syed haider

Pharmaceutical professional skilled in Business Development, Regulatory Affairs, and Pharmacovigilance. Experienced in driving cross-functional collaboration and clinical trial projects, including review of clinical data, study protocols, budget management, and vendor management. Key strengths include project management, business relationship management, strategic planning, and regulatory compliance.

• Identifies, recruits, and schedules patients who may be eligible to participate in the oncology clinical research program such as breast, colorectal, lungs and blood cancers.
• Responsible for understanding, implement, and follows a interventional/observational study protocol and is able to conduct multiple studies such as Phase I, II, III and IV independently, obtaining training or training others to safely and accurately perform or assess required protocol procedures.
• Performs the initial assessment of potential patient participants, including but not limited to taking detailed clinical history, performing vitals and completing patient data forms.
•  Provides potential patient participants with study information. Obtains informed consent forms.
• Acts as the initial clinical resource and liaison between PI, nurses, and laboratory personnel.
•  Responsible for data management and data analysis. Ensures data entry is accurate and completed in a timely manner.
• Responsible for the initiation, organization, and handling of patient follow‐up. Assesses and analyzes patient monitor data at all follow‐up visits.
• May attend various meetings pertaining to the oncology clinical research program. May present information at the meeting.

Master in Pharmacology