Opportunity to work as a Home Base CRA / CTA / CRC @ Lambda Therapeutic Research Ltd.
Job Description
CRA Job Description
Perform site identification and conduct feasibility studies
Perform site selection visit, site initiation visit in accordance with the protocol and other applicable regulatory guidelines including local regulatory guidelines.
Perform site monitoring visit and site close-out visit in accordance with the protocol and other applicable regulatory guidelines including local regulatory guidelines.
Send follow up letter to sites and submit visit reports to the clinical team leader / Project manager as required.
Keep a close association with site(s) for patient recruitment, patient follow up and protocol related activities.
Act as a communication link between sponsor and the site
Maintain accurate and timely sponsor / site correspondence and communication.
Attend investigators meeting
Training of investigators on protocol and other applicable regulatory guidelines including local regulatory guidelines.
Prepare Ethics Committee submission packages.
Help in preparation of regulatory binder.
Maintain updated sites files and collection of the essential documents and project related documents during the site visits and maintain central clinical file.
CRF retrieval as per project instructions.
Coordinate and distribute clinical study material to study sites.
Archival of study documents.
BABE Monitoring
website : www.lambda-cro.com
Salary: INR 2,00,000 - 5,00,000 P.A
Industry: Pharma / Biotech / Clinical Research
Functional Area: Medical, Healthcare, R&D, Pharmaceuticals, Biotechnology
Role Category: Clinical Research Associate/Scientist
Role: Clinical Research Associate/Scientist
Keyskills: CRA, Clinical Trial, Home Base CRA, Clinical Research, site monitoring
Desired Profile
Education:UG -Any Graduate - Any Specialization, Graduation Not Required
PG - Any Postgraduate - Any Specialization, Post Graduation Not Required
Doctorate - Any Doctorate - Any Specialization, Doctorate Not Required
Company Profile
Lambda Therapeutic Research Limited is a leading global Clinical Research Organization (CRO) headquartered in Ahmedabad - India, with facilities and operations in Mumbai (India), Toronto (Canada), Warsaw (Poland), London (UK) and USA. Lambda offers full spectrum clinical trial solutions empowered by more than 14 years of service to the biopharmaceutical and generic industry. At Lambda, our comprehensive services are executed with comprehensive efforts, to deliver positive results. Led by a management team of highly qualified & experienced industry leaders, we apply innovative technologies, therapeutic expertise and a commitment to quality in order to help clients develop products safely, effectively and quickly. Website : www.lambda-cro.com
Click here to apply
Job Description
CRA Job Description
Perform site identification and conduct feasibility studies
Perform site selection visit, site initiation visit in accordance with the protocol and other applicable regulatory guidelines including local regulatory guidelines.
Perform site monitoring visit and site close-out visit in accordance with the protocol and other applicable regulatory guidelines including local regulatory guidelines.
Send follow up letter to sites and submit visit reports to the clinical team leader / Project manager as required.
Keep a close association with site(s) for patient recruitment, patient follow up and protocol related activities.
Act as a communication link between sponsor and the site
Maintain accurate and timely sponsor / site correspondence and communication.
Attend investigators meeting
Training of investigators on protocol and other applicable regulatory guidelines including local regulatory guidelines.
Prepare Ethics Committee submission packages.
Help in preparation of regulatory binder.
Maintain updated sites files and collection of the essential documents and project related documents during the site visits and maintain central clinical file.
CRF retrieval as per project instructions.
Coordinate and distribute clinical study material to study sites.
Archival of study documents.
BABE Monitoring
website : www.lambda-cro.com
Salary: INR 2,00,000 - 5,00,000 P.A
Industry: Pharma / Biotech / Clinical Research
Functional Area: Medical, Healthcare, R&D, Pharmaceuticals, Biotechnology
Role Category: Clinical Research Associate/Scientist
Role: Clinical Research Associate/Scientist
Keyskills: CRA, Clinical Trial, Home Base CRA, Clinical Research, site monitoring
Desired Profile
Education:UG -Any Graduate - Any Specialization, Graduation Not Required
PG - Any Postgraduate - Any Specialization, Post Graduation Not Required
Doctorate - Any Doctorate - Any Specialization, Doctorate Not Required
Company Profile
Lambda Therapeutic Research Limited is a leading global Clinical Research Organization (CRO) headquartered in Ahmedabad - India, with facilities and operations in Mumbai (India), Toronto (Canada), Warsaw (Poland), London (UK) and USA. Lambda offers full spectrum clinical trial solutions empowered by more than 14 years of service to the biopharmaceutical and generic industry. At Lambda, our comprehensive services are executed with comprehensive efforts, to deliver positive results. Led by a management team of highly qualified & experienced industry leaders, we apply innovative technologies, therapeutic expertise and a commitment to quality in order to help clients develop products safely, effectively and quickly. Website : www.lambda-cro.com
Click here to apply
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