Clinical Trial Recruitment Success

Superstar Clinical Trial Recruiter becomes successful entrepreneur!
By: Clinical Trial Resource LLC
 
ORLANDO, Fla. - Nov. 17, 2017 - PRLog -- Intro

Licensed Clinical Social Worker (LCSW) Amanda Secran manifests adherence to detail, strong communication skills and years of recruiting experience into another successful business. Clinical Trial Resource (CTR)is poised to meet and exceed study contract consent and randomization goals with the development of a proficient and systematic way to recruit, consent, and randomize patients for research sites nationwide.

Brief Background

After working for 15 years as an LCSW, Amanda took a leap of faith and ventured into the world of clinical research without any industry experience. The challenges endured fueled her to become the number 1 recruiter at every site she worked at. She met and exceeded contract goals without a database, utilizing primarily local area networks and community resources. This recruitment expertise encouraged her to venture out and start her first company Consent2Randomize. C2R had incredible success right off the ground. The company credits itself with an amazing 1600 consents for a major Pharmaceutical company in under 8 months! Riding high on that level of Success Amanda decided to take recruitment to the next level with Clinical Trial Resource.

Details about CTR

Clinical Trial Resourceis Amanda's latest venture. CTR teams personalized site recruitment with technology base systems to track metrics, direct traffic flow toward a web base patient portal and continuously run campaign ads via social media/internet. CTR offers the implement a recruitment system that Amanda believes is the core value of her company's success. "The recruitment system and processes are built upon key research components. These components are an intricate part of CTR core values" The Continuous focusing on quality, reliability, good data and accountability benefits both researcher and participant throughout the screening process with the end goal – a sign consent.

CTR offers clinical research sites and CRO's the following recruitment services:

·         Online and Mail-Out Marketing Campaigns- Sponsor and IRB approved

·         Lead Capture and Follow-up

·         Design study specific I and E prescreen tool.

·         Verbal consent to document lead PHI, and medical history and preauthorization for site to enter information into their database.

·         Daily communication with site regarding cancellations and reschedules

·         Conducting 20-30 minute phone call to prescreen, qualify, and schedule allotted appointment times.

·         Ensuring good data with a clinical review of each prescreen against protocol I and E. Data review also requires pertinent participant information is documented.

·         The prescreen tool includes: patient demographics, medical history, medications and adherence to the inclusion/exclusion criteria

·          Prescreen tool sent to site 48 hours prior to participants scheduled appointment within a confidential communication system.

·         A minimum of three contacts with each participant is completed before their initial screening appointment. Contacts include

1.      Prescreening Particpant

2.      Educating participant on basic research, study compound, study design, and study commitment.

3.      Schedule initial office visit

4.      Confirming appointment with participant via phone call, text, email.

5.      Site name, date/time of appointment, address, and telephone number is communicated through participants chosen method.

Final Follow Through -Performance Based Payment Structure

Confident in our recruiting system, our clients pay only for qualified patients who consent and randomize.  Our recruiters are trained in a wide variety of indications. Our recruiting system offers up to 16 hours of daily coverage on some databases.

Contact Amanda at asecran@clinicaltrialresource.com for more information.

Website is http://www.clinicaltrialresource.com

Contact
Nick Mansilla
Amanda Secran
info@clinicaltrialresource.com
End
Source:Clinical Trial Resource LLC
Email:***@clinicaltrialresource.com
Posted By:***@clinicaltrialresource.com Email Verified
Tags:Clinical Trial Research Study, Clinical Trials, Research
Industry:Medical
Location:Orlando - Florida - United States
Subject:Companies
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Page Updated Last on: Nov 18, 2017



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