Clinical Data Coordinator Resume Samples

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L Douglas

Lazaro

Douglas

5888 Pablo Hill

San Francisco

+1 (555) 511 3535

5888 Pablo Hill

San Francisco

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

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

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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

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

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

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

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

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

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

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

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

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

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

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)

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

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

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

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

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

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

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)

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

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

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

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

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

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

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

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

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

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