What are the responsibilities and job description for the Clinical Research Associate position at ClinDatrix, Inc.?
Company Description
ClinDatrix, Inc. is a privately held, full-service contract research organization (CRO) founded in 2002 to support drug and medical device innovators in navigating the development and regulatory approval processes. The company offers expertise from preclinical development to regulatory filings and post-marketing studies. ClinDatrix primarily collaborates with small to mid-sized companies but also provides specialized services to larger pharmaceutical and medical device organizations. ClinDatrix is dedicated to driving innovation and delivering high-quality support for therapeutic advancements.
Role Description
This is a contract position for Clinical Research Associates (CRA) located in FL and TX. The CRA will be responsible for overseeing and conducting clinical trials, ensuring compliance with protocols, and providing support for clinical operations. Key tasks include monitoring study progress, conducting site visits, maintaining accurate documentation, and collaborating with research teams to ensure data quality and regulatory adherence.
Qualifications
ClinDatrix, Inc. is a privately held, full-service contract research organization (CRO) founded in 2002 to support drug and medical device innovators in navigating the development and regulatory approval processes. The company offers expertise from preclinical development to regulatory filings and post-marketing studies. ClinDatrix primarily collaborates with small to mid-sized companies but also provides specialized services to larger pharmaceutical and medical device organizations. ClinDatrix is dedicated to driving innovation and delivering high-quality support for therapeutic advancements.
Role Description
This is a contract position for Clinical Research Associates (CRA) located in FL and TX. The CRA will be responsible for overseeing and conducting clinical trials, ensuring compliance with protocols, and providing support for clinical operations. Key tasks include monitoring study progress, conducting site visits, maintaining accurate documentation, and collaborating with research teams to ensure data quality and regulatory adherence.
Qualifications
- Knowledge and application of clinical trial protocols and clinical research methodologies
- Five years experience working as a Clinical Research Associate
- Familiarity with clinical operations and research practices, current ICH/GCP certification
- Excellent organizational, communication, and time-management skills
- Ability to collaborate effectively with team members
- Previous experience in Ophthalmology clinical research required