Download Webinar Slides and Recording

More about the webinar

© 2016 marcus evans webinars

Our panel of speakers

With over 16 years in the pharmaceutical industry Shaheen Limbada brings extensive experience in organizational development and execution, patient recruitment and retention, clinical study conduct and governance. Most recently Mr. Limbada was the Head of Clinical Operations – North America for LEO Pharma, responsible for all clinical trials conducted across the continent.  Currently, as a co-founder and Managing Director of Topstone Research, Mr. Limbada is responsible for the overall conduct and governance of all Trial Management processes, playing a hands-on role in the planning and execution of functional services. In addition he manages the day-to-day affairs and the strategic direction of all three divisions of Topstone Research Inc, including financial and operational matters.
 

 

Shaheen Limbada
Managing Director
Topstone Research Inc.
 

Patient RecruitmentHow to achieve your recruitment goals on time, everytime!

Complimentary Webinar

in partnership with

Patient recruitment continues to be the number one reason for study delays. It is estimated for everyday a drug is not on the market, 1 million USD is lost in revenue, more importantly, patients suffering from illnesses are left waiting for products that can help them achieve their heath goals or provide a better quality of life.
 
This webinar examines techniques used to ensure on time patient recruitment initiatives including the following:
 
- The feasibility process- what questions to ask to ensure you are selecting the best sites for your program.
- Site engagement and why it's critical to the success of your study and how to achieve it.
- Digital media strategies 
- Patient centricity- How to incorporate the patient voice into your clinical trials.
 

Feasibility Process

Site Engagement

Digital Media Strategies

Patient Centricity

Jacquie Mardell has 35 years of pharmaceutical and biotech industry and education experience. She has a broad background in planning, implementing, monitoring and analyzing clinical development programs, has led teams in the execution of clinical programs in a wide variety of therapeutic areas in industrialized and emerging countries, and has contributed to several successful product registrations. She was the instructor for Good Clinical Practice and elective courses at UC Santa Cruz extension certificate program on clinical trial design and management.

Jacquie Mardell
Sr Director Clinical Operations
Ascendis Pharma