View Cart

Certified Resume Writers | Professional Resume Writing Service ~ Starting at Only $99!

The sample below is for a Clinical Research Manager Resume. This resume was written by a ResumeMyCareer professional resume writer, and demonstrates how a resume for a Clinical Research Manager Candidate should be properly created. Our Certified Professional Resume Writers can assist you in creating a professional document for the job or industry of your choice.

Get Started Now!

CLINICAL RESEARCH MANAGER

Detail-oriented, accomplished, and articulate Clinical Research Manager currently pursuing Masters in Clinical Research, with more than 10 years overall research and academia experience with Vitreous-Retina-Macula Consultants of NY, and Vanderbilt and Columbia Universities. Demonstrate expertise in all facets of Phase I, II, and III clinical trials, IRB submissions, and other clinical trial submissions. Provided University of Maryland instruction in general chemistry, organic chemistry, and biochemistry to graduate and undergraduate students. Award winner for Clinical Research achievements, and published multiple papers and abstracts in professional scientific journals.

CORE STRENGTHS

 Project Management
 26 Clinical Trials
 9 Federal Research Grants
 Technology Savvy/EDC Proficient
 Regulatory Documentation
 IRB/FDA Submissions
 Neurocognitive CRF’s
 Lab Operations Procedures
 Research Subject Recruitment
 Develop Grant/Study Budgets

PROFESSIONAL HISTORY

Research Coordinator – Vanderbilt University, Nashville, TN 2010 – Present
 Effectively prepare and oversee regulatory document preparation for Vanderbilt Ingram Cancer Center Phase I, II, and III clinical trials (industry & investigator initiated).
 Prepare IRB submissions, consent forms, billing templates, clinical trial Web content, and regulatory site files for cancer clinical trials.
 Develop study documents; garner consents from study patients, schedule study patient visits and clinical procedures.
 Effectively complete SAE paperwork and files documents with sponsor, IRB and FDA, and accurately review and maintain study-specific documentation.
Research Officer – Columbia University, Neurology Dept., New York, NY 2008 – 2010
 Established and maintained relationships with investigators, sponsors, site personnel, and oversaw daily clinical trial operations within core neurocognitive laboratory.
 Oversaw and monitored trial sites for study protocol adherence and SOPs, and provided appropriate verbal and written feedback to clinical research sites.
 Managed overall site performance, deficiencies and corrective action required, and oversaw neurocognitive administration quality control.
 Reviewed all trial site neurocognitive CRF’s, and created core lab standard operating procedures.
 Oversaw evaluation of neurocognitive exams and electronic data capture, and effectively administered neurocognitive assessments.
 Organized all neurocognitive training meetings, and effectively trained new neurocognitive examiners.
 Screened and enrolled study subjects, and interacted with study subjects during study visits and recruitment
Clinical Research Consultant -Vitreous-Retina-Macula Consultants of NY, New York, NY 2008 – 2009
 Managed all pre- and post-awarded financial activities, and successfully generated and reviewed grant and study budgets.
 Oversaw all research financing and allocation, and provided professional expertise regarding on-site clinical research project specifics.
Clinical Research Manager – Vitreous-Retina-Macula Consultants of NY, New York, NY 2007 – 2008
 Managed Phase I, II, & III Clinical Trials from pre-initiation to closeout, and strategically directed pre- and post-award financial activities.
 Effectively recruited, trained and developed on-site research staff, and provided supervision of clinical research coordinators and research assistants.
 Established and maintained relationships with investigators, sponsors, and site personnel.
 Reviewed and created grant and study budgets, IRB documents and numerous other clinical trial submissions. Negotiated budgets with sponsor representatives, and focused on design and writing of case report forms and informed consent forms for clinical trials.

 Directed design, implementation and monitoring of clinical trials, preparation of INDs and periodic study reports for New Drug Applications, and ensured (GCP) was maintained.
 Ensured proper storage, dispensation, and accountability of clinical trial supplies including investigational agents.
Clinical Research Coordinator – Columbia University, New York, NY 2005 – 2007
 Managed all facets of Phase I, II, and III Clinical Trials, hired all trial subjects, interacted with all study subjects during study visits and recruitment, and created grant and study budgets.
 Prepared manuscripts for scientific journals.
Research Laboratory Manager -University of Maryland, Baltimore MD 2002 – 2004
 Planned research projects and developed a timetables, budgets and resource analysis for assigned studies.
 Oversaw project for NIH, DOD, and industry related projects.
 Assisted in writing annual reports, grant proposals, and academic papers. Managed and monitored laboratory personnel, safety and radiation safety protocols.
 Ensured proper storage, dispensation, and accountability of research supplies for various study protocols.
 Oversaw Dosimetry accountability, and successfully maintained cancer and endothelial cell lines.
 Assisted in animal necropsy and Imaging, and managed all aspects of daily laboratory operations.
Lecturer – Department of Chemistry and Biochemistry, University of Maryland, Baltimore, MD 1999 – 2002
 Provided University of Maryland instruction in general chemistry, organic chemistry, biochemistry to more than 1,200 graduate and undergraduate students, and served as staff liaison between faculty and laboratory instructors.
 Prepared educational materials, and trained graduate students for teaching assistantships.
 Evaluated and mentored university guided study directors, and efficiently managed daily operations, coordinated personnel, oversaw laboratory sessions, maintained records and scheduling for the evening Chemistry science enrichment program.

EDUCATION
M.S., Clinical Research – George Washington University – Pending 2011 GPA 3.87
B.S., Biology – Emory University, Atlanta, GA – 1996

AWARDS / CERTIFICATIONS / AFFILIATIONS
Tuition Award – George Washington University 2011
Certified Clinical Research Professional, SoCRA 2008 – Present
Certified Clinical Research Coordinator, ACRP 2008 – Present
Member – Association of Clinical Research Professionals 2007 – Present
Member – Society of Clinical Research Associates 2007 – Present

PUBLICATIONS
S Amin-Hanjani, L Rose-Finnell, D Richardson, S Ruland, D Pandey, KR Thulborn, DS Liebeskind, GJ Zipfel, MS Elkind, J Kramer, FL, Silver, SE Kasner, LR Caplan, CP Derdeyn, PB Gorelick, FT Charbel and VERITAS Study Group. Vertebrobasilar Flow Evaluation and Risk of Transient Ischaemic Attack and Stroke study (VERITAS): rationale and design, International Journal of Stroke, 5 (6): 499-505 (2010).
Amitava Mitra, Justin Mulholland, Anjan Nan, Edwina McNeill Hamidreza Ghandehari and Bruce R. Line, Targeting Tumor Angiogenic Vasculature using Polymer-RGD conjugates, Journal of Controlled Release, 102 (1): 191-201 (2005).
Amitava Mitra, Anjan Nan, Hamidreza Ghandehari, Edwina McNeill, Justin Mulholland and Bruce R. Line, Technetium-99m Labeled N-(2-Hydroxypropyl) Methylacrylamide (HPMA) Copolymers: Synthesis, Characterization and In Vivo Biodistribution, Pharmaceutical Research, 21 (7): 1153-1159 (2004).

Order From Us Securely at ResumeMyCareer.com