Pharma Job Opportunity in Clinical Research Jobs | ThermoFischer hiring Clinical Trial Coordinator Role | Apply Now
Searching for a rewarding Pharma Job in the clinical industry? This excellent opportunity in Clinical Research Jobs is ideal for Pharmacy graduates looking to build a successful career in clinical trials and global pharmaceutical innovation. Candidates will gain valuable exposure to international studies, clinical systems, and project coordination while working in a fast-growing research environment.
- Job Title: Clinical Trial Coordinator
- Location: India
About the Company
Thermo Fisher Scientific is a global leader in scientific research services, laboratory solutions, pharmaceuticals, and biotechnology innovation. The company supports pharmaceutical and biotech organizations worldwide through advanced clinical research, laboratory technologies, and healthcare solutions. With operations across more than 100 countries, Thermo Fisher Scientific plays a major role in accelerating drug development, clinical trials, and scientific discoveries that improve global health.
Key Responsibilities
- Coordinate and manage assigned clinical trial activities.
- Review study and investigator documents and update records in the system.
- Ensure tasks are completed on time, within budget, and with high quality.
- Maintain study documentation, trackers, training records, and eTMF systems.
- Provide support for clinical systems like CTMS and eTMF.
- Handle administrative tasks, reports, and trial-related communications.
- Organize meetings and prepare meeting minutes.
- Analyze study reports and resolve documentation issues.
- Maintain vendor trackers and support site material distribution.
- Assist in managing Investigator Site Files (ISF) and pharmacy study supplies.
Qualification
- Bachelor’s/Master’s degree in Pharmacy
- Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 1-2 years).
Knowledge, Skills, and Abilities
- Ability to work independently and as part of a team.
- Strong organizational and multitasking skills with attention to detail.
- Ability to analyze data and maintain accuracy in clinical systems.
- Good communication and customer-focused approach.
- Flexible and adaptable to changing project timelines.
- Knowledge of clinical research regulations, ICH-GCP guidelines, and SOPs.
- Excellent English communication and presentation skills.
- Proficiency in MS Office tools like Word, Excel, and PowerPoint.
- Ability to learn and manage clinical trial database systems.
- Self-motivated with a positive attitude and strong interpersonal skills.
- Capability to complete clinical training programs successfully.
