Clinical Research Analyst
24 hours ago
At Origin Medical Research Lab, we are seeking a highly motivated Clinical Research Analyst to join our team. As a Clinical Research Analyst, you will play a key role in planning, designing, and executing clinical studies and trials required for FDA clearance of our flagship product. You will work closely with the Regulatory Affairs team, renowned regulatory and clinical trial experts, and consultants to ensure adherence to international regulations and guidelines.
Key Responsibilities:
Conduct clinical studies by coordinating with clinical principal investigators and contract research organizations.
Coordinate with the research team to analyze clinical data and results from the study team to benchmark and perform appropriate statistical assessments.
Liaise with clinicians, internal team comparison of data engineers, and research engineers for preparing appropriate datasets for clinical studies to ensure the safety and effective functioning of the product.
Develop strategies to select the relevant clinical sites, setting up the trial sites, which includes training the site staff to trial-specific industry standards, monitoring the trial throughout its duration from a Medical/Scientific/Clinical perspective, which involves visiting the trial sites on a regular basis.
Prepare technical documents to support implementing good clinical practices, filing and collating trial documentation and reports, assisting in preparing clinical trial site ethics review board applications for investigational device trials, prepare interim or final reports for trial site ethics boards as required.
Requirements:
Highly motivated individuals looking for building a career in clinical research and trials that are essential to bringing any medical device out in the market for improving the lives of people and quality of care.
Individuals who are passionate about medical AI and are keen to work across all the teams during every stage of medical AI product development, to ensure the product's safety and effective functioning of the technology.
Detail-oriented individual who can efficiently design, manage, and conduct clinical studies.
Individual who is inquisitive and has the ability to self-learn new skills or techniques needed.
Good written and verbal communication skills with the ability to listen, articulate, and advocate.
Proactive, high-performance, result-oriented, and manage projects with ethical integrity.
Technical research and documentation skills (e.g. analyzing clinical research papers, preparing internal policies and documentation on Microsoft 365 applications).
Knowledge of statistical programming software and languages like SPSS, R, or Python is a plus.
What We Offer:
Competitive monthly compensation aligned with industry standards.
Comprehensive benefits package, including Provident fund, Paid annual leaves, Sick leaves, Wellness allowance, Insurance allowance.
Opportunity to work with an exceptional team of highly qualified individuals who strive towards a common goal of delivering a product that improves the standard of care for expecting mothers everywhere.
Collaborate with renowned clinicians, AI scientists, and business leaders from around the world.
Inclusive and optimistic company culture that places great value on collaboration, teamwork, and work-life balance.
Supportive environment where individuals genuinely care about each other's success and well-being.
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