Job Summary We are currently seeking a full-time, office-based Clinical Safety Coordinator to join our team in Taiwan

Job Summary Medpace is currently looking for a Clinical Trial Manager (CTM) to lead global clinical research studies.

- Develop / implement product training materials and responsible for providing product training to the clinical

contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on

Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial

The Clinical Project Manager will play an integral role in providing clinical support by working closely with startups, the

territory sales & clinical case in the assigned accounts - Develops customer & accounts with strategic planning and execution

【Study/ site management】 ※ Plans, executes and oversees clinical trials to ensure timely completion of the investigation,

general guidance and direction from our Clinical Project Lead, Clinical Trial Manager, or designees. *May collaborate with

Support CRA for relevant clinical trial activities (including but not limited to IRB submission activity, submission

The Clinical Trial Assistant is responsible for: - Track, scan, code and upload documents to central filing system per the

1. Serves as global level project manager from sponsor end (perform and participate in project development process and CRO and vendors selection, review core document/procedure, etc.) 2. Meet country goals through project strategy planning/execution in collaboration with project members. 3. Ensure study conduction with speedy and good quality through project leadership with internal cross functional teams, CRO Oversight, Issue management, CRO oversight monitoring visit and etc. 4. Initiates and maintains relationships with Investigator according to assigned therapeutic area. 5. Support and lead country activity to enhance cross-functional department cooperation according to assignments. 6. Perform other duties as assigned.

into confident Clinical Specialists. Key responsibilities include acquiring comprehensive RM clinical knowledge through

CRA for BE study/New drugs/Medical devices 1.Clinical research study setup/study procedure setup/site staff training 2.

- At least 1-year clinical research experience (Oncology is a plus) - Independently responsible for submission, contract

Reporting to: Lab Director, or Lab Manager Position description: The Researcher is responsible for the conduct of analysis related works according to GCP, GLP, CAP, Standard Operating Procedures (SOP), applicable Study Specific Procedures (SSP), and local regulatory requirements. Manage the operation of MT and aid physicians in the diagnosis, treatment, and prevention of diseases by testing patient specimens, correlating data, and reporting results in a timely manner to effect quality patient care. Responsibilities: • Conduct analysis work following related SOPs and guidance. • Draft/check/review/approve documents, such as SOP, protocol, analytical result, report and method. • Involve in lab logistics (general affair) management, such as purchasing, inventory controlling, payment applying. • Responsible for instrument maintenances, workspace cleaning/maintenance. • Delegated /assigned as the system owner for computerized system, do the corresponding work for system, such as validation test, periodic review, report, etc. • Participate in CAP/GCP/GLP/ regulatory related training courses. • Provide temporary supporting assigned by line manager. • Involve in sample collection kit/label preparation. • Involve in analytical study project management. • Refer to additional Study Based Responsibilities while being assigned in GLP project. Qualifications: Education and Experience: • A 4-year BS (Bachelor of Science) degree in Biochemistry, Biotechnology and Laboratory Science, Chemistry, or a related field. Or Junior colleague with over 3-year lab work experience and well qualified. Advanced degree is a plus for Associate Researcher/ Senior Researcher. • License of Medical Technician is required for Associate Researcher/ Senior Researcher in Central Lab. Skills and Competencies: • Familiar with all lab operation activities. • Excellent working knowledge of CAP/GCP, applicable law (local and country) and regulatory requirements. • Good communication skills. • Good verbal and written English or other second language skills. • Good problem-solving skills. • Effective time management and prioritization skills.

- At least 3-year clinical research experience (Oncology is a plus) - English ability: frequent verbal/ writing

General Statement: The (Senior) Clinical Research Associate is accountable for managing and overseeing the execution of

Clinical Territory Associate will work closely with the Clinical Sales Manager to gain knowledge in all aspects of our

training materials • Provide administrative support for clinical trials/to Investigator Engagement (e.g., data entry,