Clinical Research Coordinator / Biomedical Research Analyst / Lab Operations Specialist

Clinical Research Coordinator

• Coordinate and manage clinical trials and research studies from initiation to completion
• Ensure study protocols are followed in compliance with regulatory requirements (GCP, IRB, ethics standards)
• Recruit, screen, and enroll eligible study participants
• Obtain informed consent and maintain participant documentation and records
• Schedule and coordinate patient visits, assessments, and follow-up procedures
• Collect, manage, and validate clinical trial data for accuracy and completeness
• Liaise with investigators, sponsors, hospitals, and regulatory bodies
• Monitor study progress, timelines, and protocol adherence
• Ensure patient safety and report adverse events or protocol deviations
• Support audit preparation and regulatory inspections

Biomedical Research Analyst

• Conduct scientific and biomedical research using laboratory and clinical data
• Analyze biological, medical, and experimental data using statistical and computational tools
• Support development of research hypotheses, study designs, and experimental methodologies
• Interpret research findings and prepare scientific reports, papers, and presentations
• Collaborate with scientists, clinicians, and research teams on biomedical studies
• Work with datasets from genomics, proteomics, or clinical trials depending on specialization
• Apply data analysis tools and techniques to identify patterns and insights
• Support grant writing and research proposal development
• Ensure research compliance with ethical and scientific standards

Lab Operations Specialist

• Manage daily operations of laboratory environments to ensure efficiency and compliance
• Oversee lab equipment maintenance, calibration, and inventory management
• Ensure proper handling, storage, and disposal of biological and chemical materials
• Maintain laboratory safety standards and regulatory compliance (GLP, ISO, etc.)
• Coordinate sample processing, tracking, and documentation workflows
• Support procurement of lab supplies, reagents, and consumables
• Train laboratory staff on SOPs, safety procedures, and equipment usage
• Ensure accurate record-keeping and quality control across lab processes
• Assist in audits, inspections, and quality assurance activities

• Bachelor's or Master's degree in Life Sciences, Biomedical Sciences, Biotechnology, Pharmacy, Medicine, or related field
• 2–8+ years of experience in clinical research, biomedical research, or laboratory operations roles
• Strong understanding of clinical trial processes, research methodologies, and laboratory procedures
• Knowledge of regulatory standards (GCP, GLP, FDA, EMA, IRB/ethics guidelines)
• Experience with data analysis tools and research software (SPSS, R, SAS, or similar) is a plus
• Strong analytical, documentation, and reporting skills
• Excellent attention to detail and organizational abilities
• Strong communication and collaboration skills with multidisciplinary teams
• Experience working in hospitals, research institutes, pharmaceutical, or biotech environments is preferred
• Familiarity with lab equipment, sample handling, and quality control procedures (for lab roles)
• Ability to work in highly regulated and detail-sensitive environments
• Strong problem-solving and critical thinking skills