Randa Wahid

About Randa Wahid

Randa Wahid is a Senior Clinical Project Manager working on global clinical trials. She brings over twelve years of experience in the clinical research industry. She has managed clinical trial projects from phase I-IV within therapeutic areas of dermatology, metabolic, cardiovascular, neurology, and others. Randa has a Masters in Health Care Administration.

Experience

1. Senior Global Clinical Research Project Manager

   Indero (formerly Innovaderm)

   Oct 2021 — Present

   Proactively manages and communicates effectively with sponsors, study team members, functional departments, and senior management, with respect to site selection, vendor selection, project plans, trial budget and timeline management, quality standards and risk mitigation. • Controls the project budget by ensuring that project team member understand the hours allocation for each task and review time billed to the study against the budget to control write-off and identify out of scope activities for change orders.• Aids in development and maintenance of key project performance indicators for client specified metrics.• Leads study start-up process, including but not limited to conduct of the Trial Kick-off meeting the set-up of trial master file (TMF), site selection and finalization of site lists, site activation, management of vendor set up timelines and site contracting and budgeting.• Reviews and approves CRO, site, and vendor responses to quality assurance audits.• Provides project status updates ensuring compliance with the study budget, project scope and timelines.• Manages and reports on recruitment status and highlights initiatives needed to mitigate slippage in recruitment timelines • Plans and conducts Investigator’s Meeting.• Collaborates with the Regulatory Affairs group for central and local submissions of required essential documents.• Oversees clinical monitoring activities for site qualification, initiation, routine and close-out visits.• Supports the sites and ensures that each site has the necessary material to adequately perform the study.• Ensures the CRF complies with the protocol and Sponsor requirements and ensures queries resolution and data review process follow the study timelines until database lock. • In collaboration with relevant departments, prepares and delivers presentations for new business• Provides technical, therapeutic and project management expertise in training and process improvement efforts for the department.

Education

• California State University, Long Beach

  Master of Science, Health Care Administration

  2009 — 2012

• California State University, Fullerton

  Bachelor of Science, Health Science

  2004 — 2009

Skills

• Cpt
• Hospitals
• Microsoft Office
• Start-Ups
• Process Improvement
• Hcpcs
• CRO
• Access
• Good Clinical Practice (Gcp)
• Customer Service
• Medical Devices
• Clinical Research
• Ehr
• Clinical Development
• Marketing
• Insurance Billing
• Icd-9
• Healthcare
• Business Development
• Strategy
• Health Information Management
• Biotechnology
• Medical Terminology
• New Business Development
• CRO Management
• Clinical Trials
• Hipaa
• Healthcare Consulting
• Practice Management
• Life Sciences
• Pharmaceutical Industry
• Management
• Physician Relations
• Patient Satisfaction
• Microsoft Excel
• Physical Therapy
• Insurance
• Appointment Scheduling
• Product Development
• Medical Billing