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Syngene
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Senior Clinical Research Associate

Senior Clinical Research Associate

Syngene

3 - 9 years

6 - 7 Lacs

kolkata mumbai new delhi hyderabad pune chennai bengaluru

Posted:2 days ago| Platform:

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Skills Required

ehs site management quality standards gcp site selection senior clinical research associate clinical research associate operations monitoring recruitment

Work Mode

Work from Office

Job Type

Full Time

Job Description

Overall adherence to safe practices and procedures of oneself and the teams aligned
Contributing to development of procedures, practices and systems that ensures safe operations and compliance to company s integrity & quality standards
Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace at all times.
Ensuring safety of self, teams and lab/plant by adhering to safety protocols and following environment, health, and safety (EHS) requirements at all times in the workplace.
Ensure all assigned mandatory trainings related to data integrity, health, and safety measures are completed on time by all members of the team including self
Compliance to Syngene s quality standards at all times
Hold self and their teams accountable for the achievement of safety goals
Govern and Review safety metrics from time to time

Core Purpose of the Role :

Perform site selection, initiation, monitoring and close-out visits in accordance with contracted scope of work, Standard Operating Procedures and all the applicable Good Clinical Practice (GCP) Guidelines and Regulations.
Responsible for site management for the assigned protocols, sites and therapeutic areas
Complete appropriate Standard Operating procedure training, therapeutic area training, protocol training and any relevant training required to perform job duties
Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectation and activities
Ensure the quality and integrity of study conducted at site level in accordance with protocol and applicable regulations. Investigate and discuss quality issues with Clinical Project Manager for resolution and implementation of Corrective Action and Preventive Action
Manage the progress and performance of the assigned study sites by following activities but not limited to: tracking regulatory and Ethics Committee submissions and approvals, subject recruitment, case report form (CRF) completion and submission, and data query generation and resolution.

Role Accountabilities

Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentations.
Timely submission of timesheets for Project specific and other tasks.

Leadership Capabilities

Provide assistance to the Clinical Project Manager with design of study tools, documents and processes.
Assignment as a Lead Clinical Research Associate (if required), the responsibilities could include:

Supporting the Clinical Project Manager for coordination with-in the project team.
Delegation of project level Clinical Project Manager responsibilities
The above responsibilities would be assigned by reporting manager and project-level task allocation would be performed.

Syngene Values

All employees will consistently demonstrate alignment with our core values

Excellence
Integrity
Professionalism

Specific requirements for this role

Experience
Demonstrated Capability
Education

Experience

3 - 9 Years

Skills and Capabilities

Should have good communication skill and should be a good team player.
Ability to work successfully in a dynamic, ambiguous environment.
Ability to meet tight deadlines and prioritize workloads.
Ability to develop new ideas and creative solutions.
Should be a focused employee.

Education

M. Sc/M. Pharm/Pharm D, BAMS, BDS, MDS & BHMS/Any life science

Equal Opportunity Employer

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