Novo Nordisk is hiring B. Pharma/ M. Pharma/ Pharma D as a Clinical Research Ass
PHARMACY INDIA, May, MO, United States
Novo Nordisk is seeking talented professionals with qualifications in B. Pharma, M. Pharma, Pharma D, MBBS, BDS, BAMS, BHMS, B. Sc, or M. Sc for the role of Clinical Research Associate in the dynamic Ahmedabad region. This exciting opportunity allows you to join a global leader in healthcare and contribute to groundbreaking clinical research. If you have a passion for medical science and a commitment to advancing patient care, Novo Nordisk invites you to apply and be part of their innovative team.
Position
Clinical Research Associate
Category
Clinical Development
Department
Clinical Medical Regulatory (CMR)
Qualifications
B. Pharma / M. Pharma / Pharma D / MBBS / BDS / BAMS / BHMS / B. Sc / M. Sc
Certified in ICH GCP trained is preferred.
Additional qualification on clinical research would be preferred.
Experience
2 – 4 years of experience as a Clinical Research Associate.
Experience in 1-2 multinational clinical trials phase 2-3 from site initiation till site closure preferred.
Responsibilities
Taking leadership of site management for the selection (if applicable) and initiation of sites as well as conduction and closing activities of the appointed studies in compliance with local regulations, ICH‑GCP, NN procedures and protocol requirements to ensure data quality and study subject protection.
Responsible for recruitment at site level, delivering results that directly impact the successful completion of the clinical programme. Coordinating with CRM and RTM and communicating progress and critical issues that may impair trial progress; may have direct contact with ITM in some cases.
Efficient and accurate site selection visits (as appropriate including analysis of site logistics, site performance/quality indicators).
Accountability for patient recruitment strategies, including implementation of mitigation actions.
Visit trial sites regularly in accordance with the protocol to perform monitoring activities required.
Proactive use of IT Systems (e.g., IMPACT, EDC) for preparation and conduct of site visits as well as source data verification in collaboration with data management/logistics team.
Location
Ahmedabad, Gujarat, IN
Job Type
Full Time
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Position
Clinical Research Associate
Category
Clinical Development
Department
Clinical Medical Regulatory (CMR)
Qualifications
B. Pharma / M. Pharma / Pharma D / MBBS / BDS / BAMS / BHMS / B. Sc / M. Sc
Certified in ICH GCP trained is preferred.
Additional qualification on clinical research would be preferred.
Experience
2 – 4 years of experience as a Clinical Research Associate.
Experience in 1-2 multinational clinical trials phase 2-3 from site initiation till site closure preferred.
Responsibilities
Taking leadership of site management for the selection (if applicable) and initiation of sites as well as conduction and closing activities of the appointed studies in compliance with local regulations, ICH‑GCP, NN procedures and protocol requirements to ensure data quality and study subject protection.
Responsible for recruitment at site level, delivering results that directly impact the successful completion of the clinical programme. Coordinating with CRM and RTM and communicating progress and critical issues that may impair trial progress; may have direct contact with ITM in some cases.
Efficient and accurate site selection visits (as appropriate including analysis of site logistics, site performance/quality indicators).
Accountability for patient recruitment strategies, including implementation of mitigation actions.
Visit trial sites regularly in accordance with the protocol to perform monitoring activities required.
Proactive use of IT Systems (e.g., IMPACT, EDC) for preparation and conduct of site visits as well as source data verification in collaboration with data management/logistics team.
Location
Ahmedabad, Gujarat, IN
Job Type
Full Time
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