Rida Haider Email & Phone Number

Rahway, New Jersey, US

Durham, North Carolina, US

Morrisville, NC, US

Dublin, IE

Cambridge, Cambridgeshire, GB

- 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.

Cambridge, Cambridgeshire, GB

- 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.

Toronto, Ontario, CA

- 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.

London, Ontario, CA

- 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.

London, Ontario, CA

- 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.

Hamilton, Ontario, CA

- 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.