Clinical Trials Assistant

3 days ago

Singapore IQVIA Full time

**Responsibilities**:

- Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF)) that track site compliance and performance within project timelines.
- Assist the clinical team with the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures.
- Assist with periodic review of study files for completeness.
- Assist CRAs and RSU with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information.
- Assist with the tracking and management of Case Report Forms (CRFs), queries and clinical data flow.
- Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation.
- May accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training. Essential Functions
- Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF)) that track site compliance and performance within project timelines.
- Assist the clinical team with the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures.
- Assist with periodic review of study files for completeness.
- Assist CRAs and RSU with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information.
- Assist with the tracking and management of Case Report Forms (CRFs), queries and clinical data flow.
- Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation.
- May accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training.

**Job Requirements**:

- Bachelors Degree in Pharmaceutical or related field
- Min. 1 - 3 years of experience in clinical research environment
- Basic knowledge of applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
- Broad knowledge of applicable protocol requirements as provided in company training
- Computer skills including working knowledge of Microsoft Word, Excel and PowerPoint
- Good written and verbal communication skills including good command of English language
- Effective time management and organizational skills
- Ability to establish and maintain effective working relationships with coworkers, managers and clients

  • Clinical Trial Specialist

    3 days ago

    Singapore Emerald Clinical Full time

    Overview At Emerald Clinical Trials , we are a global, full-service Contract Research Organization (CRO) with a rich heritage in the Asia-Pacific region. We are dedicated to advancing clinical research through scientific expertise and operational excellence, supporting biopharmaceutical, medical device, and diagnostic customers across all trial phases,...

  • Clinical Trial Specialist

    6 days ago

    Singapore Emerald Clinical Full time

    Join to apply for the Clinical Trial Specialist role at Emerald Clinical At Emerald Clinical Trials , we are a global, full-service Contract Research Organization (CRO) with a rich heritage in the Asia-Pacific region. We are dedicated to advancing clinical research through scientific expertise and operational excellence, supporting biopharmaceutical,...

  • Clinical Trial Specialist

    3 days ago

    Singapore Emerald Clinical Full time

    Join to apply for the Clinical Trial Specialist role at Emerald Clinical At Emerald Clinical Trials , we are a global, full-service Contract Research Organization (CRO) with a rich heritage in the Asia-Pacific region. We are dedicated to advancing clinical research through scientific expertise and operational excellence, supporting biopharmaceutical,...

  • Clinical Trial Specialist

    6 days ago

    Singapore Emerald Clinical Full time

    Overview At Emerald Clinical Trials , we are a global, full-service Contract Research Organization (CRO) with a rich heritage in the Asia-Pacific region. We are dedicated to advancing clinical research through scientific expertise and operational excellence, supporting biopharmaceutical, medical device, and diagnostic customers across all trial phases, from...

  • Clinical Trial Assistant

    6 days ago

    Singapore Medpace Full time

    Clinical Trial Assistant (Site Contracts) Join to apply for the Clinical Trial Assistant (Site Contracts) role at Medpace Clinical Trial Assistant (Site Contracts) Join to apply for the Clinical Trial Assistant (Site Contracts) role at Medpace Our global activities are growing rapidly, and we are currently seeking a full-time, office-based Clinical Trial...

  • Clinical Trials Assistant

    1 week ago

    Singapore IQVIA Full time

    **Responsibilities**: - Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF)) that track site compliance and performance within project timelines. - Assist the clinical team with the preparation, handling, distribution, filing,...

  • Clinical Trials Assistant

    2 weeks ago

    Singapore IQVIA Full time

    **Responsibilities**: - Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF)) that track site compliance and performance within project timelines. - Assist the clinical team with the preparation, handling, distribution, filing,...

  • Clinical Trials Assistant

    1 week ago

    Singapore IQVIA Full time

    **Responsibilities**: - Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF)) that track site compliance and performance within project timelines. - Assist the clinical team with the preparation, handling, distribution, filing,...

  • Fsp Clinical Operations Specialist

    5 days ago

    Singapore Syneos Health Clinical Full time

    **FSP Clinical Operations Specialist / Clinical Trial Assistant** **-** **(** **22007296** **)** **Description** **Clinical Operations Specialist** Come discover what our 25,000+ employees already know: work here matters everywhere. We’re a growing and evolving biopharmaceutical industry leader, which means you’ll have endless opportunities to work...

  • Clinical Trial Assistant

    3 days ago

    Singapore SYNEOS HEALTH SINGAPORE PTE. LTD. Full time

    The position is responsible for providing clerical, administrative, and technical administrative support to one or more business units or clients within Clinical Operations. - Responsible for performing activities in compliance with applicable Corporate and Clinical Operations Policies, Standard Operating Procedures and Work Instructions - Assists Clinical...