Kenisha Baker
Senior Clinical Research Associate 1 @IQVIA
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WORK HISTORY
Senior Clinical Research Associate 1 @IQVIA
US
EDUCATION
Temple University
Bachelor of Science (B.S.), Kinesiology
University of Pennsylvania
Post Baccalaureate, Microbiology, General
Abington Senior High School
Diploma
Fox School of Business at Temple University
Master of Health Administration, Health/Health Care Administration/Management
ABOUT KENISHA BAKER
Dedicated Senior Clinical Research Associate with a passion for driving excellence in clinical studies and advancing patient-centric clinical trials. Deadline-driven multitasker who thrives in a large-scale, fast-paced environment and collaborates seamlessly with a close-knit team of highly qualified CRAs. I consistently meet project timelines while efficiently managing multiple concurrent projects. My unwavering commitment to research protocol compliance, including strict adherence to regulations and principles of ICH-GCP and FDA standards, ensures patient safety and research integrity. I have a proven track record in identifying, selecting, initiating, and closing-out investigational sites for clinical studies in phases II – IV, fostering cross-functional teamwork, cultivating relationships with key opinion leaders, clinical site staff, and healthcare professionals. Expertise in Key Therapeutic Areas: My expertise spans essential therapeutic areas, including:Phase 2a-4 Metabolic/ObesityDermatology Proteinuric Kidney Disease Hepatocellular CarcinomaPain trials Sarcoma Rare Disease & Peri-Operative Prostate Cancer Metastatic Cancer Hematologic Malignancy Car-TMaternal and Fetal Health Proficient in Industry-Leading Tools: Judi AG MednetIqvia Central Lab Q2 SolutionsIQVIA Study HubReal Time CTMS eClinical CTMS TrialMax GreenphireERT GlobalSitesFirstLabcorpTrifecta Safety VigilanceEPICSharepointLong Boat IWRS: Suvoda Advarra IRB PlatformeTMF Management: Veeva Vault, Vault Clinical, Medidata RAVE EDCPreclarus Central LaboratorySite Regulatory: Complion, Circuit Clinical, FlorenceKey Competencies- Independently sets up and monitors studies, completing reports with meticulous attention to detail. Site Management- Expertise in preparing regulatory submissions and maintaining compliance throughout the study lifecycle- Skillful at balancing sponsor-generated queries and ensuring timely resolutions- Takes ownership of study cost efficiency, optimizing resources without compromising quality- Contributes to training and mentoring initiatives, fostering professional development among fellow CRAs.Career Goals:Passionate about making impactful contributions to clinical research at multiple clinical operational levels and continuously enhancing skills in study management and site coordination. Open to exploring new challenges and opportunities for professional growth.
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