CRA II

Syngene; Electronic City; On-site; INR 600,000 - 900,000; Full time

Job summary

Syngene is seeking a CRA II for Bangalore to oversee site management and monitoring activities in accordance with GCP and contracted scope. You will train sites, ensure protocol adherence, manage data queries, and coordinate with Clinical Operations teams to ensure timely delivery of study milestones.

The role requires strong communication, the ability to work in a dynamic environment, and a focus on safety and quality in clinical trials.

Qualifications

• Experience as Clinical Research Associate II.
• Proficiency in communicating with sites and teams.
• Ability to adapt in a dynamic, ambiguous environment.
• Capability to meet tight deadlines and prioritize tasks.
• Strong focus and problem-solving mindset.

Responsibilities

• Perform site selection, initiation, monitoring and close-out visits per SOPs and GCP.
• Manage assigned protocols, sites and therapeutic areas with regular communication.
• Ensure data integrity and query resolution with CRP guidance.
• Track regulatory submissions, ethics approvals and site performance.

Skills

communication

team player

deadline management

creative thinking

focus and concentration

Education

MSc in life sciences

M.Pharm/PharmD

BAMS/BDS/MDS/BHMS

other life sciences

Job description

JOB DESCRIPTION

Job Title: CRA II

Job Location: Bangalore

Department: CLINICAL OPERATIONS T&CR

About Syngene: Syngene (www.syngeneintl.com) is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply.

At Syngene, safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures and SOPs, in letter and spirit

Mandatory expectation for all roles as per Syngene safety guidelines

• 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 companys 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.

Syngene Values

All employees will consistently demonstrate alignment with our core values

• Excellence
• Integrity
• Professionalism

Experience

Looking for candidate with experience as a Clinical Research Associate II

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

It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. In addition, Syngene will provide reasonable accommodations for qualified individuals with disabilities.