Senior Clinical Research Associate at Syngene
| Job Title | Senior Clinical Research Associate |
|---|---|
| Company | Syngene International Ltd. |
| Location | Bangalore |
| Experience | 3 – 9 years |
| Salary | 7 – 9 Lacs per annum |
| Education | M.Sc., M.Pharm, Pharm D, BAMS, BDS, MDS, BHMS, Life Sciences |
| Key Responsibilities | Site management, protocol training, quality assurance, documentation |
| Job Highlights | Work/Life Balance, Flexibility, Problem Solving |
| Application | Apply online (link provided on job listing) |
| Verified Job | Yes |
Senior Clinical Research Associate Role at Syngene International Ltd.
Syngene International Ltd., founded in 1993, is a global player in providing integrated scientific services across industries such as pharmaceuticals, biotechnology, and animal health. With clients that include major industry leaders like Bristol-Myers Squibb, GSK, Merck, and Amgen, Syngene is known for helping accelerate R&D productivity and reduce innovation costs. The company’s focus on excellence and collaboration with its clients has made it a trusted partner in scientific research worldwide. Senior Clinical Research Associate at Syngene
They are currently seeking a Senior Clinical Research Associate (CRA) to join their team in Bangalore. If you have between 3 and 9 years of relevant experience and are passionate about clinical research, this could be the perfect role for you. Senior Clinical Research Associate at Syngene
Key Responsibilities of a Senior Clinical Research Associate
As a Senior Clinical Research Associate, you will play a key role in ensuring the success of clinical trials by managing and monitoring site activities. Here’s a closer look at your responsibilities: Senior Clinical Research Associate at Syngene
Site Management and Monitoring
You will be responsible for conducting site selection, initiation, monitoring, and close-out visits. You will ensure that all activities comply with study protocols, standard operating procedures (SOPs), Good Clinical Practice (GCP), and regulatory guidelines. Senior Clinical Research Associate at Syngene
Protocol Training and Communication
One of your core responsibilities will be administering protocol and study-related training to the site staff. You will also ensure that all project expectations are clearly communicated to the research team.
Compliance and Quality Assurance
Maintaining quality and integrity throughout the study is crucial. You will monitor compliance and resolve issues in collaboration with the Clinical Project Manager (CPM) to ensure everything runs smoothly.
Performance Tracking
You will track the progress of the study site by monitoring subject recruitment, Ethics Committee submissions, CRF (Case Report Form) completion, and resolving data queries to ensure timely study completion.
Documentation and Reporting
You’ll create detailed visit reports and follow-up letters that document the activities and findings during site visits. This role requires meticulous attention to detail to ensure everything is properly documented.
Support for Project Management
In this role, you’ll assist the CPM by helping design study tools, documents, and processes that will streamline the clinical research process. You may also be required to take on a leadership role when necessary, coordinating tasks and responsibilities with the CPM and the wider project team. Senior Clinical Research Associate at Syngene
Timesheet Management
You’ll also need to ensure the timely submission of timesheets for assigned projects and tasks to ensure smooth project operations.
Educational Qualifications and Experience
To be considered for this role, you must hold one of the following degrees:
- M.Sc., M.Pharm, Pharm D
- BAMS, BDS, MDS, BHMS
- Or any other relevant life sciences degree
You will need 3 to 9 years of relevant experience in clinical research, with a strong foundation in clinical trial management and monitoring.
What You’ll Bring to the Team
Successful candidates will possess the following skills:
- Strong communication and teamwork skills, with the ability to work effectively across departments and with site staff.
- A creative and problem-solving mindset, able to think on your feet and adapt to dynamic environments.
- The ability to manage tight deadlines without compromising on quality.
- A focused and organized work ethic that ensures all tasks are completed in a timely manner.
Why Join Syngene?
By joining Syngene International Ltd., you’ll become part of an innovative and fast-growing company that values collaboration, excellence, and commitment to advancing research. You’ll work in a flexible environment that prioritizes work-life balance while giving you opportunities to grow professionally and contribute to cutting-edge research in global pharmaceuticals and biotechnology.
If you’re passionate about making an impact in clinical research, don’t miss this opportunity to be part of a dynamic and forward-thinking team at Syngene International Ltd. Senior Clinical Research Associate at Syngene
How to Apply
If you meet the qualifications and are eager to join a world-class clinical research team, submit your application online via the job listing. This position offers competitive compensation between 7 and 9 Lacs per annum.
Take the next step in your career and contribute to groundbreaking scientific research that can improve healthcare outcomes globally!
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