Cllinical Research Coordinator/Rearch Assistant

JASMYN ADAMS

**** ********** ******, *******, ** 30013

678-***-**** * *********@*****.***

Clinical Research Coordinator / Research Assistant

Highly motivated candidate with expertise as a contributing member of a clinical research team focused on Phase I-IV trials, with broad knowledge of scientific investigative methodologies. Eager to translate expertise gained in research to measurable success in a career role with a dynamic corporation. Well versed in a variety of therapeutic disciplines, including Oncology, Cardiology, Pain Management, Infectious Diseases, Autoimmune Disorders, and Gastroenterology. Offers a demonstrated record of success in multiple research settings, including hospitals, medical offices, and laboratories. Capable of delivering outstanding results with the highest degrees of skill and professionalism.

AREAS OF EXPERTISE

Clinical Research * Scientific Research * Data Collection * Data Summary Reporting * eDC Systems

Phase I-IV Clinical Trials * Scientific Investigative Methodologies * Regulatory Document Formats

Medical Terminology * GLP * GMP * GCP/ICH, IRB, FDA Standards

PROFESSIONAL EXPERIENCE

SOUTHEAST REGIONAL RESEARCH GROUP, Savannah - GA

Clinical Research Coordinator Intern, Feb 2013

Gained invaluable knowledge of the principles of clinical trials, research, and study design at this clinical research trial management organization. Provided critical support to the determination of patient eligibility for clinical trials and the informed consent process, while creating patient research binders. Engaged in the production and review of source documents. Developed insight and knowledge into the protocols applicable to active and upcoming studies.

Key Accomplishments:

* Entrusted with timely and proper set up of all sponsor-supplied research equipment.

* Leveraged superior technical skill and subject matter expertise to assist Clinical Research Assistants in all study-related tasks.

* Updated and maintained all Electronic Case Report Forms (eCRF), furnishing missing pages to ensure completeness and accuracy.

ROCKDALE MEDICAL RESEARCH ASSOCIATES - Conyers, GA

Study Coordinator Intern, Oct 2012 – Feb 2013

Collaborated extensively with the Project Manager and members of the project team to ensure the successful launch, maintenance, reporting, and closure of clinical trials for this study site performing clinical trials of new medical treatments. Tasked with the recruitment of study participants, gathering informed consent while preparing source documents and study binders, accompanied by the ongoing collection of data through interviews and patient examinations. Engaged in the preparation of lab kits and packaged biological specimens in full compliance with all shipping and handling protocols.

Key Accomplishments:

* Cultivated multiple channels of communication with a network of federal agencies, sponsors, principal investigators, study subjects, and site personnel.

* Ensured strict compliance with all regulatory and sponsor-provided guidelines and protocols governing the collection and tracking of clinical data, while integrating all query responses into clinical databases.

UNIVERSITY OF NORTH CAROLINA

LINEBERGER COMPREHENSIVE CANCER CENTER - Chapel Hill, NC

Research Assistant, Aug 2009 – Apr 2012

Directed all aspects of research data management at this cancer research and treatment center, closely tracking and reporting the progress of multiple ongoing studies. Seamlessly executed a broad spectrum of administrative and clerical functions in support of research studies, while remaining in compliance with all regulatory requirements and standards. Provided oversight of multiple concurrent projects, dynamically adjusting strategies to match changing timelines and priorities. Coordinated all aspects of collaborative efforts with hospitals, physicians, project managers, investigators, and other research personnel.

Key Accomplishment:

* Fulfilled a key role as hands-on technician in the performance of molecular biology assays, including DNA isolation, DNA sequencing, PCR amplification, protein purification, and Western blots.

PARION SCIENCES INC. - Research Triangle Park, NC

Research Technician Summer Intern, Apr 2009 – Aug 2009

Leveraged superior subject matter expertise and organizational skill to provide technical and administrative support to investigators and senior study personnel at this development-stage pharmaceutical company focused on the discovery and development of new treatments for serious diseases. Assembled study data into data summary reports, while reviewing regulatory documentation for accuracy and completeness.

Key Accomplishment:

* Successfully completed Parion Sciences Training Program ahead of schedule, demonstrating the ability to comprehend and apply new concepts quickly.

UNIVERSITY OF PENNSYLVANIA SCHOOL OF MEDICINE - Philadelphia, PA

Research Specialist, Aug 2007 – Apr 2009

Cultivated relationships of collaboration and cooperation with scientists, physicians, and research personnel engaged in the performance of scientific research studies. Engaged in extensive data entry and review, while producing data summary reports. Contributed to the successful collection and transport of blood samples, while ordering equipment and supplies as needed.

Key Accomplishment:

* Gained invaluable experience performing molecular biology assays that included DNA sequencing, DNA isolation, PCR amplification, protein purification, and Western blots.

SILLIKER LABORATORIES OF GEORGIA - Stone Mountain, GA

Microbiology Technician (Contract), Mar 2007 – Aug 2007

Exercised advanced technical proficiency in Laboratory Information Systems (LIMS) to manage and track research data for this provider of practical solutions to food safety, quality and nutrition challenges throughout the supply chain. Ensured adherence to Standard Operating Procedures, as well as GLP and FDA regulations.

Key Accomplishment:

* Assumed a lead role directing the actions of small teams in reviewing files and logging outstanding data discrepancies.

PRIOR WORK HISTORY

Pharmacy Technician, Walgreens Pharmacy, Loganville, GA (2006 – 2007)

Student Intern, Tulane Hospital, New Orleans, LA (2003 – 2006)

EDUCATION

* University of North Carolina at Chapel Hill, Chapel Hill, NC, Master of Science in Pharmacology

Thesis: Validation of PAK Kinases for the Development of Novel Therapeutics for Pancreatic Cancer Treatment

* Xavier University of Louisiana, New Orleans, LA, Bachelor of Science in Biology

PROFESSIONAL DEVELOPMENT & TRAINING

* Workshops: Mentoring & Leadership Skills (2011), Ethics Training (2009), Quantitative Skills (2010), Scientific Writing (2009), Scientific Presentation (2009)

* Southeast Regional Research Group: Collaborative and Initiative Training (Citi), ALCOA Training, EDC Training, IVRS/IWRS Training, Invivodata EPX ePRO Management System Training

* Rockdale Medical-Research Associates: ICH/GCP Training, EDC Training, AE & SAE training, OSHA training, HIPAA training

* UNC Eshelman School of Pharmacy: Quantitative Methods in Clinical Research, 2010

* GCP Guidelines Training (Citi Training Program), 2013

* IATA Training (Citi Training Program), 2013

* Intro to Clinical Drug Development Process: ICH/FDA GCP for Clinical Trial Sites, 2013

* Rave EDC Essentials for CRCs, 2013

* Rave EDC Essentials – All Roles 1: Rave EDC Basics, 2013

* Investigator Site Training Completion Form for OC RDC (SITE) Training, 2013

TECHNICAL PROFICIENCIES

* EDC Systems (Phase Forward Inform, BioClinica Express, Medidata Rave, Oracle, Datalabs)

* Microsoft Office (Word, Excel, PowerPoint, Access, Outlook); SAS, Adobe

* Clinical Trial Management Systems (Clinical Conductor)

* Project Management Software (Basecamp)

JASMYN ADAMS, Page 2

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