Pearl Pathways Hires Masheka Fuqua
Experienced clinical research associate joins Pearl Pathways
INDIANAPOLIS, INDIANA – May 18, 2017 — Pearl Pathways announces the hiring Masheka Fuqua as a Clinical Research Associate serving biopharmaceutical, medical device, and diagnostic life science companies.
Fuqua brings over a decade of clinical research experience to Pearl Pathways, including the coordination, management, and submissions of clinical trial activity across many therapeutic areas of research. Her decade of industry experience involves roles within clinical and healthcare market research at other organizations, including direct work with sponsors, sites, and clinical research organizations (CROs). Fuqua’s in-depth understanding of FDA, ICH, and Good Clinical Practice regulations coupled with her strong clinical background and acumen in auditing and monitoring various regulatory documents make her a strong addition to the team. Masheka holds an MS in Health Science from Indiana State University, a B.S. in Business Management from Indiana Wesleyan University, and an A.A.S. in Funeral Service from Mid-America College of Funeral Service.
Diana Caldwell, President and CEO shares, “Masheka delivers strong, balanced, and uncompromising research administration skills with integrity and credibility. She deeply understands clinical study regulatory processes including IRB submissions. Our clients will benefit from her broad industry experience that encompasses all aspects of clinical research, from site to sponsor to CRO. We are thrilled to have Masheka join the team.”
About Pearl Pathways
Pearl Pathways is a comprehensive life science product development services company. Our experienced team is obsessed with expediting life science product development regulatory pathways. We have three business units to serve you:
Pearl IRB is a full service commercial Independent Review Board that provides human research IRB reviews, IRB exemptions and waivers, and also offers support for research protocol/ICF medical writing, site assessments, and monitoring services.
Pearl ReGXP is a regulatory and quality compliance consulting practice that provides regulatory filing guidance, conducts global health authority negotiations, develops/improves quality systems, and delivers GMP/GLP/GCP auditing services.
Pearl IDEAS provides strategic product development assistance, third party vendor selection and management strategies, due diligence services, and sales and marketing services for drug, biologic and device companies.
To learn more, please visit us at www.pearlpathways.com, call us at (317) 899-9341, or email email@example.com. Pearl Pathways is located in Indianapolis, Indiana, and is AAHRPP accredited and a WBENC certified woman owned business. For media inquiries, contact firstname.lastname@example.org.