Origin Medical Research Lab, the research division of Origin Medical, operates at the intersection of artificial intelligence (AI) and healthcare to drive advancements in maternal health. Headquartered in Cambridge, Massachusetts, USA, Origin Medical aims to improve prenatal care and ensure maternal health equity worldwide, using AI-powered solutions.

The lab is committed to developing products that enable healthcare professionals in rural and urban areas to deliver timely, effective interventions. With a focus on reducing maternal and infant mortality rates, Origin Medical Research Lab fosters a work culture that promotes collaboration, growth, and ownership. They are looking for talented individuals passionate about clinical research and healthcare innovation to join their mission-driven team in Bengaluru.

Job Responsibilities of a Clinical Research Analyst

As a Clinical Research Analyst at Origin Medical Research Lab, your role will involve close collaboration with regulatory affairs teams, clinicians, AI experts, and clinical trial experts to manage and execute clinical studies. Your primary tasks will include:

1. Clinical Study Design and Management:
   • Coordinate with clinical investigators and contract research organizations (CROs).
   • Conduct clinical studies, analyze research data, and assess outcomes.
   • Perform statistical assessments to benchmark product safety and efficacy.
2. Ensure Technology Safety & Efficacy:
   • Liaise with clinicians and internal teams to ensure the product meets clinical safety standards.
   • Prepare datasets for clinical studies to monitor effective product development.
3. Clinical Site Management:
   • Identify and set up clinical trial sites, including staff training.
   • Monitor trial sites regularly to ensure medical and scientific compliance.
4. Technical Documentation and Writing:
   • Prepare clinical trial documentation, including ethics board applications and trial reports.
   • Document changes in Good Clinical Practices (GCP) and update device regulations.
5. Regulatory and Compliance Documentation:
   • Maintain accurate regulatory documentation and clinical trial records.
   • Stay updated with clinical regulations to ensure full compliance.
6. Collaboration with Investigators and Research Teams:
   • Liaise with investigators to ensure smooth trial execution.
   • Develop strategies for researching comparable medical devices in the market.

Qualifications and Requirements

To succeed in this role, candidates must meet the following qualifications and requirements:

• Education & Experience:
  • Experience in clinical research, trials management, and technical writing But Not Mandatory
  • Familiarity with medical devices and regulatory standards (e.g., FDA).
  • Knowledge of statistical tools such as SPSS, R, or Python is a plus.
• Skills:
  • Strong research and documentation abilities.
  • Excellent verbal and written communication skills.
  • Ability to manage multiple projects and deadlines efficiently.
  • Problem-solving mindset with ethical project management skills.
  • Passion for healthcare innovation, particularly in AI-driven prenatal care.

Key Skills Required

• Clinical trials and studies management
• Technical writing and research documentation
• Strong communication and collaboration abilities
• Knowledge of GCP and regulatory guidelines
• Familiarity with Microsoft 365 applications and statistical tools

Application Link