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    Senior CRA Career at Syngene – MPharma Apply Now

    Syngene Careers: Senior CRA Opportunity | Pharma Jobs in Bangalore | Apply Now

    Syngene Careers presents an excellent opportunity for professionals seeking Pharma Jobs in Bangalore, with an opening for a Senior Clinical Research Associate (Senior CRA). This role in Clinical Operations focuses on site management, clinical monitoring, GCP compliance, and leadership support within an innovation-led CRO environment at Syngene.

    Job Details

    • Job Title: Senior CRA
    • Department: Clinical Operations
    • Job Location: Bangalore

    About the Company

    Syngene is an innovation-led contract research, development, and manufacturing organization offering integrated scientific services from early discovery to commercial supply, providing Pharma Jobs in Bangalore.
    At Syngene, safety is at the heart of everything we do personally and professionally. Syngene has prioritized safety alongside business performance, with a shared responsibility and accountability approach. This includes adhering to safety guidelines, procedures, and SOPs in letter and spirit.

    Job Description

    • Perform site selection, initiation, monitoring, and close-out visits in accordance with the 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 expectations and activities.
    • Ensure the quality and integrity of studies conducted at the site level in accordance with protocol and applicable regulations.

    Safety & Compliance Responsibilities 

    • Overall adherence to safe practices and procedures for self and teams
    • Contribute to the development of procedures ensuring safe operations and compliance
    • Drive an EHS mindset at the workplace
    • Ensure completion of mandatory data integrity, health, and safety trainings
    • Compliance with Syngene’s quality standards at all times
    • Govern and review safety metrics periodically

    Leadership Capabilities

    • Assist the Clinical Project Manager with the design of study tools and processes
    • Assignment as Lead Clinical Research Associate (if required)
    • Support the Clinical Project Manager in project coordination
    • Delegate project-level Clinical Project Manager responsibilities as assigned

    Qualifications

    • Education:  M.Pharm / Pharm D
    • Experience: 3 – 9 Years

    Skills and Capabilities

    • Good communication skills and a team-player mindset
    • Ability to work in a dynamic and ambiguous environment
    • Ability to meet tight deadlines and prioritize workloads
    • Ability to develop new ideas and creative solutions
    • Focused and disciplined work approach

    Equal Opportunity Employer

    Syngene provides equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, disability, race, religion, gender, sexual orientation, gender identity, genetic information, marital status, veteran status, or any other characteristic protected by applicable legislation or local law.

    CLICK HERE TO APPLY ONLINE

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