Dozee is a leading healthcare technology company specializing in remote patient monitoring solutions. With a mission to improve patient care through innovative technologies, Dozee combines advanced medical devices with data analytics to empower healthcare professionals. Based in Vellore, Tamil Nadu, the company is committed to conducting high-quality clinical studies that drive the development of its groundbreaking products. Join us as we embark on a journey to redefine patient care and enhance clinical outcomes.
Responsibilities in Job
As a Clinical Research Associate (Contract, On-site) at Dozee, your key responsibilities will include:
- Study Execution: Assist in conducting clinical studies in compliance with the study protocol and regulatory standards, ensuring adherence to Good Clinical Practice (GCP) guidelines.
- Patient Management: Support the recruitment, screening, and enrollment of study participants. Guide participants through the informed consent process, ensuring they understand study procedures.
- Data Collection: Collect accurate clinical data from participants, documenting all information in study records and conducting source data verification to maintain data integrity.
- Shift Coverage: Work both day and night shifts to ensure continuous monitoring and data collection in accordance with the study protocol.
- Protocol Adherence: Monitor patient care and assist with troubleshooting any study-related issues to ensure protocol adherence.
- Regulatory Compliance: Maintain up-to-date study documentation that meets regulatory and sponsor requirements.
- Communication: Act as a liaison between investigators, study participants, and the research team, facilitating clear communication of study updates and issues.
- Supervision: Report directly to the Clinical Research Associate, providing updates and ensuring smooth operations throughout the study.
Qualifications
To be considered for the Clinical Research Associate position at Dozee, candidates should possess the following qualifications:
- A Bachelor’s degree in life sciences, biomedical engineering, biotechnology, health sciences, pharmacy, or a related field.
- Experience: 0-1 year of experience in clinical or academic research is preferred. Fresh graduates with relevant qualifications are encouraged to apply.
Skills
Successful candidates will demonstrate the following skills:
- Clinical Research: Familiarity with clinical trial processes and regulatory requirements.
- Communication: Strong communication skills to effectively interact with study staff, participants, and investigators.
- Data Collection: Attention to detail and accuracy in collecting and documenting clinical data.
- Organizational Skills: Ability to manage multiple tasks effectively and work independently.
- Collaboration: Strong team player with a willingness to work flexible hours, including day and night shifts.
