Associate Director, Clinical Research Associate Manager

Ind - Maharashtra - Mumbai (wework)executive

HealthcareClinical Researcher

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Quick Summary

Key Responsibilities

• Work allocation, staff development and performance appraisal. • Provides input for capacity planning, including reporting of current manpower and forecasting of CRA capacity and needs,

Requirements Summary

Masters in science, Master's in Pharmacology/.Pharmacy/ Clinical Research CORE Competency Expectations: • Ability to work independently and in a team environment• Excellent people management,

Technical Tools

HealthcareClinical Researcher

Job Description

This role will be key to ensure strong monitoring in our clinical trials. Under the oversight of the CRD or Head of Site Management and Monitoring, the person is responsible to manage a team of 6-14 CRAs and to ensure excellent study and site performance with strict adherence to local regulations, company SOPs and ICH GCP.

As line manager the role is critical to continuously develop key talents by providing training, support and mentoring to the CRAs and properly manage situation of low or non-performance.

The role will work at country level with other local stakeholder e.g. CRM to ensure alignment and development of the country capabilities. The role will collaborate with country PLMs to ensure alignment across all monitoring functions. The person contributes to HQ capacity/resource planning activities to ensure efficient allocation of resources and work.

Responsibilities

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o Manage CRA – career development, performance reviews, etc., including addressing low-performance situations, and taking appropriate actions.

o Support and resolve escalation of issues from CRAs.

o Liaise with local HR and finance functions as required.

o Contribute to HQ capacity/resource planning activities to ensure efficient allocation of resources and work. Manage local conflicts between resource and work.

o Provides training, support and mentoring to the CRA to ensure continuous development.

o Ensures CRA compliance to corporate policies, procedures and quality standards

Requirements

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What We Offer

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Adaptability, Adaptability, Career Planning, Clinical Research, Clinical Research Management, Clinical Trial Documentation, Clinical Trial Management, Clinical Trial Planning, Clinical Trials Monitoring, Clinical Trials Operations, Cross-Cultural Awareness, Decision Making, Ethical Standards, Global Coordination, Good Clinical Practice (GCP), Liaison Work, Line Management, Oncology Trials, On Site Management, People Leadership, Performance Feedback, Policy Compliance, Procedure Adherence, Process Alignment, Process Standardization {+ 7 more}