Pan Gong
Changsha,Hunan,China
Summary
Accomplished Clinical Research Associate with 4 years of experience performing and documenting pre-study site evaluations, regulatory document collection, interim monitoring and study close-out visits. Diligent in performing studies aligned with good clinical practices, study-specific requirements and clinical monitoring plans. In-depth knowledge of company procedures, regulatory requirements and quality standards.
Detail-oriented Clinical Research Associate well-versed in coordinating operations, managing sites and drafting detailed clinical reports. Knowledgeable about action planning, database locking and standard operating procedures. Supports participant recruitment and management to meet research objectives. Hardworking Pianzaihuang Project (Hunan Cancer Hospital) successfully leads site evaluations, initiations and closeouts. Well-versed in research trials and of picks up new procedures quickly. Offering advanced planning, problem-solving and communication skills developed over 4 + years of clinical research success.
Overview
6
6
years of professional experience
1
1
Certification
Work History
Clinical Research Associate
Beijing Bonowi Pharmaceutical Technology Co., Ltd.
08.2023 - Current
- Involved in Study Start-Up (SSU) preparations, including communication with research centers, document preparation, and submission
- Conducted regular monitoring visits to ensure compliance with trial protocols
- Managed trial drug supplies and ensured compliance with regulations.
Clinical Research Associate
Beijing Excellent Future International Pharmaceutical Technology Co., Ltd.
02.2021 - 06.2023
- Managed over 10 clinical trial protocols and research centers, significantly improving research quality and compliance efficiency
- Maintained over 500 related documents to ensure the integrity and accuracy of research documentation.
Clinical Coordinator
Shanghai Baishida Pharmaceutical Technology Co., Ltd.
10.2018 - 02.2020
- Improved the accuracy of adverse event recording and reporting to 98%, ensuring the safety monitoring of research
- Optimized drug management processes, ensuring compliance and safety.
Education
Bachelor of Science - Nursing
Hunan University of Chinese Medicine
Changsha,Hunan07.2015
Skills
- Clinical Research Expertise: Well-versed in clinical trial processes, including trial design, data collection, monitoring, and reporting Proficient in using Electronic Data Capture (EDC) systems for data entry, verification, and quality control
- Medical Ethics Knowledge: Comprehensive understanding of medical ethics, ensuring the protection of participant rights in clinical trials
- Communication and Coordination: Strong communication and coordination skills, effectively liaising with research teams, medical institutions, and regulatory bodies
- Site Management
- Detailed documentation
Accomplishments
Inferior Vena Cava Filter Project (Hunan Provincial People's Hospital)
·February 2021 - November 2022
Chaihuang Lidan Capsules Project (The First Affiliated Hospital of Hunan University of Chinese Medicine)
February 2021 - December 2021
Pianzaihuang Project (Hunan Cancer Hospital)
October 2021 - June 2023
Ginkgo Biloba Dropping Pills Project (Changsha Fourth Hospital)
August 2023 - Present
Qibai Pingfei Granules Project (Various Hospitals)
August 2023 - Present
Certification
- Clinical Research Professional Certification
- Certified in Good Clinical Practice (GCP)
Positionapplied
Clinical Research Associate (CRA)
Personal Information
- Age: 31
- Gender: Female
Timeline
Clinical Research Associate
Beijing Bonowi Pharmaceutical Technology Co., Ltd.
08.2023 - Current
Clinical Research Associate
Beijing Excellent Future International Pharmaceutical Technology Co., Ltd.
02.2021 - 06.2023
Clinical Coordinator
Shanghai Baishida Pharmaceutical Technology Co., Ltd.
10.2018 - 02.2020
Bachelor of Science - Nursing
Hunan University of Chinese Medicine
- Clinical Research Professional Certification
- Certified in Good Clinical Practice (GCP)
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