Icon Plc Hiring Clinical Trial Assistant in Bangalore
- Job Overview
- Key Responsibilities
- Required Skills and Qualifications
- Benefits of Working at Icon Plc
- How to Apply
Icon Plc Hiring Clinical Trial Assistant in Bangalore: Join ICON Team
Icon Plc, a world-leading healthcare intelligence and clinical research organization, is hiring a Clinical Trial Assistant in bangalore. If you have a degree in Life Science and experience clinical research experience, this could be the perfect opportunity for you.
Job Overview
Position: Clinical Trial Assistant
Location: Icon Plc, bangalore
Qualification: Degree in Life Science preferred
Application Deadline: Open until filled
Icon Plc is at the forefront of clinical research, providing outsourced services to pharmaceutical, biotechnology, medical device, and government organizations. As a Clinical Trial Assistant, you will play a crucial role in supporting the Clinical Trial Management and Project Management teams with operational activities, ensuring the success of our clinical trials.
Key Responsibilities
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- Keeping up to date with all the changes/required knowledge on ICH GCP.
- May be responsible for supporting multiple studies simultaneously and must prioritize appropriately to meet business needs to ensure delivery of results.
- Maintain all the study trackers and access
- Analysis of various reports
- Timely distribution of dashboards and reports to the study team
- Maintain all the study trackers and access
- Analysis of various reports
- Timely distribution of dashboards and reports to the study team
- Common email group to support the issues related to CSAP, CTMS
- Clinical admin support
- Support to studies where there is no requirement of SDS
- Work closely with SDS/SM to manage the activities post SAC and till final archival.
- Managing study systems
- TMF Management and Maintenance
- Managing TMF activities both for Inhouse and FSO trials • Provide timely follow up with the stakeholders to improve the TMF compliance
Required Skills and Qualifications
- Excellent technical/IT skills. Able to understand the impact of technology on studies and to use and develop computer skills.
- Knowledge of ICH GCP relevant operational procedures, systems, and quality guidelines regarding clinical studies
- Able to work independently as well as in a team.
- Professional attitude with good customer focus (internal and external)
- Time Management as system updates, eTMF etc. need to be done in a timely manner.
- Very good communication skills
- 1-2 years of prior experience in clinical operations
Benefits of Working at Icon Plc
At Icon Plc, our people are our greatest strength. We offer a comprehensive and competitive total reward package that includes:
- Competitive Pay: Excellent base pay with a wide range of variable pay and recognition programs.
- Employee Benefits: Best-in-class employee benefits tailored to support you and your family at all stages of your career.
- Supportive Policies: Policies and initiatives designed to ensure a workplace free of discrimination and harassment.
- Professional Development: Continuous learning culture with engaging work and opportunities for professional growth.
Icon Plc is an equal opportunity and inclusive employer. We are committed to providing a workplace free of discrimination and harassment, and all qualified applicants will receive equal consideration for employment.
How to Apply
Interested candidates should prepare a comprehensive resume detailing their educational background and relevant experience. To apply, visit Icon Plc Careers page.
Application Deadline: Open until filled
To apply for this job please visit careers.iconplc.com.