- Maintained interactions with key stakeholders such as the local study team, external service providers, and other functional groups to ensure that the project is delivered with highest quality.- Lead/contributed to the preparation of delegated study documents (e.g. Informed Consent Form, master Clinical Study Agreement etc), and external service provider related documents (specifications, study specific procedures, descriptions, presentations etc.)- Proactively contributed to risk and issue identification, development of mitigation and/or action plans for identified risks and issues- Supported Global Study Leader (GSL) with budget management, clinical supply planning and tracking, lab specimen management, status reports, imaging data reconciliation, and start-up and close out activities.- Lead multiple studies and kept track of study timelines using project management tools.

- Supported Study Leader and Study Manager in preparing delegated study documents and coordinated the completion of study related plans such as the supplier oversight plan, study management plan, and Monitoring Plan.- Focused on project efficiency and adherence to project timelines and financial goals and tracked study performance metrics on a regular basis. Used risk management logs and trackers to identify deviations early on and took action accordingly.- Work with functional teams to ensure appropriate quality standards for the duration start-up, maintenance, and close-out, Shared lessons learnt and provided mentorship to colleagues.- Initiated vendor activities and had successful oversight of vendors involved with recruitment and retention activities and consistently identified risk and issues that may impact study delivery.- Initiate and lead the set-up of the electronic Trial Master File (eTMF). Maintain and close the eTMF to ensure compliance to International Conference of Harmonization Guidelines for Good Clinical Practice (ICH/GCP) and company SOPs - Set-up, populate and accurately maintain information in tracking and communication tools (e.g. CTMS, SharePoint, BOX, MS teams and study team shared mailbox) and support team members in the usage of these tools- Support the set-up, maintenance and close-out of Clinical Trial Transparency (CTT) activity in PharmaCM, coordinating with relevant stakeholders to fulfil compliance and meet the regulatory authority needs- Lead practical arrangements coordination and contribute to the preparation of internal and external meetings e.g. study team meetings, committee meetings, monitor meetings, Investigator meetings and virtual meetings. Liaise with internal and external participants and/or vendors- Work on non-drug project work in process improvements and/or leading improvement projects as discussed and agreed upon with their manager

- Managed research data using appropriate tracking systems such as IXRS, CTMS, etc. while complying with internal policies and ICH-GCP guidelines.- Lead multiple research projects from study start-up to closeout, coordinated with a large team and successfully met recruitment goals for all research studies on site.- Ensured accuracy of data by performing quality assurance checks and responding to queries in a timely manner.

- Performed daily quality assurance checks on treatment machines, room equipment, and patient data.- Coordinated with a diverse hospital team to ensure that patient’s chart of in order and that the patient received optimal care.- Liaised with stakeholders to prioritize areas of research, test feasibility of ideas, and understand the scope of the topic area. - Coordinated with internal and external stakeholders to execute project activities while ensuring that all project guidelines were met.

- Managed multiple research projects at a time and ensured each project followed timeline and budget constraints.- Performed quality assurance checks to ensure accuracy of data and compliance of data with hospital policies and ICH-GCP guidelines.- Worked with research supervisor to create study specific tools and liaised with appropriate study members to address inconsistencies.

- Designed research study involving cancer patients and stored data in an organized, easy-to-analyze format.- Developed clinical protocols, completed IRB/REB application, and drafted Informed Consent Forms.- Worked with the research team to develop data analysis tools and ensured that project was within timeline and budget.- Conducted research that was in accordance to regulatory requirements.- Maintained detailed documentation of research findings and presented research in the form or a written report as well as oral presentation.