Clinical Data Coordinator Resume Samples

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LD
L Douglas
Lazaro
Douglas
5888 Pablo Hill
San Francisco
CA
+1 (555) 511 3535
5888 Pablo Hill
San Francisco
CA
Phone
p +1 (555) 511 3535
Experience Experience
Chicago, IL
Clinical Data Coordinator
Chicago, IL
Raynor, Ernser and Kozey
Chicago, IL
Clinical Data Coordinator
  • Works with team to identify quality improvement initiatives, implements improvement plans, monitors outcomes, and identifies opportunities for improvement
  • Provide data analysis and performance improvement consulting for large-scale healthcare quality assessment and improvement projects
  • Create test data, perform testing procedure of entry screens, and provide test results to the project lead or designee
  • Perform data entry in any clinical data management system used by Clinical Data Management
  • Assists in the development and testing of electronic databases
  • Assist in performing FIM competencies with other team members
  • Consults with managers, staff and physicians to support improvement activities and organizational initiatives
San Francisco, CA
Clinical Data Coordinator Temporary Position
San Francisco, CA
Moore LLC
San Francisco, CA
Clinical Data Coordinator Temporary Position
  • Assist in development and review of key performance indicators (KPI) and goals
  • Effectively manage DCF workload determined by TrialManager®
  • Manage, analyze, implement and verify Data Clarification Forms (DCF) submitted throuh the TrialManager®
  • Assisting in the application and interpretation of data to drive quality improvement efforts,
  • Assist in the resolution and response to issues and questions from client study team, physicians and site staff
  • Manage assigned project timelines and prioritization of tasks
  • Help to establish standard processes and procedures for department
present
Phoenix, AZ
Senior Clinical Data Coordinator
Phoenix, AZ
Okuneva, Stehr and Johnson
present
Phoenix, AZ
Senior Clinical Data Coordinator
present
  • Assist in developing and implementing new technology
  • Assist in development of Case Report Forms for assigned studies
  • Manage delivery of projects through full data management study life-cycle (with minimal guidance)
  • Perform comprehensive data management tasks including data review, writing and resolving data clarifications
  • Develop and maintain good communications and working relationships with CDM team
  • Working knowledge of ICH/GCP guidelines and FDA regulations
  • Independently bring project solutions to the CDM team
Education Education
Bachelor’s Degree in Science
Bachelor’s Degree in Science
Kaplan University
Bachelor’s Degree in Science
Skills Skills
  • Ability to exercise excellent attention to detail
  • Good computer skills, including working knowledge of Microsoft Office (Word, Access, Excel, and PowerPoint) and basic statistics
  • Ability to exercise independent judgment in doing medical summaries with strong analytical capabilities
  • Ability to adhere to detailed instructions
  • Coordinate the delivery of data management services for multiple projects, ensuring data integrity and quality deliverables on time
  • Applicable knowledge working with other clinical databases/EDC systems such as eClinicalOS, SAS
  • Excellent attention to detail
  • Strong client relationship management skills, and the aptitude to develop this further
  • Excellent organizational, communication, leadership and computer skills
  • Works with team to identify quality improvement initiatives, implements improvement plans, monitors outcomes, and identifies opportunities for improvement
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15 Clinical Data Coordinator resume templates

1

Clinical Data Coordinator Resume Examples & Samples

  • 0-3 Years Experience Level
  • Pharma research experience
  • Pharma experience preferred
  • Will be verifying data by cross-checking lists of records
  • MS Office experience
  • Experienced data management professional who is responsible for all activities relating to over 20 studies over the course of 1 year
2

Clinical Data Coordinator Resume Examples & Samples

  • 2+ years of Clinical Data Management or Clinical Research Associate experience
  • Proficiency in Microsoft Office Suite
  • Comprehensive data management/ QC expertise
  • Experience in auditing clinical data for accuracy and compliance
3

DRG / Clinical Data Coordinator Resume Examples & Samples

  • 3 years of inpatient medical chart coding experience
  • 5 years of Health Information Management/Medical Records experience in an academic medical center environment,
  • Prior experience as a DRG Coordinator,
  • Experience with 3M, RHIA or RHIT certification
4

Clinical Data Coordinator Resume Examples & Samples

  • Assist in the completion of protocol specific documents. Obtain relevant medical information from patient clinic charts/medical records. Maintain logs/progress reports to track both currently enrolled as well as follow-up participants. Provide protocol specific study documentation required in the management of study patient as per the protocol, federal regulations, and sponsor requirements and as required
  • Under the supervision of the Principal Investigator. Determine data to be collected and develop forms for collecting/summarizing data. Enter data onto case report forms and/or into computer database as appropriate. Complete corrections/queries required at audits/monitor visits. Ensure data integrity and consistency in computer database and written records
  • Assist the Clinical Study Coordinator for the entry of and maintenance of the patient calendar. Ensure protocol specific data is entered into Velos
  • Enters data onto case report forms and/or into computer database. Completes corrections/queries required at audits/monitor visits in a timely manner. Ensures data integrity and consistency in computer database and written records by reviewing entered data for accuracy
  • Query data inconsistencies and revise case report forms in compliance with standard operating procedures, Institutional, Federal and Regulatory guidelines
  • Actively participates in monitoring visits/site audits, etc. Seek review and approval of the Principal Investigator
  • Assist the Clinical Study Coordinator to maintain screening, enrollment, adverse event, deviation, tumor measurement, concomitant medication, delegation and other sponsor and/or protocol specific logs
  • Ensures that randomization and registration of patients are performed in compliance with CRS and UM policies, the protocol, ICH-GCP, and federal regulations
  • Provides support with study related procedures as required, i.e., EKG, laboratory and tumor assessment studies
  • Ensures work environment is organized and functions efficiently. Participates in a collaborative, empowered work environment as demonstrated through teamwork. Demonstrates a level of professional practice that supports the delivery of appropriate care and positive working relationships throughout the medical center
  • Engage in continuing education of research policies/guidelines. Maintains professional growth and development through seminars, workshops, and professional affiliations to keep abreast of latest trends in field of expertise
5

Clinical Data Coordinator Resume Examples & Samples

  • Education: Associate's degree (A.A./A.S.) or equivalent in a scientific, computer, or related discipline. Bachelor's degree preferred
  • Experience: 1 year related experience in clinical data management
  • Other: Some experience with relational databases preferred. Demonstrated knowledge of the conduct of general data management and data management quality control activities for a clinical study
  • Review study-specific documentation as part of the project team in order to obtain understanding of study-specific data processing conventions
  • Prepare data for entry through completion of transmittal verification, data tracking, and completion of manual review processes
  • Perform data entry in any clinical data management system used by Clinical Data Management
  • Reconcile project files and other documents generated in data management against a database for accuracy and completeness of data management processes
  • Investigate and resolve data anomalies
  • Identify the need for and generate data queries at any point during data processing, based on guidelines set forth in the Data Management Plan (DMP)
  • Issue and review queries for completeness and forward to the project lead or designee
  • Conduct quality control including case report form to database review processes
  • Create test data, perform testing procedure of entry screens, and provide test results to the project lead or designee
  • Work concurrently and accurately on multiple protocols
  • Provide functional oversight of data processing activities including training of Data Entry and CDA I staff on project specific tasks
  • Report routine project status and data trends to project lead or departmental management as required
  • Create case report forms in accordance with the protocol and established standards when necessary
  • Author portions of the DMP as required
  • Serve as resource for project lead and departmental management
6

Clinical Data Coordinator Temporary Position Resume Examples & Samples

  • Manage, analyze, implement and verify Data Clarification Forms (DCF) submitted throuh the TrialManager®
  • Effectively manage DCF workload determined by TrialManager®
  • Implement assigned project timelines and prioritization of tasks
  • Assist in the resolution and response to issues and questions from client study team, physicians and site staff
  • Conduct site and sponsor archival processes during study decommissioning
  • Act as CDM resource person for internal teams
  • Update of Maintenance Guides
  • Ongoing knowledge of study activities, protocol updates, data requirements and relationships to facilitate DCF verification and implementation
  • Review and update maintenance guides with internal team
  • Develop study specific data management plans as required by the client
  • Assisting in the application and interpretation of data to drive quality improvement efforts,
  • Collaborate with internal and external resources to ensure consistency of methods, interpretation and approach
  • Assist in development and review of key performance indicators (KPI) and goals
  • Manage assigned project timelines and prioritization of tasks
  • Help to establish standard processes and procedures for department
  • Lead and conduct site and sponsor archival processes during study decommissioning
  • Train new team members
  • Clinical background or experience in a healthcare field, pharmaceutical vendor or technology firm preferred
  • Experience with ad-hoc query tool (SQL, SAS) preferred
7

Clinical Data Coordinator Resume Examples & Samples

  • Extract data from source documents
  • Complete electronic Case Report forms in the RedCap database
  • Assist team with the creation of source document tools
  • Assist in reporting of data for quality and research projects
  • Assist in the creation of new databases and transition of databases to new platforms
8

Early Talent Clinical Data Coordinator Resume Examples & Samples

  • The person may serve in the role of back-up to a Data Operations Coordinator or Data Team Lead
  • To lead database audit team
  • To develop and test databases and edit specifications
  • To perform other duties and directed by the Data Operations Coordinator or Functional Manager
  • To meet objectives as assigned
  • To develop and maintain good communications and interpersonal relationships with the team
  • Ability to exercise excellent attention to detail
9

Senior Clinical Data Coordinator Resume Examples & Samples

  • Minimum four (4) years relevant work experience with increasing responsibility in data management with knowledge of two (2) or more therapeutic areas
  • Demonstrated time management skill and ability to adhere to project productivity metrics and timelines
  • Excellent oral and written communication skills and demonstrated presentation skills
  • Knowledge of clinical trial process and data management, clinical operations, biometrics, quality management, and systems applications to support operations
  • Working knowledge of the relationship and regulatory obligation of the CRO industry with pharmaceutical / biotechnological companies
  • Potential ability to lead by example data management staff
  • Demonstrated ability to work in a team environment and collaborate with peers
  • Demonstrated interpersonal skills
10

Clinical Data Coordinator Resume Examples & Samples

  • Responsible for the entry of data into electronic databases
  • Performs verification and validation of data entry
  • Sets up and maintain filing systems
  • Report data that is unreadable or not logical
  • Assists in the development and testing of electronic databases
11

Senior Clinical Data Coordinator Resume Examples & Samples

  • Serve as Data Operations Coordinator (DOC) for one or two global studies with fewer than 10 operations staff (excludes DE), or serve in a leadership role to a specific DM Task
  • With guidance from DTL or Manager, manage project timelines and quality; determine resource needs; identify out-of-scope work
  • Serve as Data Operations Coordinator or Data Team Lead (with guidance)
  • Perform comprehensive data management tasks including data review, writing and resolving data clarifications
  • Perform database designer activities for technologies not requiring extensive programming
  • Solve issues through using the global issue escalation/communication plan
  • Assist in developing and implementing new technology
  • Develop and maintain good communications and working relationships with CDM team
  • Interact with CDM team members to negotiate timelines and responsibilities
  • Good understanding of clinical drug development process
  • Background in Medical Terminology, Pharmacology, Anatomy, and Physiology
12

Clinical Data Coordinator Resume Examples & Samples

  • Data and Query Review
  • Team player with ability to work with technical and clinical team members
  • Ability to interact with CRAs and other key members of the team
  • Comprehension of clinical study documents (CRF guidelines, protocol, etc.) and SOPs and Working Practices
  • Efficiency and organizational skills to meet deadlines
  • Effective Interpersonal skills
  • Good communications skills, verbal, written and listening
  • Willingness to learn new things
  • Administrative Organization (such as being able to organize/save emails appropriately, etc.)
  • Ability to adhere to detailed instructions
  • Logical thinking ability in regards to Problem-solving skills
  • Proficiency in computer applications: Windows, Excel, Word, Outlook etc
  • Work independently with limited oversight
  • Very little physical effort required to perform normal job duties (unless otherwise indicated)
13

Clinical Data Coordinator Resume Examples & Samples

  • Supporting data entry for clinical studies
  • Ensure the data is entered accurately and according to ICH GCP guidelines and maintain overall data quality for assigned studies
  • Maintain relevant information and data for Trial Master File TMF assigned studies
  • Bachelor's degree in health or science (Computer Science, Engineering, Biological Science)
  • 1 year experience performing data entry (Manager will look at internship experience)
  • Strong background in health-care setting: Physician office, hospital, laboratory, or clinic
  • Strong working knowledge of Excel or sheets (Must be able to perform v-lookups)
  • Ability to work independently with minimum supervision
14

Clinical Data Coordinator Resume Examples & Samples

  • Positions in this function include operating data entry devices to perform a variety of data entry duties across functions
  • Review collected data to ensure information is accurate and complete
  • Seek clarifications or corrections to data from relevant stakeholders (e.g., return missing/incorrect documents to submitters; contact stakeholders to gather additional data)
  • Ability to type 40+ WPM
  • Quality Improvement/Quality Assurance experience
  • Provider enrollment experience
15

Clinical Data Coordinator Resume Examples & Samples

  • Perform data review and edit checks. Issue queries to sites, central laboratories, monitoring CROs, and/or Clinical Operations, and apply updates to database as identified through query resolution, data review, etc
  • Provide test, header and production data to internal/external stakeholders according to data specifications. Ensure data delivery timelines for TSB are met
  • Monitor Central Lab compliance with TSB standards/ specifications, and escalate issues as necessary
  • Actively participate in TSB continuous process and quality improvements
  • With understanding of TSB internal practices and policies, work with peers to problem solve and strategize to resolve issues to ensure study timelines and objectives are met
  • Position and management of systems is complex and errors in judgment would have a serious impact on the organization. Failure to achieve results or erroneous decisions or recommendations may cause delays in program schedules
16

Clinical Data Coordinator Resume Examples & Samples

  • 5 years of Health Information Management/Medical Records experience in an academic medical center environment
  • Prior experience as a DRG Coordinator
  • Experience with 3M
  • RHIA or RHIT certification
  • 3 years of inpatient coding experience
  • CCS certification from AHIMA
  • Strong interpersonal and coder education expertise skills are essential to succeed
17

Clinical Data Coordinator Resume Examples & Samples

  • Ensure completion of supportive documentation for FIMs in medical record
  • Collect appropriate information from medical record and summarize on IRF-PAI
  • Ensure completion of admission PAI within four days of admission
  • Ensure completion of discharge PAI within five days of discharge
  • Check patient location roster and verify accuracy of IRF-PAI log
  • Ensure completion of all columns of IRF-PAI log with each discipline
  • Complete FIM competency
  • Assist in performing FIM competencies with other team members
18

Clinical Data Coordinator Resume Examples & Samples

  • Provide data analysis and performance improvement consulting for large-scale healthcare quality assessment and improvement projects
  • Review reports, identify trends in service and provider performance, initiate and design drill-down analysis, and support service-designated quality and performance improvement projects
  • Consults with managers, staff and physicians to support improvement activities and organizational initiatives
  • Coordinate both electronic and manual points of data collections, and assists in developing new data elements as needed
  • Educates and trains staff on data reporting requirements, relevant data definitions, and performance feedback
  • Minimum three years clinical or health related experience strongly preferred
  • Epic experience strongly desired
  • Experience with National Registry data submission preferred
  • Demonstrated ability to apply problem-solving skills in various job-related situations and to communicate effectively
19

Clinical Data Coordinator Resume Examples & Samples

  • Order, receive, manage, ship, remove/dispose, and perform regular audits of inventory (e.g., drugs, pesticides, active pharmaceutical ingredients, lab reagents, general laboratory and clinical supplies)
  • Import and export of research materials and supplies in coordination with domestic and international colleagues
  • Manage requests, labeling, shipment and disposition of clinical supplies in coordination with study personnel and study sites
  • Maintain (including archival as appropriate) documents related to inventory audits, import and export of materials and domestic and international shipments, and inventory reconciliation
  • Organize, maintain, and secure the Pharmacy areas with consideration of detailed documentation (e.g., monitoring, routine chart changes, and archival of temperature and humidity recorders, controlled temperature unit logbooks)
  • Maintain the electronic inventory database for cataloguing of inventory and facilitation of research shipment requests
  • Bachelor’s degree in a science or health related field plus 2 years of applicable experience preferred; a Master’s degree in a science or health related field and 1 or more years of applicable experience or a PHD or DVM may merit special consideration
  • Direct animal health clinical experience preferred
  • Experience with pesticides, pharmaceuticals, and API handling and packaging for shipment is preferred
  • Ability to handle changing work load and work effectively in teams
  • Excellent organizational skills with an ability to prioritize and manage multiple tasks
  • Familiarity with various computer programs, such as spread sheets, word processing, graphics/statistics, presentation packages and electronic communications
  • The incumbent must have a commitment to compliance, requiring an understanding of the regulatory requirements associated with management of research materials (GMP, GLP, FDA, EPA, and OSHA regulations)
20

Senior Clinical Data Coordinator Resume Examples & Samples

  • Perform routine data entry including first and second pass validation as required
  • Adhere to current data entry priorities using appropriate tools and resources
  • Add and resolve QC notes to data fields
  • Act as liaison for data management issues between SCHARP study teams and research sites
  • Attend assigned SCHARP study team meetings and conference calls
  • Assist in development of Case Report Forms for assigned studies
  • Manage study data for assigned studies
  • Assist in the maintenance of the study database including routine revisions or additions
  • Monitor study data to insure the quality and completeness of the data submitted by implementing quality control procedures as appropriate per CDMS
  • Generate QC reports for site review and correction as well as a variety of other reports as required
  • Evaluate study data for protocol compliance
  • Assist in production and review of Data Operations SOPs and WPGs
  • Assist Data Operations staff in resolving non-routine data entry issues
  • Perform additional tasks as appropriate and assigned
  • Bachelor’s degree or equivalent, preferably in a health-related or scientific discipline
  • 2+ years’ experience in the pharmaceutical/clinical research environment as Clinical Data Coordinator or equivalent role
  • EDC experience required. Working knowledge of Medidata Rave highly desirable. Demonstrated expertise in relevant clinical data management activities
  • Working knowledge of ICH/GCP guidelines and FDA regulations
  • Familiarity with all phases of clinical trials and ability to adapt to study requirements
  • Strong verbal and written communication skills. Ability to understand and follow instructions and guidelines; able to pick up new tasks quickly; willing to ask questions when a task is not fully clear
  • Ability to exercise independent judgment within generally defined practices and policies. Shows good judgment in interpreting guidelines and in when to seek support
  • Ability to work independently and to work efficiently under pressure
  • A strong team player with optimistic attitude
21

Clinical Data Coordinator Resume Examples & Samples

  • Previous experience in clinical trials
  • Detail oriented and ability to multi-task
  • Good communication, interpersonal and organizational skills
  • Quality patient care directly and indirectly
  • Basic proficiency in computer skills
  • Proficient in clinical data entry
  • Bachelor’s degree. Related experience can be substituted year for year to offset degree
  • Previous oncology experience
  • Exceptional database software skills
  • Research Certification
22

Clinical Data Coordinator Resume Examples & Samples

  • Two to five years previous experience with clinical research administration. Data management experience with Microsoft Excel, REDCap, CRIS, Access, or other electronic data capture systems
  • Experience with electronic medical records and working knowledge of medical terminology
  • Knowledge of medical terminology and clinical diagnoses
  • Experience with electronic health records, specifically Epic O2, Redcap, Medidata Rave, etc
  • Preferable background of health information management
  • The following certifications are preferred: CCRA, CCRC, or CCRP
23

Clinical Data Coordinator Resume Examples & Samples

  • 5 years of experience in clinical or a related field
  • 3 years of experience in data management and coordination with knowledge about database development, data quality principles, and statistical methodologies
  • Experience in research with knowledge of research principles, methodologies, and study design
  • Experience in the subspecialty of involvement
  • Collaborative Institutional Training Initiative (CITI) certification
  • Able to communicate knowledge of federal regulations and regulatory requirements regarding patient confidentiality
  • Self-directed and motivated to work independently toward short- and long-term goals
  • Ability to exercise independent judgment in doing medical summaries with strong analytical capabilities
  • Good communication, organization, and interpersonal skills
  • Good computer skills, including working knowledge of Microsoft Office (Word, Access, Excel, and PowerPoint) and basic statistics
  • Performs department-specific responsibilities related to ImproveCareNow Registry maintenance and data collection, including accurate/timely entry of clinical data, data entry into registry repository, adhering to data definitions, and ensuring data validation and integrity
  • Makes data available to physicians, physician assistants, nurse practitioners, registered nurses, and other team members
  • Provides reports on a regular basis and conducts team meetings to share data
  • Adheres to Health Insurance Portability and Accountability Act requirements regarding strict confidentiality of patient data, quality assurance indicators, and results of information collected
  • Maintains extensive records, including diseases and outcomes
  • May interact with other hospital staff and/or departments to request and collect data
  • Retrieves and tabulates necessary data regarding monthly patient activity, e.g., newly diagnosed, relapsed, progressions, and death
  • Supports and participates in the continuous assessment and improvement of quality data entry and analysis in collaboration with providers and members of the ImproveCareNow team
  • Works with team to identify quality improvement initiatives, implements improvement plans, monitors outcomes, and identifies opportunities for improvement
24

Clinical Data Coordinator Resume Examples & Samples

  • HS graduation and sufficient experience and demonstrated skills to successfully perform the assigned duties and responsibilities
  • Prior experience with various computer programs (Microsoft Office; internet-based databases) and using specialized software such as OnCore
  • Demonstrated knowledge and understanding of research, especially in the areas of biological sciences
  • Prior research experience or demonstrated ability to learn basic research methodologies and data reporting
  • Familiarity with, or have the ability to interpret and extract medical, oncologic, and scientific terminology
  • Demonstrated proficiency in medical terminology, human anatomy, and physiology
  • Data management experience in a medical setting, preferably with medical chart abstraction
  • Ability to relate effectively in person and via telephone and email with physicians, nurses, data managers, as well as medical records and information science departments
  • Attention to detail; strong interpersonal skills; excellent, effective verbal and written communication skills to coordinate with subjects, team members, other departments and outside institutions; and the ability to multi-task in a fast-paced environment while working with a diverse subject population
  • Ability to work well independently, complete projects in a timely manner, and prioritize multiple projects to ensure the completion of essential tasks by deadlines
  • Ability to work with a sensitive population of patients (oncology patients)
  • May need to travel between one or more campuses via UCSF shuttle
  • B.A. or B.S with a major in science or related
  • Prior analytical and writing skills in a science/research environment
  • Experience with FileMaker Pro and Microsoft Access
  • Experience with electronic data capture systems and clinical trial management systems such as OnCore and Oracle
  • Statistical background and training
  • Understanding of patient population to create rapport and a relationship, while also giving insight to what is realistic and appropriate for patient participation
  • Knowledge of UCSF and departmental policies for dealing with reimbursement, guidelines for research, confidentiality and HIPPA regulations, following the UCSF mission statement and purpose for research, and a clear understanding of policies and procedures on patient safety and confidentiality (electronic and hard copy medical records, patient charts, communication, etc.)
  • Knowledge of medical terminology, research policies and guidelines, guidelines for packing/shipping infectious substances, database building/analysis, and data management within some of the following: Access, Stata, SASS/ SPSS, and Teleform programming platforms
  • Knowledge of clinical research in breast oncology
  • Knowledge and experience in managing oncology clinical trials
  • Certificate in clinical research coordination (SoCRA, ACRP)
  • Membership in a clinical research professional society
  • Experience applying the following regulations and guidelines
25

Senior Clinical Data Coordinator Resume Examples & Samples

  • Provides cross coverage to other division on an as needed basis or at the supervisor's request
  • Ensures that electronic databases contain accurate, complete and up-to-date records of each patient participating in a clinical trial
  • Reviews source documents for completeness and registers patients to studies
  • Acts as Principal Investigator's representative as appropriate. This may include communicating with sponsors and their representatives, the IRB, and other medical personnel
  • Reviews medical record and prescreens patients for clinical trial eligibility
  • Prepares and assists for sponsor monitor site visits and ensures all supporting documentation records are adequate and available for the visit. Meets with monitor at least once during each monitor site visit and resolves all issues found during visit
  • Attends research meetings and conferences as required
  • Participates in staff meetings and in-service education
  • Lifts a minimum of 5 lbs., pushes and pulls a minimum of 10 lbs. and stands a minimum of 4 hours a day
  • Bachelor's degree in a health related field
  • Minimum of 5 years of Research Data Coordinator experience
  • Certified Clinical Research Professional
26

Clinical Data Coordinator Resume Examples & Samples

  • Utilizes the SAE reporting log to track the receipt, submission and acknowledgement of off-site SAEs per protocol
  • Prepare reports, including but not limited enrollment logs which assists with institutional statistical analysis
  • Ability to sit and concentrate at a computer workstation for a minimum of 4 hours at a single sitting
  • Bachelor's degree in Science (Chemistry, Biology, Nursing) or minimum of 3 years extensive experience in research that includes data abstracting, case report form completion and research regulatory reporting
27

Clinical Data Coordinator Resume Examples & Samples

  • Serve as a Data Operations Coordinator (DOC) for one protocol with less then 5 operations staff (excludes DE) or a
  • Serve in the role of back-up to a Data Operations Coordinator or Data Team Lead
  • Conduct data review
  • Write and resolve data clarifications
  • Lead database audit team
  • Develop and test databases and edit specifications
  • Meet objectives as assigned
  • Medical terminology exposure
  • Excellent organizational, communication, leadership and computer skills
  • Ability to exercise excellent attention to detail
  • Ability to act independently and with initiative required to resolving problems
  • Bachelor’s degree, or educational equivalence, in clinical, biological or mathematical sciences, or related field, or nursing
28

Clinical Data Coordinator Resume Examples & Samples

  • Run ancillary programs (e.g., diagnostics, special listings, reconciliation discrepancy listings) used to support the review of clinical trial data
  • Generate, resolve and track queries to address problematic data identified during data review activities and apply proper modification / correction to the database
  • Apply quality control procedures and checks to ensure data quality standards (client and Covance) are achieved
  • Interact with the dictionary coding and maintenance group to ensure appropriate process set-up and application
  • Assist with the aggregate review of clinical data by patient, site, and/or project to identify data trends (patient safety, compliance, etc.), and/or data inconsistencies that require further investigation
  • Assist in the development and testing of data management system edit / data validation checks (diagnostics) and special listings / procedures used as tools for the data review and discrepancy management activities
29

Senior Clinical Data Coordinator Resume Examples & Samples

  • Development of database build specifications
  • Development of data validation specifications
  • Test data creation & UAT
  • Assist with the validation of edit check programs
  • Study status tracking
  • Review of data listings
  • Conduct SAE & third party data reconciliations
  • Maintaining Clinical Study Documents and archiving as appropriate
  • Represent Data Management at internal / external meetings as appropriate
  • Perform early and final database QC activities
  • Database lock activities