Develop CRF specifications from the clinical study protocol and coordinate the review/feedback from ... Perform medical coding of medical terms relative to each other in order to ensure medical logic and ...
Develop CRF specifications from the clinical study protocol and coordinate the review/feedback from ... Perform medical coding of medical terms relative to each other in order to ensure medical logic and ...
Develop CRF specifications from the clinical study protocol and coordinate the review/feedback from ... Perform medical coding of medical terms relative to each other in order to ensure medical logic and ...
Develop CRF specifications from the clinical study protocol and coordinate the review/feedback from ... Perform medical coding of medical terms relative to each other in order to ensure medical logic and ...
We welcome candidates from all backgrounds to join our team , fostering a strong sense of belonging ... Oversee and as needed, directly support coding review for adverse events, medical history and ...
We welcome candidates from all backgrounds to join our team , fostering a strong sense of belonging ... Oversee and as needed, directly support coding review for adverse events, medical history and ...
Coding Guidelines * Annotated CRFs * Edit Check Specifications * Attend study-specific team ... to close on 60 days from when it is posted or sooner if the position is filled or closed.
Coding Guidelines * Annotated CRFs * Edit Check Specifications * Attend study-specific team ... to close on 60 days from when it is posted or sooner if the position is filled or closed.
We welcome candidates from all backgrounds to join our team , fostering a strong sense of belonging ... Oversee and as needed, directly support coding review for adverse events, medical history and ...
We welcome candidates from all backgrounds to join our team , fostering a strong sense of belonging ... Oversee and as needed, directly support coding review for adverse events, medical history and ...
Clinical Data Manager
Sunnyvale, CA · On-site
$70 - $75/hr
Support clinical data review requirements from Lead data manager. * Create customise data review listings for study per specifications from lead data manager. * Provide clinical data management ...
Quick apply
Clinical Data Manager
Sunnyvale, CA · On-site
$70 - $75/hr
Support clinical data review requirements from Lead data manager. * Create customise data review listings for study per specifications from lead data manager. * Provide clinical data management ...
1) Lead clinical data manager with 3 -5 years of Sponsor or CRO or Academic experience 2) Project ... The selected candidate will manage biomarker data in various stages, from planning, to set-up ...
1) Lead clinical data manager with 3 -5 years of Sponsor or CRO or Academic experience 2) Project ... The selected candidate will manage biomarker data in various stages, from planning, to set-up ...
The Clinical Data Associate is required to represent the clinical data sciences function and ... Articulating the flow of data (structure and format) from study start-up to analysis and applying ...
The Clinical Data Associate is required to represent the clinical data sciences function and ... Articulating the flow of data (structure and format) from study start-up to analysis and applying ...
Clinical Data Associate
Indianapolis, IN · On-site
The Clinical Data Associate is required to represent the clinical data sciences function and ... Articulating the flow of data (structure and format) from study start-up to analysis and applying ...
Clinical Data Associate
Indianapolis, IN · On-site
The Clinical Data Associate is required to represent the clinical data sciences function and ... Articulating the flow of data (structure and format) from study start-up to analysis and applying ...
The Senior Clinical Data Manager is responsible for all aspects of the data management process from ... Coordinates the internal medical coding review. * Performs ad hoc and scheduled data listing review ...
The Senior Clinical Data Manager is responsible for all aspects of the data management process from ... Coordinates the internal medical coding review. * Performs ad hoc and scheduled data listing review ...
1) Lead clinical data manager with 3 -5 years of Sponsor or CRO or Academic experience 2) Project ... The selected candidate will manage biomarker data in various stages, from planning, to set-up ...
1) Lead clinical data manager with 3 -5 years of Sponsor or CRO or Academic experience 2) Project ... The selected candidate will manage biomarker data in various stages, from planning, to set-up ...
Senior Clinical Data Manager
Redwood City, CA · On-site
The Senior Clinical Data Manager is responsible for all aspects of the data management process from ... Coordinates the internal medical coding review. * Performs ad hoc and scheduled data listing review ...
Senior Clinical Data Manager
Redwood City, CA · On-site
The Senior Clinical Data Manager is responsible for all aspects of the data management process from ... Coordinates the internal medical coding review. * Performs ad hoc and scheduled data listing review ...
Senior Clinical Data Manager
Culver City, CA · On-site +1
Coding Guidelines * Annotated CRFs * Edit Check Specifications * Attend study-specific team ... to close on 60 days from when it is posted or sooner if the position is filled or closed.
Senior Clinical Data Manager
Culver City, CA · On-site +1
Coding Guidelines * Annotated CRFs * Edit Check Specifications * Attend study-specific team ... to close on 60 days from when it is posted or sooner if the position is filled or closed.
Clinical Data Manager
Sunnyvale, CA · On-site
Lead end-to-end clinical data management activities from protocol review through database lock and study closeout * Design and oversee data collection strategy, including CRF/eCRF development ...
Clinical Data Manager
Sunnyvale, CA · On-site
Lead end-to-end clinical data management activities from protocol review through database lock and study closeout * Design and oversee data collection strategy, including CRF/eCRF development ...
... Code Administrative Patient Sensitive Job Code? Yes Standard Hours per Week 40 Full Time or ... Comments This position is intended to be focused on study level activities with oversight from the ...
... Code Administrative Patient Sensitive Job Code? Yes Standard Hours per Week 40 Full Time or ... Comments This position is intended to be focused on study level activities with oversight from the ...
Lead Clinical Data Manager (Remote)
Tampa, FL · Remote
$68K - $217K/yr
This is a remote/WFH position with all necessary equipment provided. What You'll Do * Lead data management for complex, global clinical trials from study setup to database lock. * Serve as the main ...
Lead Clinical Data Manager (Remote)
Tampa, FL · Remote
$68K - $217K/yr
This is a remote/WFH position with all necessary equipment provided. What You'll Do * Lead data management for complex, global clinical trials from study setup to database lock. * Serve as the main ...
Lead Clinical Data Manager (Remote)
New York, NY · Remote
$68K - $217K/yr
This is a remote/WFH position with all necessary equipment provided. What You'll Do * Lead data management for complex, global clinical trials from study setup to database lock. * Serve as the main ...
Lead Clinical Data Manager (Remote)
New York, NY · Remote
$68K - $217K/yr
This is a remote/WFH position with all necessary equipment provided. What You'll Do * Lead data management for complex, global clinical trials from study setup to database lock. * Serve as the main ...
Lead Clinical Data Manager (Remote)
Dallas, TX · Remote
$68K - $217K/yr
This is a remote/WFH position with all necessary equipment provided. What You'll Do * Lead data management for complex, global clinical trials from study setup to database lock. * Serve as the main ...
Lead Clinical Data Manager (Remote)
Dallas, TX · Remote
$68K - $217K/yr
This is a remote/WFH position with all necessary equipment provided. What You'll Do * Lead data management for complex, global clinical trials from study setup to database lock. * Serve as the main ...
The selected candidate will manage biomarker data in various stages, from planning, to set-up ... Works collaboratively with Biomarker Clinical Operations team members, Biomarker Scientists ...
The selected candidate will manage biomarker data in various stages, from planning, to set-up ... Works collaboratively with Biomarker Clinical Operations team members, Biomarker Scientists ...
Lead Clinical Data Manager (Remote)
Atlanta, GA · Remote
$68K - $217K/yr
This is a remote/WFH position with all necessary equipment provided. What You'll Do * Lead data management for complex, global clinical trials from study setup to database lock. * Serve as the main ...
Lead Clinical Data Manager (Remote)
Atlanta, GA · Remote
$68K - $217K/yr
This is a remote/WFH position with all necessary equipment provided. What You'll Do * Lead data management for complex, global clinical trials from study setup to database lock. * Serve as the main ...
From Home Clinical Data Coding information
See salary details
$19.95 - $25.59
4% of jobs
$25.59 - $31.23
10% of jobs
$31.23 - $36.87
2% of jobs
$36.87 - $42.50
4% of jobs
$45.32 is the 25th percentile. Wages below this are outliers.
$42.50 - $48.14
9% of jobs
$48.14 - $53.78
10% of jobs
The median wage is $58.48 / hr.
$53.78 - $59.42
13% of jobs
$59.42 - $65.06
17% of jobs
$66.72 is the 75th percentile. Wages above this are outliers.
$65.06 - $70.69
18% of jobs
$70.69 - $76.33
7% of jobs
$76.33 - $81.97
5% of jobs
$19
$57
$81
How much do from home clinical data coding jobs pay per hour?
What is a From Home Clinical Data Coding job?
What is the difference between From Home Clinical Data Coding vs From Home Medical Billing and Coding?
| Aspect | From Home Clinical Data Coding | From Home Medical Billing and Coding |
|---|---|---|
| Certifications | Certified Coding Specialist (CCS), Certified Professional Coder (CPC) | Certified Professional Biller (CPB), Certified Professional Coder (CPC) |
| Work Environment | Healthcare facilities, insurance companies, remote | Medical offices, insurance companies, remote |
| Industry Usage | Hospitals, clinics, healthcare providers | Medical practices, insurance companies, billing services |
From Home Clinical Data Coding focuses on translating medical records into standardized codes for patient care and billing, often requiring clinical knowledge. From Home Medical Billing and Coding involves processing insurance claims and billing procedures, emphasizing billing codes and insurance policies. Both roles are remote, require similar certifications, but serve different functions within healthcare administration.
What are some common challenges faced by professionals working in from-home clinical data coding roles, and how can they be addressed?
What are the key skills and qualifications needed to thrive as a From Home Clinical Data Coder, and why are they important?

Full-time
Medical, Life, Retirement, PTO
Posted 7 days ago
Job description
Position Summary:
The Senior Clinical Data Manager is responsible and manages all aspects of the clinical trial data management process from study start up to post database lock for assigned projects. Standard Operating Procedures / Work Instructions (SOPs/WIs); regulatory directives; study specific plans and guidelines will be followed. This position will also oversee and/or perform database development and testing.
Essential functions of the job include but are not limited to:
- Primary Data Management (DM) contact (Lead DM role) for assigned clinical project(s) / program(s), ensuring that there is back-up, continuity, responsiveness, and that tasks are performed in a timely manner. May support another Lead DM as a back-up and/or team member. May include DM oversight of sponsor programs.
- Oversee project data entry process including development of data entry guidelines, training, data entry quality and resourcing
- May perform quality control of data entry
- Provide input, assesses and manage timelines. Ensure that clinical data management deadlines are met with quality. Assess resource needs for assigned projects, as needed.
- Develop CRF specifications from the clinical study protocol and coordinate the review/feedback from all stakeholders
- May assist in building clinical databases
- Conduct database build UAT and maintain quality controlled database build documentation. Oversee overall quality of the clinical database.
- May specify requirements for all edit check types e.g. electronic, manual data review, edit checks, etc. Oversee development of the edit check specifications and manual data review specifications
- Responsible for creating, revising, appropriate versioning and maintaining data management documentation. Oversee completeness of data management documentation for the Trial Master File.
- Train clinical research personnel on the study specific CRF, EDC, and other project related items as needed.
- Review and query clinical trial data according to the Data Management Plan
- Perform line listing data review based on the guidance provided by the sponsor and/or Lead DM
- Run patient and study level status and metric reporting
- Perform medical coding of medical terms relative to each other in order to ensure medical logic and consistency
- Coordinate SAE/AE reconciliation
- Liaises with third-party vendors such as external data and EDC vendors in a projectmanager capacity in support of timelines and data-related deliverables
- May assist with SAS programming and quality control of SAS programs used in the Data Management department
- Identify and troubleshoot operational problems, issues, obstacles, and barriers for studies based on metrics data, audit reports, and input from project team members and other stakeholders
- May assist in reviewing and providing feedback on protocols, Statistical Analysis Plans (SAP) and Clinical Study Reports (CSRs), if required by the project
- Participate in the development and maintenance of Standard Operating Procedures (SOPs) and corresponding process documentation related to data management and database management activities
- May attend strategy meetings, bid defense prep meetings, bid defenses, capability presentations, potential client engagement meetings
- May review Request for Proposals (RFP), proposals, provide project estimates
- Provide leadership for cross-functional and organization-wide initiatives, where applicable
- Trains and ensures that all data management project team members have been sufficiently trained
- Communicate with study sponsors, vendors and project teams as needed regarding data, database or other relevant project issues
- May present software demonstrations/trainings, department/company training sessions, present at project meetings
- May require some travel
- Perform other duties as assigned
Qualifications:
Minimum Required:
- Bachelors and/or a combination of related experience
Other Required:
- 8+ years' experience as a Sr. Clinical Data Manager and 5 Years as a Clinical Data Manager II
- Proficiency in Microsoft Office: Word, Excel, PowerPoint, Outlook
- Able to handle a variety of clinical research tasks
- Excellent organizational and communication skills
- Professional use of the English language; both written and oral
- Experience in utilizing various clinical database management systems
- Broad knowledge of drug, device and/or biologic development and effective data management practices
- Strong representational skills, ability to communicate effectively orally and in writing
- Strong leadership and interpersonal skills
- Ability to undertake occasional travel
Preferred:
- Experience in a clinical, scientific or healthcare discipline
- Dictionary medical coding (MedDRA and WHODrug)
- Understanding of CDISC standards (CDASH, SDTM, ADaM, etc....)
- Oncology and/or Orphan Drug therapeutic experience
Precision is required by law in some states or cities to include a reasonable estimate of the compensation range for this role. This compensation range takes into account the wide range of factors that are considered in making compensation decisions including but not limited to: skill sets, experience and training, licensure and certifications, and other business and organizational needs. The disclosed range estimate has not been adjusted for the applicable geographic differential associated with the location at which the position may be filled. At Precision, it is not typical for an individual to be hired at or near the top of the range for their role and compensation decisions are dependent on the facts and circumstances of each case. This role is also eligible for a discretionary annual bonus, health insurance, retirement savings benefits, life insurance and disability benefits, parental leave, and paid time off for sick leave and vacation, among other benefits.
Reasonable estimate of the current range
$91,500-$166,100 USD
Any data provided as a part of this application will be stored in accordance with our Privacy Policy. For CA applicants, please also refer to our CA Privacy Notice.
Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law.
If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at QuestionForHR@precisionmedicinegrp.com.
It has come to our attention that some individuals or organizations are reaching out to job seekers and posing as potential employers presenting enticing employment offers. We want to emphasize that these offers are not associated with our company and may be fraudulent in nature. Please note that our organization will not extend a job offer without prior communication with our recruiting team, hiring managers and a formal interview process.
About Precision for Medicine
Sourced by ZipRecruiter
Industry
Biotechnology research and development
Company size
501 - 1,000 Employees
Headquarters location
Bethesda, MD, US
Year founded
2012