Clinical Research Operations Support at SGS

Muntinlupa, Metro Manila, Philippines -

Full Time

Start Date

Immediate

Expiry Date

29 Jul, 26

Salary

0.0

Posted On

30 Apr, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Trials, Document Management, Regulatory Compliance, Project Management, Data Quality, SOP Development, Communication, Customer Service, TMF Management, ISF Management, Regulatory Affairs, Quality Assurance, Time Management, Multi-tasking, Operational Excellence

Industry

Professional Services

Description

Company Description We are SGS – the world’s leading testing, inspection and certification company. We are recognized as the global benchmark for quality and integrity. Our 93,000 employees operate a network of 2,600 offices and laboratories, working together to enable a better, safer and more interconnected world. Job Description Primary Responsibilities As a member of the team in our Global Business Solutions (GBS) center, responsible for managing and reviewing and filing study documents that are used on clinical trials. This position is also responsible for written and verbal correspondence with the internal team as well as regulatory authorities, ethics committees, investigators, monitors, and sponsors. Specific Responsibilities At all times, complies with SGS Code of Integrity and Professional Conduct. Responsible for maintaining the filing system and managing the central study documentation (TMF/ISF) Assists in the development of study documents and study submission. Assists with written and verbal correspondence with regulatory authorities, ethics committees, investigators, monitors, and sponsors Assists in the reviewof study documents. Assist with the development and updating of SOPs, Work Instructions, and training material related to study paperwork creation. Supports collaboration with external service providers (e.g., hospitals, laboratories) Ensure compliance with regulations. Provides excellent customer service to clients and maintains positive interaction with peers and supervisors. Adheres to internal standards, policies, and procedures. Performs other duties as assigned by the project manager or team lead. Performs other related duties as may be assigned either in support of departmental goals or for his/her personal or professional training, education or development as programmed by his/her immediate superior. Ensures work area in GBS is kept clean and presentable at all times. Remains familiar with SGS quality assurance procedures. Complies to all SGS health and safety and HR policies and procedures. Qualifications Minimum Bachelor of Science degree or equivalent technical or professional qualification. Minimum of 1 year’s prior experience in a related field or project management preferred. Ability to coordinate multiple projects at once. Ability to work independently, use time wisely and multi-task. Demonstrated commitment to data quality and operational excellence.

Responsibilities

The role involves managing and filing clinical trial study documentation while maintaining correspondence with regulatory authorities, ethics committees, and investigators. Additionally, the position supports the development of SOPs and ensures compliance with internal standards and quality assurance procedures.