Clinical Research Associate

Essential Qualification:

• Bachelors or Masters in Pharmacy-Pharmacology-Pharmaceutics
• Diploma in Clinical Research
• Bachelors or Masters in Homeopathy
• MBBS with Experience in Clinical Research & Trials, Site Monitoring & Research

Preferable: Good analytical skills with research and publishing mindset, knowledge of statistical data analysis, Microsoft Excel & SPSS, Good communication & written skill in English & soft skills. Experience: 1-5 Years Location: Durgapur, West Bengal

Job Description (JD)

Responsibilities:

• Obtain screening consent from the volunteer, Recording of Demographics, Filing of habit questionnaires,
• Recording details of screening and maintaining screening log,
• Receive volunteer age proof, address proof & photograph,
• Allotting volunteers database number and maintaining the same,
• Checking volunteer enrolment form and enrolment questionnaire,
• Registration and monitoring of volunteers / study participants
• Maintaining study flow,
• Recording and maintaining study logs,
• Ensuring the CRF and related documents are complete,
• Storage of protocols, files related to Clinical Trials, Thesis & Ethics Committee (EC),
• Facing internal & external audits related to clinical trials, EC,
• Coordination between principal investigator, sponsor, EC & other Stakeholders,
• Maintain required regulatory submissions,
• Screening patents and dispense drugs, ensure timely follow up visits, detect possible adverse events, regular patient monitoring, data analysis, data entry for Clinical Studies & research studies.
• Assist Principal Investigator (PI) & DNB students in research, protocol writing, publishing.
• Experience in medical writing & publication.