Company Description
We are patient-centric organization that brings together clinicians, therapeutic area subject matter experts, and bio-pharma organizations to advance medical science. We focus on conducting faster, more efficient, and high-quality clinical trials. Our mission is to bridge the gap between research and care, ensuring better outcomes for patients. Through collaboration and innovation, we are committed to driving scientific discoveries forward.
Role Description
This is a full-time, on-site role for a Clinical Research Coordinator. The Clinical Research Coordinator will oversee and manage clinical research studies, ensuring compliance with protocols and regulations. Responsibilities include obtaining informed consent from participants, working closely with investigators on study protocols, coordinating day-to-day operations of clinical trials, and maintaining accurate research data and records. The role also involves collaborating with cross-functional teams and monitoring the progress of studies to ensure quality and efficiency. As a part of this role you will be assigned to site/s and you will work from there when needed.
Qualifications
- Minimum 1 year of Clinical Research Experience Required
- Proficiency in obtaining Informed Consent and thorough understanding of Protocol guidelines
- Solid experience in Research and Clinical Research methodologies
- Hands-on experience with Clinical Trials and familiarity with related processes
- Strong organizational and communication skills
- Ability to comply with regulatory requirements and ethical guidelines
- Bachelor's degree in a related field or equivalent experience
- Certification in clinical research coordination is a plus
