Dental Job at Syngene in Bangalore | Apply Now
If you are looking for dental jobs in Bangalore beyond traditional clinical practice, this opportunity at Syngene International Limited could be a great career move. This dental job in Clinical Operations offers dentists the chance to work in clinical research and contribute to innovative drug development while building a rewarding career in the pharmaceutical industry.
Job Details:
- Job Position: CTA-ClinOps
- Location: Bangalore, India
- Department: Clinical Operations – T&CR
About the Company:
Syngene International Limited is a leading innovation-driven contract research, development, and manufacturing organization (CRDMO) headquartered in Bangalore, India. Established in 1993, the company provides integrated scientific services that support the entire drug discovery and development lifecycle – from early discovery research to clinical development and commercial manufacturing.
Syngene partners with global pharmaceutical, biotechnology, and healthcare companies to accelerate scientific innovation and bring new therapies to patients worldwide. The organization offers expertise in areas such as drug discovery, clinical development, biologics, small molecules, and specialty chemical development.
Job Description:
This dental job in Clinical Operations focuses on supporting clinical trial activities and documentation management. The position involves assisting Clinical Study Managers (CSM) and Clinical Research Associates (CRA) by accurately updating and maintaining clinical systems that track site compliance and performance within project timelines.
Qualifications:
- Education: BDS, MDS
- Experience: Candidates with experience as a Clinical Research Coordinator (CRC) or other relevant experience in core clinical trial conduct are preferred.
Skills and Capabilities:
- Good communication skills and ability to work effectively in teams
- Ability to work in a dynamic and ambiguous environment
- Ability to meet tight deadlines and prioritize workloads
- Capability to develop new ideas and creative solutions
- Strong focus and attention to detail
Key Responsibilities:
Document Management
- Maintain and update the Trial Master File (TMF) and/or Investigator Site Files (ISF)
- Ensure proper filing, tracking, and archiving of clinical documents such as protocols, informed consent forms, and approvals
- Perform quality checks on trial documents for completeness and accuracy
- Support the team in timely regulatory and ethics committee submissions and maintain records
Regulatory Support
- Assist in preparation and submission of documents to regulatory authorities and ethics committees
- Track regulatory approvals and study start-up milestones
Clinical Trial Coordination
- Support CRA and CSM teams in planning and tracking clinical trial activities
- Assist in scheduling investigator meetings, site initiation visits, monitoring visits, and close-out visits
Communication & Liaison
- Act as a communication hub between internal teams (CRAs, CSM, and cross-functional teams such as data managers) and external stakeholders such as study sites and vendors
- Distribute study-related communications and updates to sites and team members
Data Entry & Tracking
- Support leadership and CSM teams in maintaining study status reports including data entry tracking, protocol deviations and document filing
- Enter and track data in clinical trial management systems (CTMS)
- Maintain logs including site contact lists, screening/enrollment logs, and essential document trackers
Trial Supply Management
- Support CRA and CSM teams in coordinating shipment of study supplies and investigational products (IP) to sites and maintaining documentation
- Track inventory and reconcile supplies with site reports
Audit & Inspection Support
- Prepare documentation for internal or regulatory audits and inspections
- Assist in responding to audit findings or follow-up actions
Training & Compliance
- Maintain training records for site and sponsor personnel
- Ensure adherence to Good Clinical Practice (GCP), standard operating procedures (SOPs), and regulatory requirements
