BIOSPECIMEN SOLUTIONS PRIVATE LIMITED

You will be responsible for overseeing the day-to-day operations of clinical research studies at Biospecimen Solutions Pvt Ltd. This includes tasks such as obtaining informed consent, adhering to protocols, managing research activities, and ensuring compliance with clinical trial regulations. Key Responsibilities: - Coordinate the day-to-day operations of clinical research studies - Obtain informed consent from study participants - Follow protocols outlined for each research study - Manage various research activities as required - Ensure compliance with all clinical trial regulations Qualifications Required: - Possess skills in informed consent and protocol management - Previous experience in Clinical Research and Clinical Trials - Strong understanding of research methodologies - Familiarity with IRB/EC approval processes - Excellent organizational and communication skills - Ability to work both independently and collaboratively - Hold a Bachelor's degree in a related field (e.g., Life Sciences, Nursing, Pharmacy),