Clinical Trial Coordinator Jobs

Key Responsibilities:1. Trial Architecture:> Contribute to the development of dynamic trial plans and protocols in tandem with the clinical operations team.> Collaborate on the strategic selection and qualification of investigative sites.2. Site Symphony:> Conduct harmonious site initiation, monitoring, and close-out visits to ensure seamless protocol execution and pristine data collection.> Cultivate collaborative relationships with investigative site teams, providing support and guidance.3. Regulatory Mastery:> Ensure meticulous adherence to regulatory standards, guidelines, and the principles of Good Clinical Practice (GCP).> Spearhead the preparation and submission of regulatory documents to ethics committees and regulatory authorities.4. Data Choreography:> Direct the orchestration of data collection, ensuring the accuracy and completeness of clinical trial data.> Collaborate with data management teams to resolve data discrepancies and maintain a symphony of data quality.5. Risk Ballet:> Proactively identify potential risks to trial success and choreograph mitigation strategies in collaboration with project teams.6. Communication Sonata:> Cultivate clear and resonant communication channels with internal and external stakeholders.> Compose eloquent and timely study progress reports, fostering transparency and accountability.Qualifications:Bachelor's or advanced degree in a relevant field (Life Sciences, Nursing, etc.).Demonstrated experience as a Clinical Research Associate, preferably in the pharmaceutical or biotechnology domain.Profound knowledge of clinical trial processes, regulatory requirements, and GCP.Exceptional interpersonal and communication finesse

Position: Clinical Research CoordinatorQualification Bio Science (B.Pharm/Bio Tech etc.)Experience Above 1 Year (Clinical Research Experience must) Timing General ShiftSalary 2L 2.5L (Per annum)Location Visakhapatnam/Chennai/BangaloreLanguage Know English/Kannada/TeluguJOB Description Clinical Research Coordinator To have the good knowledge of regulations and GCP guidelines. Ability to communicate properly between the physician, patient & the site head. Assist Senior CRC in Screening including informed consent process, randomization, enrolment & follow-up (including Telephonic Follow-up) process & procedures. Maintenance of Investigator Master File as per Good documentation practices & SOP including generation of source documents. Present in Site Initiation Visit, Monitoring Visits, Site Closeout Visit. CRF, e-CRF entry, Data Query resolution. Coordinate between the local/Central laboratory and courier for the shipment. Assist the pharmacist in drug accountability and temperature maintaining logs. Assist the Sr. CRC in maintaining the accountability of study materials and in scheduling study procedures. Endow the required file notes, weekly and monthly and monthly report to the reporting authority. Tracking the status of all study activities. Report Sr.DGM daily and take advice for further action.