About the Role
This is a full-time, on-site position that requires a Sub-Investigator to support clinical research studies by ensuring protocol compliance, conducting study assessments, and monitoring participant safety.
The successful candidate will be responsible for collecting and analyzing data, managing investigational products, collaborating with the site team, and maintaining regulatory documentation.
Key Responsibilities:
* Data Collection: Gather and review participant information, medical history, and other relevant data as required by the study protocols.
* Investigational Products: Manage and maintain inventory of investigational products, ensuring proper handling, storage, and dispensing.
* Collaboration: Work closely with the site team, including researchers, coordinators, and other healthcare professionals, to ensure seamless execution of clinical trials.
* Regulatory Compliance: Maintain accurate and up-to-date records, adhere to Good Clinical Practice (GCP) guidelines, and ensure compliance with all applicable regulations and laws.
Requirements:
* Clinical Skills: Proven experience in patient assessment, data collection, and monitoring participant safety.
* Regulatory Knowledge: In-depth understanding of clinical trial protocols, documentation standards, and regulatory requirements.
* Communication: Excellent communication and teamwork skills to effectively collaborate with researchers, participants, and the clinical team.
* Attention to Detail: Strong analytical and problem-solving skills, with attention to detail for data review and investigational product management.
* Qualifications: Medical degree, nursing qualifications, or equivalent healthcare education and certification.