Schedule: - 40 hours per week with flexibility to manage patient follow-ups. - Compensation: - Competitive salary commensurate with experience. - Additional benefits may be available based on company policies. Application Process - Interested candidates should submit: - A resume highlighting relevant healthcare or research experience. - A cover letter detailing why they are a strong fit for the role. - Proof of current GCP certification. Job Type: Full-time Application Question(s): - Can you describe your experience auditing or reviewing medical records? - Which Electronic Data Capture (EDC) systems have you worked with, and what was your role utilizing these systems? Education: - Bachelor's (Required) License/Certification: - Good Clinical Practice (GCP) (Required) Application Deadline: 01/03/2025

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