A Research Data Coordinator is responsible for clinical data review and query generation, resolution, and reconciliation to support the delivery of clinical data. The job duties are listed on the Research Data Coordinator Resume as – performing administrative and coordinative work, designing, and reviewing assigned projects, entering study data into appropriate database and performing a review of discrepancy output and validation listings, reviewing and responding to queries to address problematic data identified during data review activities, and assisting local teal members with administrative activities as required.
The nature of the job demands the following skills and abilities – knowledge of clinical data and good clinical practices, knowledge of medical terminologies, proficiency with relational database management and software systems, strong spoken and written communication skills, excellent organizational skills, and a detail-oriented approach. A bachelor’s degree in a life science-related field is preferred.
Summary : Experienced healthcare and customer service professional, with strong organization and communication skills, looking to be part of a dynamic, teamwork environment.
Provided highly responsible administrative and patient care services for the support of three research protocols, and back-up coverage for multiple protocols.
Identified and interviewed eligible candidates.
Managed and maintained participant files, and study data via Excel spreadsheets.
Communicated regularly with investigators regarding recruitment and resolve any potential problems.
Liaisoned with patients, families, physicians, and other personnel.
Assisted in the preparation of information and reports for protocols, grants, and publications.
Coordinated the collection and storage, and shipment of specimens, films, and pathology slides to numerous external institutions.
Experience
10+ Years
Level
Senior
Education
Associates In Applied Science
Research Data Coordinator Resume
Summary : Experienced Research Data Coordinator professional, with strong organization and communication skills, looking to be part of a dynamic, teamwork environment.
Skills : MS Office, Mac Os, Mac Os.
Description :
Assisted with training newly hired Research Data Coordinators.
Interacted with the IRB as pertained to study protocol.
Translates from English into Spanish for non-English speaking patients.
Developed and maintained a system for controlling paper and electronic data flow for protocols and hospital policies, including records of surgery, pathology information, laboratory results, treatment dates, follow-up schedules, etc.
Prepared research folder for patients enrolled, assuring organization and timely addition of source documents as needed.
Ensured effective identification and recruitment of patients through regular, timely, appropriate screening, and consenting to and creating on/off study notes for minimal-risk protocols (e.g. PA or LAB studies) as assigned.
Consented patients to minimal risk protocols.
Experience
10+ Years
Level
Senior
Education
GED
Research Data Coordinator Resume
Summary : Over 25 years of experience in the medical field, results driven, highly dedicated to providing superb quality, efficient patient care while promoting wellness and support to all patients, family and staff. A highly-motivated, productive and customer-focused team player with strong communication, interpersonal, organizational, time management, analytical and problem solving skills.
Skills : Environmental Research, Inventory Management, Task and Time Management, Data Entry, Environmental Testing, Fashion Design.
Description :
Conducted pre-screening, recruiting, enrolling, and consenting patients to a high-risk longitudinal breast cancer biorepository lab study.
Collected and ensured the completion of patient study questionnaire according to protocol requirements.
Drawn study serial blood samples on patients as well as blood specimen drop-off to an appropriate research lab on a timely basis.
Maintained and ensured accuracy of data collection in electronic databases (Excel) and paper formats for study patient tracking purposes.
Composed medical transcriptions into Clinic Station for study entrance or study interim notes.
Registered all new patients into the institution database and obtains a copy of the accession number for case report shadow charts.
Prepared and submitted regulatory documentation into institution database for continuing reviews, amendments outlined per Institutional Review Board (IRB).
Experience
10+ Years
Level
Senior
Education
B.A. In Psychology
Research Data Coordinator Resume
Summary : Hold an MBA with a concentration in Project Management. During the time that I was pursuing my MBA, I created my own LLC to continue my passion for data analysis while being able to work at my own pace. I am a Data Analyst and Reports Developer with six years of experience working with data across multiple industries and two years of experience with reporting tools; Tableau and Alteryx.
Skills : Inventory Management, Protocol, And Medical Writing.
Description :
Coordinated the development and validation, implementation, assessment, and training for electronic data collection and management systems.
Coordinated the review of and analysis of abstract and manuscript submissions with authors, study sponsors, and biostatistics.
Prepared monthly reports detailing accrual, toxicity, response, etc for review by sponsor investigators and Clinical Trials Monitoring Committee.
Prepared reports for interim analysis of clinical trials which require formal data and safety monitoring boards.
Served as liaison with biostatistics core and database development team with regard to data collection, review, and analysis.
Designed electronic data capture requirements, electronic and manual data consistency checks, and data entry guidelines.
Planned and presented workshops on data collection to nurses and data managers as needed Document and reconcile serious adverse events, protocol deviations, and eligibility exceptions.
Experience
10+ Years
Level
Senior
Education
High School Diploma
Research Data Coordinator Resume
Summary : Research Data Coordinator professional with experience in pharmaceutical research trials, patient interaction, life-saving procedures, trial management, data collection, and clinical assessment completion, Possessing a strong sense of teamwork and interpersonal communications, along with a keen eye for detail and a passion for a positive patient experience.
Skills : Microsoft Outlook, InForm, Bioclinica, Medidata Rave, Oracle.
Description :
Extrapolated patient information from the electronic medical records, complete electronic case report forms and submit this information to research study sponsors.
Scheduled, prepared for, and actively participated in sponsor monitoring and auditing activities.
Responsible for research payout and tracking activities.
Coordinated patient follow-up visits.
Submitted scan images from local PACS system via upload through Perceptives or AG Mednet.
Assisted in the submission of serious adverse event reports to sponsors.
Obtained tissue samples from local pathology labs and submit to sponsor labs.
Experience
10+ Years
Level
Senior
Education
BS
Research Data Coordinator Resume
Headline : Past work experience in customer service, management, and research has given me the tools needed to communicate efficiently. I love to learn about everything and anything. I believe that having knowledge and understanding of how the world works, makes for a better team player and problem solver.
Skills : Proficient In C, C++, HTML, JavaScript, Visual Basic, Visual Basic Script, Basic, SAS, And Web Design.
Description :
Coordinated administration of clinical research protocols.
Maintained protocol database, related grants, and protocol reference materials.
Coordinated and reviewed new and existed research protocols.
Managed a database of clinical trial information and patient information.
Compiled status reports describing interim data.
Worked with leukemia subtypes section chiefs to keep the protocol list current.
Managed and trained new coordinators on protocols.
Experience
5-7 Years
Level
Executive
Education
MS
Research Data Coordinator Resume
Objective : Research Data Coordinator with 4 years of experience in Working closely with assigned research staff to provide support to Radiation Oncology clinical research trials by organizing, collecting, recording, and maintaining clinical data in an accurate and timely manner, providing all necessary support for the coordination and execution of research studies in the Department of Radiation Oncology.
Skills : Legal Research, Legal Terminology, LexisNexis, Westlaw, Drafting, Conflict Resolution, Negotiation, Contracts, Medical Records, Medical Terminology, Policy Development, Proposal Writing, Legal Research, And Writing.
Description :
Analyzed patient medical records for pertinent information per protocol.
Submitted research data for audits and review through sponsor and institutional databases.
Adhered to requirements stipulated by protocols, sponsor contracts, and all applicable laws and regulations regarding human subject research protections.
Recommended substantive revisions for incorrect or outdated Standard Operating Procedures for departmental records management and research monitor regulations.
Assessed departmental and institutional needs related to offsite storage, audit preparations, and space management and report findings to multiple departments to garner project support and ideas.
Represented department during institutional Clinical Research Lifecycle Design Project and presented ideas regarding study concept, initiation, and pertinent tools and resources.
Demonstrated excellent oral and written communication with patients, staff, and faculty.
Experience
2-5 Years
Level
Executive
Education
Juris Doctor In Law
Research Data Coordinator Resume
Objective : Highly personable and competent Medical Doctor with over 4 years of experience, Recognized for integrity, being compassionate, and excelling in diagnosis, Extensive experience in leadership, and as a team player amongst medical personnel.
Skills : MS Office, Research, Administrative, Data Entry, Customer Service, Computer, Event Planning.
Performed highly detailed data coordination for multiple protocols with strict deadlines.
Developed and implemented a training guide for new Data Coordinators.
Retrospectively reviewed charts for manuscript preparation.
Completed Clinical Research Training.
Attended Journal Club and Grand Rounds Department, Volunteer, for Food Bank of Houston annual food drive.
Responsible for lab collection and shipping for research studies.
Experience
2-5 Years
Level
Executive
Education
Master Of Science
Research Data Coordinator Resume
Headline : High-performing, strategic-thinking professional with more than ten years of experience in the health care industry. Working for a not-for-profit health plan that provided health care coverage to Medicaid and Medicare population, I had the opportunity to be involved in several projects surrounding the current health care system from the members, hospital, and provider perspective.
Accurated and efficient collection of data from various sources.
Demonstrated excellent oral and written communication with patients, staff, and faculty.
Processed, shipped, and handled collected specimens.
Verified information recorded to ensure the accuracy and completeness of all data reports.
Prepared for study monitoring visits and protocol audits.
Participated in the preparation and management of research budgets and disbursement.
Developed data management plans for sample design, sample storage, and study procedures.
Experience
5-7 Years
Level
Executive
Education
B.S
Research Data Coordinator Resume
Headline : Research Data Coordinator is responsible for Developing and maintaining a system for controlling paper and electronic data flow for protocols and hospital policies, including records of surgery, pathology information, laboratory results, treatment dates, follow-up schedules, etc, Preparing research folder for patients enrolled, assuring organization and timely addition of source documents as needed.
Skills : Data Coordinator, MS Office.
Description :
Informed and consented patients about study aspects and outcomes.
Assisted in investigational drug accountability.
Worked closely with study sponsors and CRO to maintain clinical research data FDA compliant, HIPAA compliant and aligned with Good Clinical Practices.
Coded adverse events, concomitant medications and other data as needed.
Responsible for monitoring trial stopping rules and providing status reports.
Prepared adequate supply of patient-ready packets per protocol as needed.
Developed (or assists as needed) and maintains detailed Excel spreadsheets and databases for the collection of research data, to include tracking, data entry, accrual, data auditing and screening log.
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