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Our Team Members have an average of 7 years experience in the industry. We require a minimum of two years specialized experience in a specific therapeutic are before they can work for you.
President
JeanMarie Markham, CCRA, RN
jmarkham@clinlogix.com
215.855.9054 ext. 201
As the founder and President of Clinlogix, LLC, JeanMarie Markham,
RN, CCRA, is an inspiring leader who seeks to continually drive
the field of Clinical Research Services forward. She has over 15
years of experience in the industry. In 1992, JeanMarie founded
Markham & Associates to provide regional Clinical Monitoring
and Investigator Management services to the Pharmaceutical Industry.
She personally developed a national platform of experienced Clinical
Research Associates to provide clients with regionally-based clinical
monitoring services in multi-therapeutic areas. These Clinical Monitoring
and Auditing services are now provided through CRA America, an affiliate
of Clinlogix.
In 1998, JeanMarie founded Clinlogix, a Clinical Research Service
Organization, with the mission of getting needed therapies and treatments
to the patients that need them by assisting the biopharmaceutical
industry through decreasing project cycle time and ultimately producing
timely, cost effective and high-quality clinical trial data. Loyal
clients can attest to the delivery of this vision, demonstrated
by Clinlogix’s early adaptation of EDC data management, among
other effective strategies to stay ahead of competing CROs.
JeanMarie is active in the Biopharmaceutical and Biotech industries
and also in her local community. She has served in her community
since 1998, as an elected member to the Executive Board of the Parent-Teacher
Association, where she was past President of the local chapter.
Executive Director, Sales & Marketing
Andrew Brailsford
abrailsford@clinlogix.com
Cell: +1.617.899.0782
Andrew has more than 15 years experience in the pharmaceutical industry and joined Clinlogix in May 2010.
During his career he has worked on business and product development activities in both drug discovery and regulated
environments using a multitude of techniques including Adaptive Clinical Trials, Mass Spectrometry, Liquid Chromatography
and Laboratory Informatics. Rewarding projects include
- Commercialization of a significant service line to drive the use of Adaptive Clinical Trials
- Product launches for real-time, large scale automation and integration applications
- Developing neonatal screening applications
- Enhancing the capabilities for agencies involved in Drugs of Abuse, Environmental Monitoring and Food Safety
With Clinlogix he is focused on delivering best in class services, to pharmaceutical, biologic and medical device
organizations, to conduct their clinical trials with a strong emphasis on quality, timeliness and budget.
Director, Project Management
Carrie R. Cameron
ccameron@clinlogix.com
Carrie has more than 10 years experience in the pharmaceutical and CRO industry. As Director of Project Management Carrie is the primary link between Sponsor and the Clinlogix team. Carrie's diverse experience and in-depth knowledge of the clinical trial process ensures that the Sponsors needs are paramount and is able to contribute to the planning and execution of the trial at all levels.
Carrie has been with Clinlogix for two years and has contributed to many of the processes and strong relationships we have with our Sponsors and Virtual Integration PartnersTM network.
Prior to joining Clinlogix Carrie worked as an Associate Director of Business Development and significantly grew the capabilities of an eClinical software organization.
Carrie's understanding and commitment to the Sponsor is driven partly from her 5 year tenure at Merck & Co., Inc. where she worked as a Financial Medical Program Coordinator supporting the outsourcing and financial management of clinical research studies.
Carrie is a graduate of Gwynedd-Mercy College with a Bachelor of Science Degree in Business Administration with a concentration in Organizational Management.
Senior Project Manager
Julie C. Cantwell, BS
jcantwell@clinlogix.com
As Senior Project Manager at Clinlogix, Julie's responsibilities include Study management encompassing Investigator Site identification, database development, and study start-up activities.
She effectively secures clinical trial opportunities and shares therapeutically aligned studies to solicit interest, perform feasibility, and facilitate access and availability of potential investigators and investigative sites.
With Clinlogix for over three years, Julie has worked as a liaison between Clinical Research Associates and sponsor companies on contracted projects. Additionally, she works with clients to ensure that the Investigative Sites and Principal Investigators are qualified and appropriate for our clients' specific project needs.
She comes to Clinlogix from Johnson and Johnson where she worked as a Pharmaceutical Sales Representative in their Ortho McNeil Neurologics division. She has 5 years of experience in business to business sales, including work for Office Depot.
A graduate of Bloomsburg University of Pennsylvania with a Bachelor of Science Degree in Computer and Information Systems, Julie has additional professional training in Project Management.
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