Clinical Research Assistant

hace 2 semanas

Bogotá, Colombia Neutra Life Sciences A tiempo completo

**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**
- 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.

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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