625 Mds Consultant jobs in the United States
Regional MDS Consultant (RN)
Posted 13 days ago
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Job Description
We rely on and trust our Regional MDS Consultant to provide extensive training, analysis, direction, action plan/resolution and consultation to the facilities, district and regional teams within his/her area of specialty.Why Work For Us? Competitive PayExcellent health benefits packages Career advancement opportunitiesEducation reimbursement program of up to $7,500 per year Benefits & Conditions:No waiting period for enrollmentThree health plan optionsDelta DentalVSP VisionFree Basic Life InsuranceDisability, Critical Illness, Accident & Legal Coverage401(k) Retirement PlanEmployee Assistance ProgramResponsibilities:Validates compliance with federal and state regulations as well as Company policy and procedures regarding state case mix/Medicare payment systems, RAI process and operations Provides direct consultation, training and support related to the RAI Process. Medicare and state case mix payment system for assigned area.Monitors, consults, and makes effective recommendations for changes and modifications to existing facility processes, systems, policies, and practices which will assure efficient, effective and compliant state Medicaid/Medicare payment performance and RAI process completion.Responsible for training Registered Nurse Assessment Coordinator (RNAC) on accuracy and systems related to RUG mix, RAI process and Grouper calculation.Responsible for effective action plan resolution in areas of RAI process case-mix/Medicare system and action plans to necessary parties.Serves as a liaison between state and organization related to the state case-mix process, including electronic submission and state MDS requirements related to state payments.Qualifications:RN or completion of a Bachelor's Degree in a health care or related fieldFive to seven years of clinical experience in a long-term care setting, which includes supervisory, administrative, or consultative capacitiesCurrent knowledge of state case mix and Medicare payment systemsCapable of maintaining regular attendanceMust be able to work favorably across departments#BYHCIND
Regional MDS Consultant, Regional Clinical Reimbursement Specialist
Posted today
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Job Description
We are searching for a Regional MDS Consultant/Clinical Reimbursment Specialist to join our community that is employee focused, a team builder, and excited about the opportunity to assist in building a facility culture.
Regional Experience preferred, but not required.
Benefits
- Pay rate: Competitive salary
- Access to online learning 24/7: . Use it for free to help satisfy your state specific licensure requirements.
- Health insurance for the entire family
- 401k with a match!
- Serve as the primary resource person to facility MDS Coordinators related to HCS's processing of the MDS.
- Conduct orientation sessions to all employees involved in the MDS process.
- Provide ongoing education for employees involved in HCS processing as deemed necessary and assigned by supervisor.
- Maintain current working knowledge of MDS and ensure regulatory change are applied to the program and functional.
- List and track support calls to assist in training and staff development.
- Advise supervisor and HCS liaison of support items that require program adaptations or enhancements.
- Develop training materials and distribute to facility staff as needed.
- Update the MDS User Manual as necessary.
- Travel to facilities as needed to evaluate facility production and train facility staff.
- Create weekly update of current HCS MDS issues being addressed, fix-it procedural guides and other information and issue to the facilities.
- Review facility processing and advise Administrator of abnormal trends.
- Prepare and submit reports on facility operations, as required.
- Attend and/or conduct meetings, as required, to carry out responsibilities.
- Ensure adequate preparation for, and participate in, regulatory compliance surveys.
- Must stay in compliance with all state, federal, and government agencies.
- Demonstrate respect and compassion in every interaction.
- Conduct oneself with the highest degree of honesty and integrity in every interaction.
- Demonstrate a passion for caring as evidenced by interaction with co-workers, residents, families, and visitors.
- Perform other duties as assigned.
- Must possess a current, unencumbered, active state license to practice as an RN.
- Experience in Skilled Nursing/Rehabilitation facilities.
- Must have extensive working knowledge in the following: the MDS completion process, the HCS MDS Program and it functionality in the long term care environment.
- Preferred experience in a multi-site, regional capacity.
- Two (2)-Three (3) years of experience as a MDS Coordinator.
- RAC-CT or RNAC preferred.
- Leadership and supervisory experience preferred.
- You must be qualified, compassionate, and dedicated to a job well done.
We strive to create an environment where people feel safe, heard, and understood. Our leadership teams embrace our "people first" philosophy
We're an equal opportunity employer. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or disability status.
Regional MDS Nurse Consultant
Posted today
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Job Description
Job description
We are looking for a friendly, reliable and long-term candidate to provide clinical leadership in the development, implementation, coordination and evaluation of MDS services across multiple facilities. The Regional MDS Nurse Consultant will support quality care and fiscal responsibility through comprehensive MDS training and support services for assigned region. You will be responsible for the training and program review of MDS Services in accordance with Federal, State and Local laws and governing entity regulations.
Regional MDS Nurse Consultant role will cover facilities in Georgia.
Qualifications
- Currently licensed as RN /LPN in the state of Georgia
- Associate or bachelor’s degree from an accredited nursing school required.
- Minimum of five (5) years in long-term care required,
- Minimum of five (5) years working as an MDS Nurse in long-term or acute health care
- At least two (2) years of multi-facility, regional MDS experience preferred.
RESPONSIBILITIES
- Consults with and provides technical assistance to the MDS Coordinators through visits and the interpretation or clarification of policies and regulations.
- Trains new MDS Coordinators in conducting resident assessments, developing plans of care, evaluating residents’ responses to interventions and documenting clinical records.
- Trains new MDS Coordinators on the RAI manual and all applicable deadlines for resident assessments and completion of Minimum Data Sets (MDSs).
- Observes MDS and related practices for compliance with standards and regulations.
- Regularly inspects the facility and nursing practices for compliance with standards of nursing practice and federal, state and local regulations
- May be required to assume the role of interim MDS Coordinator, as needed.
- Ability to train facility MDS regarding company best practices including consistent coordination with other members of Compliance Team i.e. DON, BOM, Medical Records, and Therapy to ensure compliant billing.
- Leads the facility management staff and consultants in developing and working from a business plan that focuses on all aspects of facility operations, including clinical management.
- Responsible for developing and implementing appropriate metrics and benchmarks for company's quality of care, against which performance is evaluated.
- Regularly advises and directs Clinical Support Team, Director of Nursing to maximize resident satisfaction and wellbeing.
- Develops and utilizes a standardized process to evaluate and evolve practice to decrease variability and improve the care and safety of patients.
- Responsible for developing, implementing and monitoring quality management policies and procedures for quality data collection and reporting on QM measures.
- Conduct ongoing assessments of the existing eligibility and referrals, case management, disease management systems, and Quality Management programs within each clinical. Provide objective evaluation and recommendations for those systems.
- Review existing clinic information system capabilities for the tracking and monitoring of quality indicators. Make the necessary adaptations for standardized reporting across all centers
- Resident Assessment Instrument (RAI) guidelines are followed in the assigned region with focus on resident care and mixing financial reimbursement through the MDS process. Responsible for ensuring accurate and timely completion of resident assessments, in accordance with Medicare, Medicaid, OBRA and other payer program requirements.
- Ensure regulatory compliance to all federal, state and local regulations and laws relating to nursing home administration; guide facilities to operate within established company policies and practices
- Ensures each facility maintains building and grounds to appropriate standards and that equipment and work areas are clean, safe and orderly, and any hazardous conditions are addressed; ensure that Universal Precaution and Infection Control, Isolation, Fire Safety and Sanitation practices and procedures are followed.
- Helps the Administrator prepare staff for inspection surveys, instructing staff on matters of conduct and disclosure, being interviewed by inspectors, immediate corrections of problems noted by surveyors, etc. Reviews and reinforces important standards previously cited.
- Participates in the preparation of the Plan of Correction response to an inspection survey and implements any follow up QA required for any nursing allegations.
- Provides 24-hour “on call” service to the nursing center in case of emergency.
- Assures that an adequate orientation and in-service training program is provided for MDS personnel.
- Other duties, responsibilities and activities may change or assigned at any time with or without notice.
EQUAL OPPORTUNITY EMPLOYER
Regional MDS Coordinator/Consultant
Posted today
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Job Description
Location: Ashville, North Carolina - West Region
Job Type: Full-Time
Travel Requirement: Extensive, including overnight stays and extended periods of time
About Avardis and Who We Are:
OUR VISION We strive to be the leading provider of compassionate, comprehensive care that supports the physical, mental, and emotional well-being of patients, while also promoting respect and autonomy. Our goal is to create an environment where patients thrive, not just survive - where every aspect of their well-being is nurtured, from health and safety to social connections and quality of life.
Innovative Solutions for Better Health As part of our commitment to excellence, Avardis leverages the latest in healthcare technology to provide better outcomes for older adults. From telemedicine services and remote health monitoring to advanced diagnostic tools and customized wellness programs, we use innovation to make patient care accessible, efficient, and effective.
We also embrace new treatments, therapies, and approaches that can improve quality of life, whether it's through pain management, physical rehabilitation, or mental health support. By staying at the forefront of healthcare trends and continuously evolving our services, we ensure that patients receive the best possible care.
About the Role:
We are seeking a Regional Director of MDS to oversee the clinical reimbursement process and ensure compliance across multiple skilled nursing facilities. If you are passionate about resident care, regulatory compliance, and leadership development, this role is for you!
Major Responsibilities:
- Lead & Inspire - Educate, mentor, and develop MDS Coordinators across multiple locations.
- Strategic Role - Oversee MDS compliance and reimbursement strategies across facilities.
- Make an Impact - Ensure high-quality resident assessments and care planning.
- Provide ongoing education, mentorship, and leadership development to facility MDS Coordinators.
- Travel to various skilled nursing facilities to provide hands-on support and guidance.
- Oversee the coordination and completion of the Resident Assessment Instrument (MDS, CAA's, and Care Plan) in compliance with federal and state regulations.
- Monitor and document the management of Medicare and Managed Care residents in collaboration with facility teams.
- Ensure accurate assessments and documentation to support proper reimbursement and quality care.
- Develop and implement innovative strategies to improve MDS processes and optimize clinical
Minimum Qualifications:
- Licensure: Current, active, and unencumbered RN license.
- Experience:
- Skilled Nursing/Rehabilitation facility experience required.
- Multi-site, regional experience preferred.
- Two (2)-three (3) years of experience as an MDS Coordinator.
- Certifications: RAC-CT or RNAC preferred.
- Leadership: Supervisory and leadership experience preferred.
Why Join Us?
- Pay rate: Competitive salary and bonus structure may apply, along with holiday pay and unlimited Work Life Balance (WLB) program.
- Access to online learning 24/7: Our Learning Management System offers over 1,500 courses for senior care, health and human services industry. Use it for free to help satisfy your state specific licensure requirements. Data base includes MS Office and Leadership/Supervisory content. Available via computer or mobile, and many courses are offered in alternative languages.
- Advocacy and Community Impact : At Avardis, we are not just focused on the well-being of our patients - we are committed to making a positive impact on the communities we serve. We partner with local organizations, host educational events, and advocate for policies that improve the health and lives of older adults everywhere.
Join us in creating a future where every patient is empowered to live their best life, with the support and care they deserve.
We're an equal opportunity employer. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or disability status.
Job Posted by ApplicantPro
Clinical Data Assistant
Posted 18 days ago
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Job Description
We are seeking a full time, detail-oriented and motivated Clinical Data Assistant to support our Clinical Data team. This entry-level position is ideal for someone interested in beginning a career in clinical research or quality assurance (QA). The primary responsibility of this role is to upload study-related documents to the eSource platform while developing a strong foundation in clinical research practices and data quality management.In addition to core duties, this individual will be expected to maintain a flexible, proactive mindset, ready to assist with various administrative, operational, and data tasks as needed throughout the organization.RequirementsResponsibilities:•Scan/Upload and organize clinical study documents into the eSource system accurately and efficiently•Learn and apply basic principles of clinical research, data management, and quality assurance•Support the Clinical Data Coordinators in document review and preparation•Assist with version control and tracking of study documents and source materials•Shadow team members to gain exposure to data entry processes, CRFs, and data cleaning activities•Help identify and resolve minor document discrepancies under supervision•Support general administrative duties interdepartmentally and contribute to cross-functional tasks as needed•Remain adaptable and willing to assist with ad hoc projects or operational needs across departments•Identifies potential study issues/risks and recommends solutions•Supports the Data Entry Manager in executing the data management plan•Designs and modifies source documents, extracts, and monitors the trial data to identify issues•Works with clinical research team members to review data and highlight inconsistencies•Assists clinical teams to facilitate the clinical team review of system and/or specifications•Other duties as assignedExperience and Skills:•Strong attention to detail and organizational skills•Ability to learn quickly and follow documented procedures•Familiarity with basic Microsoft Office applications (Word, Excel, Outlook)•Willingness to ask questions and learn on the job•A collaborative and helpful attitude•Comfort with handling confidential documents with discretion•Proactive and open to performing a variety of tasks to support team success•Excellent written, verbal and interpersonal communication skills•Proficient typing and data entry skills•Ability to manage small projects personally and work independently•Time management skills•Organizational skills•Detail oriented with the ability to perform at a high level of accuracy•Demonstrates strong analytical and problem solving skills•Self motivatedEducation and Experience:•High school diploma or GED is required•No prior experience required, but interest or background in healthcare, science, or administrative support is a plus•Previous exposure to a clinical, healthcare, or office setting is helpful but not necessarySalary Description $18.00 - $21.00 (hourly)
Clinical Data Analyst

Posted today
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Job Description
Location: Chicago, Illinois
Business Unit: Rush Medical Center
Hospital: Rush University Medical Center
Department: Research Computing
**Work Type:** Full Time (Total FTE between 0.9 and 1.0)
**Shift:** Shift 1
**Work Schedule:** 8 Hr (7:00:00 AM - 3:00:00 PM)
Rush offers exceptional rewards and benefits learn more at our Rush benefits page ( Range:** $34.61 - $51.57 per hour
Rush salaries are determined by many factors including, but not limited to, education, job-related experience and skills, as well as internal equity and industry specific market data. The pay range for each role reflects Rush's anticipated wage or salary reasonably expected to be offered for the position. Offers may vary depending on the circumstances of each case.
**Summary:**
The Analyst will support the research, clinical, quality improvement, and business data analysis needs of Rush University Medical Center. The Analyst will assist clinical faculty and Principal Investigators to identify and gather necessary data that span operational through research needs and will build databases to permit queries. The analyst will have a direct reporting relationship to the Knowledge Management Team, Medical Director, and Chief Analytics Officer, who are the subject matter experts in data access and research data requests. Exemplifies the Rush mission, vision and values and acts in accordance with Rush policies and procedures.
**Other information:**
**Required Job Qualifications:**
- Master's degree in information science, computer science, epidemiology, biostatistics, or equivalent technical experience.
- Strong analytic, issue resolution, and facilitation skills.
- Demonstrated proficiency writing SQL stored procedures or queries.
- Able to present complex information in an understandable and compelling manner.
- Able to prioritize and multi-task to manage expectations of multiple stakeholders.
- Able to deliver high quality, timely work product with significant autonomy.
- Effectively adapts to rapid changes in project or data requirements and changing directions.
- Strong written and verbal communication.
- Effective interpersonal and teamwork skills.
- Expertise with data and analytics tools.
- Experience querying and analyzing data with SQL programming language or equivalent tools.
**Preferred Job Qualifications:**
- At least three years of experience in statistical software (e.g. SAS or R), with data science experience.
- Some experience in the health care setting.
- Familiarity with healthcare industry or healthcare information systems.
- Experience with Epic.
- Experience with financial /claims data.
**Responsibilities:**
- Gather business/data requirements from clinical faculty and Principal Investigators and collaborate on the best way to design studies or to build study cohorts based on the Analyst's knowledge of available systems. Acts as interface between clinical experts and IT to determine feasibility, timelines, and cost of date requests.
- Uses third party software tools and research data warehouse in development of queries and visualizations. Creates research data marts using the enterprise IT architecture.
- Serves as representative for the KM Team on committees and initiatives that involve multi-site studies to facilitate IT and research informatics collaborations.
- Participates in analytics-based projects that leverage data collected from electronic medical records to measure and predict patient outcomes.
- Works with statisticians and mathematicians to design predictive models using statistical and machine learning methods that will predict patient outcomes.
- Develops analytic data sets for research and operations and uses statistical software (SAS or R) to analyze data sets as requested by departmental faculty.
- Produces reports that facilitate evidence-based clinical and financial decisions.
- Works with CRIO/CMIO/Knowledge Management team to develop new data queries and toolsets.
- Member of the IT business intelligence/knowledge management team at Rush. Maintains peer relationship and collaborative knowledge exchange with IT counterparts.
Rush is an equal opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, and other legally protected characteristics.
**Position** Clinical Data Analyst
**Location** US:IL:Chicago
**Req ID** 19830
Clinical Data Reviewer

Posted today
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Job Description
**What you will be doing:**
+ Serve as a Clinical Data Reviewer and identify any errors in data by performing data review that require further clarification with the study sites
+ Perform ongoing review of clinical/medical aspects of assigned patient data and documents
+ Communicates any data training needs for CRAs, sites, etc
+ Conduct in-stream data trend analysis in support of data quality and integrity (includes protocol compliance and targeted review of patient data)
+ Provide clinical data Project Management and viewed as an expert in data clinical/medical review and cleaning.
+ Ensure data quality focus to audit readiness with Clinical Compliance and Systems Validation
+ May assist in review and contribute to data capture requirements guidance in line with protocol and reporting requirements.
+ May be closely involved in data review and identification of readiness for clinical narratives for CSRs
+ May participate in clinical data review meetings such as:
o Protocol Deviation review
o Data Review and Quality Team (DRQT)
o Statistical Review of Clinical Data (SRCD)
o Safety Monitoring Team (SMT) review
o Slide preparation of top-line results
**You are:**
+ Educational scientific background such as MD, PharmD, PhD, Nursing degree, MS
+ ≥ 5 years of pharmaceutical clinical/medical data review experience is required, including clinical crosscheck experience. 8+ years is preferrable
+ Experience with Solid Tumor Oncology
+ Excellent verbal and writing communication in English, organization and tracking skills. Strong operational skills and demonstrated ability to meet timelines.
+ Experience in coding review
+ Query writing training
+ Strong clinical database navigation skills
+ Strong MS excel, project management
+ Knowledge of Good Clinical Practice; comprehensive knowledge of clinical trial design; understanding of the overall drug development process
+ Must work East coast hours
**What ICON can offer you:**
Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
+ Various annual leave entitlements
+ A range of health insurance offerings to suit you and your family's needs
+ Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead
+ Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family's well-being
+ Life assurance
+ Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others
Visit our careers website to read more about the benefits of working at ICON: ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.
in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.
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Clinical Data Manager

Posted 3 days ago
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Job Description
**Clinical Data Manager**
**Working at Abbott**
At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You'll also have access to:
+ Career development with an international company where you can grow the career you dream of.
+ Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.
+ An excellent retirement savings plan with a high employer contribution
+ Tuition reimbursement, the Freedom 2 Save ( student debt program, and FreeU ( education benefit - an affordable and convenient path to getting a bachelor's degree.
+ A company recognized as a great place to work in dozens of countries worldwide and named one of the most admired companies in the world by Fortune.
+ A company that is recognized as one of the best big companies to work for as well as the best place to work for diversity, working mothers, female executives, and scientists.
**The Opportunity**
The Clinical Data Manager is responsible for performing data management tasks within defined established processes throughout the life cycle of the study including startup, conduct and reporting phases. The Clinical Data Manager is also responsible for the development, maintenance and training of peers in the applicable processes. This role is critical to the successful collection, reporting and analysis of clinical trial data as well as the mentorship of junior team members.
This position will be based out of our Abbott Diabetes Care in Alameda, CA and the individual will be expected to be onsite Monday-Friday.
**What You'll Work On**
+ Assist in translation of clinical study requirements into trial Casebook.
+ Develop and maintain Data Management Plans (DMPs) for clinical trials.
+ Develop edit check specifications for the automated cleaning of data management practices and procedures (SOPs, Work Instructions), including identifying and recommending solutions for technology issues.
+ Conduct user acceptance testing of clinical study databases, reports, study notifications and database customizations
+ Develop study specific data listings and ensure data accuracy and integrity
+ Identify and resolve data discrepancies and inconsistencies.
+ Identify opportunities for improvement and proposed solutions, develop procedures and train to new processes.
+ Mentor junior team members in the roles and responsibilities of the Clinical Data Management Analyst.
**Required Qualifications**
+ B.S. in Computer Science, Life Sciences or Technical Field.
+ Equivalent combination of education and work experience will be considered.
+ Minimum 5 years in clinical or medical or research setting.
**Preferred Qualifications**
+ Expert in data collection best practices for clinical trials.
+ Expert knowledge of global clinical operations.
+ Experience utilizing electronic data capture systems (EDC) and eTMF systems.
+ Knowledge of industry-standard data analysis and reporting software, such as SAS and SQL.
+ Intermediate to advanced therapy specific knowledge of anatomy, physiology, pathophysiology, therapy and device.
+ Intermediate to advanced medical knowledge related to common medical histories, medical terminology, diagnostics (imaging, laboratory), and medications (class, dose, route).
+ Excellent attention to detail with problem-solving and analytical skills.
+ Certified Clinical Data Manager (CCDM) or equivalent.
Apply Now ( more about our health and wellness benefits, which provide the security to help you and your family live full lives:** ( your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.
Connect with us at , on Facebook at , and on Twitter @AbbottNews.
**Divisional Information**
Medical Devices
General Medical Devices:
Our medical devices help more than 10,000 people have healthier hearts, improve quality of life for thousands of people living with chronic pain and movement disorders, and liberate more than 500,000 people with diabetes from routine fingersticks.
Diabetes
We're focused on helping people with diabetes manage their health with life-changing products that provide accurate data to drive better-informed decisions. We're revolutionizing the way people monitor their glucose levels with our new sensing technology.
The base pay for this position is $86,700.00 - $173,300.00. In specific locations, the pay range may vary from the range posted.
An Equal Opportunity Employer
Abbot welcomes and encourages diversity in our workforce.
We provide reasonable accommodation to qualified individuals with disabilities.
To request accommodation, please call or email
Clinical Data Manager

Posted 3 days ago
Job Viewed
Job Description
**Clinical Data Manager**
**Working at Abbott**
At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You'll also have access to:
+ Career development with an international company where you can grow the career you dream of.
+ Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.
+ An excellent retirement savings plan with a high employer contribution
+ Tuition reimbursement, the Freedom 2 Save ( student debt program, and FreeU ( education benefit - an affordable and convenient path to getting a bachelor's degree.
+ A company recognized as a great place to work in dozens of countries worldwide and named one of the most admired companies in the world by Fortune.
+ A company that is recognized as one of the best big companies to work for as well as the best place to work for diversity, working mothers, female executives, and scientists.
**The Opportunity**
The Clinical Data Manager is responsible for performing data management tasks within defined established processes throughout the life cycle of the study including startup, conduct and reporting phases. The Clinical Data Manager is also responsible for the development, maintenance and training of peers in the applicable processes. This role is critical to the successful collection, reporting and analysis of clinical trial data as well as the mentorship of junior team members.
This position will be based out of our Abbott Diabetes Care in Alameda, CA and the individual will be expected to be onsite Monday-Friday.
**What You'll Work On**
+ Assist in translation of clinical study requirements into trial Casebook.
+ Develop and maintain Data Management Plans (DMPs) for clinical trials.
+ Develop edit check specifications for the automated cleaning of data management practices and procedures (SOPs, Work Instructions), including identifying and recommending solutions for technology issues.
+ Conduct user acceptance testing of clinical study databases, reports, study notifications and database customizations
+ Develop study specific data listings and ensure data accuracy and integrity
+ Identify and resolve data discrepancies and inconsistencies.
+ Identify opportunities for improvement and proposed solutions, develop procedures and train to new processes.
+ Mentor junior team members in the roles and responsibilities of the Clinical Data Management Analyst.
**Required Qualifications**
+ B.S. in Computer Science, Life Sciences or Technical Field.
+ Equivalent combination of education and work experience will be considered.
+ Minimum 5 years in clinical or medical or research setting.
**Preferred Qualifications**
+ Expert in data collection best practices for clinical trials.
+ Expert knowledge of global clinical operations.
+ Experience utilizing electronic data capture systems (EDC) and eTMF systems.
+ Knowledge of industry-standard data analysis and reporting software, such as SAS and SQL.
+ Intermediate to advanced therapy specific knowledge of anatomy, physiology, pathophysiology, therapy and device.
+ Intermediate to advanced medical knowledge related to common medical histories, medical terminology, diagnostics (imaging, laboratory), and medications (class, dose, route).
+ Excellent attention to detail with problem-solving and analytical skills.
+ Certified Clinical Data Manager (CCDM) or equivalent.
Apply Now ( more about our health and wellness benefits, which provide the security to help you and your family live full lives:** ( your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.
Connect with us at , on Facebook at , and on Twitter @AbbottNews.
**Divisional Information**
Medical Devices
General Medical Devices:
Our medical devices help more than 10,000 people have healthier hearts, improve quality of life for thousands of people living with chronic pain and movement disorders, and liberate more than 500,000 people with diabetes from routine fingersticks.
Diabetes
We're focused on helping people with diabetes manage their health with life-changing products that provide accurate data to drive better-informed decisions. We're revolutionizing the way people monitor their glucose levels with our new sensing technology.
The base pay for this position is $86,700.00 - $173,300.00. In specific locations, the pay range may vary from the range posted.
An Equal Opportunity Employer
Abbot welcomes and encourages diversity in our workforce.
We provide reasonable accommodation to qualified individuals with disabilities.
To request accommodation, please call or email
Clinical Data Analyst
Posted 1 day ago
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Job Description
**Job Summary/Purpuse**
The Clinical Data Analyst works with management and staff to define problems, devise solutions, perform work flow analysis, quality control and problem and change management. The position analyzes, reports, presents and encourages the use of data to monitor and improve care and for designing related processes and systems. The Clinical Analyst supports advanced clinical quality inquiry leading to ad hoc report generation and further investigative analysis, often leading to new clinically relevant information used to improve quality, safety, service and growth. The position facilitates the establishment of a data driven culture in the clinical quality and operational areas
**Key Responsibilities**
+ Responsible for collecting, tracking and reporting quality measures /indicators across the system.
+ Produces reports that are timely and accurate.
+ Seeks opportunities to automate or otherwise improve the accuracy and efficiency of data collection and reporting.
+ Able to speak about business issues outside of data management, including clinical finance,clinical operations, clinical quality metrics, and process improvements to insure proper focus and results against performance metrics
+ Provide project leadership and ongoing support of multiple clinical systems
+ Provide collection and distribution of data and other documents to meet regulatory and system benchmarking requirements
+ Perform project support, data analysis and synthesis of clinical and administrative data from multiple sources into meaningful summary reports and presentations
+ Attend multi-disciplinary team meetings and review data for opportunities for improvement
+ Able to identify major trends in data collection, prepare graphs and measurement tools and report variances in data
+ Demonstrate ability to merge clinical and financial data, database creation and management
**Qualifications**
**Required Education**
Bachelor's degree required.
**Required Licenses/Certifications**
n/a
**Required Minimum Knowledge, Skills, and abilities**
Minimum of three years of experience conducting and reporting complex data analyses using statistical methods, preferably in an applied clinical environment. Business management experience in addition to experience in Cerner, Epic, Meditech, Allscripts, Premier helpful. Working knowledge of National Quality Forum (NQF), Agency for Healthcare Research and Quality (AHRQ), Institutes for Healthcare Improvement (IHI) safety indicators, serious reporting events, safe medical practices, and Centers for Medicare and Medicaid Services (CMS) quality measures helpful.
**Preferred Qualifications**
Minimum of 3 years experience in the discipline preferred.
**Overview**
**Your time at work should be fulfilling.** Rewarding. Inspiring. That's what you'll find when you join one of our non-profit CHI facilities across the nation. You'll find challenging, rewarding work every day alongside people who have as much compassion as you. Join us and together we'll create healthier, stronger communities.
**Pay Range**
$24.27 - $34.64 /hour
We are an equal opportunity/affirmative action employer.