Position Summary The Clinical Data Manager is an expert in clinical data management with ... Coding Guidelines * Annotated CRFs * Edit Check Specifications * Attend study-specific team ...
Position Summary The Clinical Data Manager is an expert in clinical data management with ... Coding Guidelines * Annotated CRFs * Edit Check Specifications * Attend study-specific team ...
Clinical Data Manager
Burlington, MA · On-site
$145K - $160K/yr
Produce medical monitor, coding listings and ad hoc listings for team review (Jreview, SAS ... Minimum of 5 years of experience in clinical data management within the pharmaceutical or ...
Clinical Data Manager
Burlington, MA · On-site
$145K - $160K/yr
Produce medical monitor, coding listings and ad hoc listings for team review (Jreview, SAS ... Minimum of 5 years of experience in clinical data management within the pharmaceutical or ...
Clinical Data Analyst
$105K - $115K/yr
The Clinical Data Analyst partners with clinical leadership, payor relations, and operations to ... Compliance with Centria's Code of Conduct, policies and procedures, and Federal and State laws.
Clinical Data Analyst
$105K - $115K/yr
The Clinical Data Analyst partners with clinical leadership, payor relations, and operations to ... Compliance with Centria's Code of Conduct, policies and procedures, and Federal and State laws.
Clinical Data Analyst
Farmington Hills, MI · On-site
$105K - $115K/yr
The Clinical Data Analyst partners with clinical leadership, payor relations, and operations to ... Compliance with Centria's Code of Conduct, policies and procedures, and Federal and State laws.
Clinical Data Analyst
Farmington Hills, MI · On-site
$105K - $115K/yr
The Clinical Data Analyst partners with clinical leadership, payor relations, and operations to ... Compliance with Centria's Code of Conduct, policies and procedures, and Federal and State laws.
Clinical Data Analyst
$105K - $115K/yr
The Clinical Data Analyst partners with clinical leadership, payor relations, and operations to ... Compliance with Centria's Code of Conduct, policies and procedures, and Federal and State laws.
Quick apply
Clinical Data Analyst
$105K - $115K/yr
The Clinical Data Analyst partners with clinical leadership, payor relations, and operations to ... Compliance with Centria's Code of Conduct, policies and procedures, and Federal and State laws.
Clinical Data Manager
Chicago, IL · On-site +1
$50 - $60/hr
... clinical trial ... The role will oversee CRO partners, EDC build and validation, external data processing, coding ...
Clinical Data Manager
Chicago, IL · On-site +1
$50 - $60/hr
... clinical trial ... The role will oversee CRO partners, EDC build and validation, external data processing, coding ...
Clinical Data Manager
Chicago, IL · On-site +1
$50 - $60/hr
... clinical trial ... The role will oversee CRO partners, EDC build and validation, external data processing, coding ...
Clinical Data Manager
Chicago, IL · On-site +1
$50 - $60/hr
... clinical trial ... The role will oversee CRO partners, EDC build and validation, external data processing, coding ...
Clinical Data Manager
Aliso Viejo, CA · On-site
$45 - $48/hr
Clinical Data Manager Location: Aliso Viejo, CA - Onsite Type: W2 Contract Rate: $45-48/Hr The ... Generate reports or data listings for study teams as needed. * Assist medical coding, AE/SAE ...
New
Clinical Data Manager
Aliso Viejo, CA · On-site
$45 - $48/hr
Clinical Data Manager Location: Aliso Viejo, CA - Onsite Type: W2 Contract Rate: $45-48/Hr The ... Generate reports or data listings for study teams as needed. * Assist medical coding, AE/SAE ...
New
Performs medical coding of data using MedDRA & WHODrug dictionaries * Ensures clinical data management activities are executed in compliance with regulatory authority requirements and Good Clinical ...
Performs medical coding of data using MedDRA & WHODrug dictionaries * Ensures clinical data management activities are executed in compliance with regulatory authority requirements and Good Clinical ...
Performs medical coding of data using MedDRA & WHODrug dictionaries * Ensures clinical data management activities are executed in compliance with regulatory authority requirements and Good Clinical ...
Performs medical coding of data using MedDRA & WHODrug dictionaries * Ensures clinical data management activities are executed in compliance with regulatory authority requirements and Good Clinical ...
Clinical Data Manager
Covington, KY · On-site +1
Finally, they will coordinate the receipt and processing of information for projects (e.g., coding ... Clinical data review * Provide or arrange for adequate project-specific training for the CDM team ...
Clinical Data Manager
Covington, KY · On-site +1
Finally, they will coordinate the receipt and processing of information for projects (e.g., coding ... Clinical data review * Provide or arrange for adequate project-specific training for the CDM team ...
Performs medical coding of data using MedDRA & WHODrug dictionaries * Ensures clinical data management activities are executed in compliance with regulatory authority requirements and Good Clinical ...
Performs medical coding of data using MedDRA & WHODrug dictionaries * Ensures clinical data management activities are executed in compliance with regulatory authority requirements and Good Clinical ...
Manager, Clinical Data Management
South Boston, MA · On-site
$123K - $133K/yr
Perform and/or review medical coding and SAE reconciliation. * Support internal review/QC of clinical data. * Support GCP inspection readiness. Minimum Qualifications * Bachelor's degree in a health ...
Manager, Clinical Data Management
South Boston, MA · On-site
$123K - $133K/yr
Perform and/or review medical coding and SAE reconciliation. * Support internal review/QC of clinical data. * Support GCP inspection readiness. Minimum Qualifications * Bachelor's degree in a health ...
The Director, Clinical Data Management, will be required to collaborate closely with other ... coding processing, protocol deviation collection, query management to identify errors and ...
The Director, Clinical Data Management, will be required to collaborate closely with other ... coding processing, protocol deviation collection, query management to identify errors and ...
Manager, Clinical Data Management
$123K - $133K/yr
Perform and/or review medical coding and SAE reconciliation. * Support internal review/QC of clinical data. * Support GCP inspection readiness. Minimum Qualifications * Bachelor's degree in a health ...
Manager, Clinical Data Management
$123K - $133K/yr
Perform and/or review medical coding and SAE reconciliation. * Support internal review/QC of clinical data. * Support GCP inspection readiness. Minimum Qualifications * Bachelor's degree in a health ...
Manager, Clinical Data Management
Boston, MA · On-site
$123K - $133K/yr
Perform and/or review medical coding and SAE reconciliation. * Support internal review/QC of clinical data. * Support GCP inspection readiness. Minimum Qualifications * Bachelor's degree in a health ...
Manager, Clinical Data Management
Boston, MA · On-site
$123K - $133K/yr
Perform and/or review medical coding and SAE reconciliation. * Support internal review/QC of clinical data. * Support GCP inspection readiness. Minimum Qualifications * Bachelor's degree in a health ...
Lead Clinical Data Manager
Manhattan, NY · Remote
Experience with medical coding dictionaries ( MedDRA, WHO Drug ). Minimum of 3+ years of lead or project management experience in clinical data management. Skills Excellent attention to detail and ...
Lead Clinical Data Manager
Manhattan, NY · Remote
Experience with medical coding dictionaries ( MedDRA, WHO Drug ). Minimum of 3+ years of lead or project management experience in clinical data management. Skills Excellent attention to detail and ...
Coding and Classification: Apply knowledge of medical coding systems (e.g., ICD-10, MedDRA, CPT, HCPCS) and standard of care guidelines, to interpret, classify and categorize abstracted clinical data ...
Coding and Classification: Apply knowledge of medical coding systems (e.g., ICD-10, MedDRA, CPT, HCPCS) and standard of care guidelines, to interpret, classify and categorize abstracted clinical data ...
Coding and Classification: Apply knowledge of medical coding systems (e.g., ICD-10, MedDRA, CPT, HCPCS) and standard of care guidelines, to interpret, classify and categorize abstracted clinical data ...
Quick apply
Coding and Classification: Apply knowledge of medical coding systems (e.g., ICD-10, MedDRA, CPT, HCPCS) and standard of care guidelines, to interpret, classify and categorize abstracted clinical data ...
OR · On-site
Coding and Classification: Apply knowledge of medical coding systems (e.g., ICD-10, MedDRA, CPT, HCPCS) and standard of care guidelines, to interpret, classify and categorize abstracted clinical data ...
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 clinical data coding jobs pay per hour?
What is a Clinical Data Coding job?
What are the key skills and qualifications needed to thrive in the Clinical Data Coding position, and why are they important?
What does a typical day look like for someone working in Clinical Data Coding?

Full-time
Medical, Dental, Vision, Life, Retirement, PTO
Posted 27 days ago
Job description
ImmunityBio, Inc. (NASDAQ: IBRX) is a commercial-stage biotechnology company developing cell and immunotherapy products that are designed to help strengthen each patient's natural immune system, potentially enabling it to outsmart the disease and eliminate cancerous or infected cells. We envision a day when we no longer fear cancer, but can conquer it, thanks to the biological wonder that is the human immune system. Our scientists are working to develop novel therapies that harness that inherent power by amplifying both branches of the immune system, attacking cancerous or infected cells today while building immunological memory for tomorrow. The goal: to reprogram the patient's immune system and treat the host rather than just the disease.
Why ImmunityBio?
• ImmunityBio is developing cutting-edge technology with the goal to transform the lives of patients with cancer and develop next-generation therapies and vaccines that complement, harness and amplify the immune system to defeat cancers and infectious diseases.
• Opportunity to join a publicly traded biopharmaceutical company with headquarters in Southern California.
• Work with a collaborative team with the ability to work across different areas of the company.
• Ability to join a growing company with professional development opportunities.
Position Summary
The Clinical Data Manager is an expert in clinical data management with demonstrated capability in building and maintaining clinical trial databases. They contribute to process improvements and initiatives within the Biometrics department as well as mentor and train junior staff members as applicable.
Essential Functions
- Create and/or review study-specific electronic or paper Case Report Forms (CRFs) using prior knowledge, protocol-specific information, and departmental standards. Work efficiently to incorporate core clinical team input and produce CRFs in a timely manner.
- Configure, migrate, and test electronic data capture (EDC) databases based on internal procedures, study requirements, and system best practices. Serve as a database manager for the study-specific clinical team, including the compilation of edit checks.
- Develop database requirements for use by EDC vendors. Serve as a study database manager and work with vendors to obtain deliverables in a timely manner.
- Create and/or review study-specific data management and database documentation, which may include:
- Data Management Plan
- CRF Completion Guidelines
- Coding Guidelines
- Annotated CRFs
- Edit Check Specifications
- Attend study-specific team meetings and produce status reports and requested metrics, which may include query information or data trends.
- Perform data review and query generation/closure.
- Perform coding of verbatim terms such as adverse events and concomitant medications. Collaborate with medical scientists for coding, consistency, review, and approval. Incorporating coding files into the clinical database.
- Participate in the development of new processes or revision of existing processes.
- Train internal colleagues in clinical data management in either informal or formal settings as needed.
- Train Investigators and/or Study Coordinators at Investigator Meeting on the CRFs, the EDC system, and the CRF completion guidelines as needed.
- Provide data management expertise and support to the clinical teams using data management best practices.
- Provide analytical insight into data management strategies and advise the internal team with tactical strategies accordingly.
- As necessary, provide work direction, guidance, mentoring, influence, and support to junior staff. Train junior staff in more complex clinical data management processes.
- Adhere to Standard Operating Procedures (SOPs), process improvements, and standardization of templates.
- Perform ad-hoc and cross-functional projects assigned to support business needs and provide developmental opportunities.
Education & Experience
- Bachelor's Degree in a science-related field with 4+ years of experience; or
- High school diploma with 8+ year of relevant experience.
- 4+ years of clinical data management experience required.
- Experience working with EDC clinical databases required.
- Veeva Vault CDMS and TrialMaster experience preferred.
- MedDRA and WHO Drug coding experience preferred.
Knowledge, Skills, & Abilities
- Working knowledge of clinical research, Good Clinical Practices, and regulatory requirements
- Knowledge of CDISC/STDM standards.
- Excellent English verbal and written communication skills; good organizational and interpersonal skills.
Working Environment / Physical Environment
- This position works onsite or remote based on the candidate's location
- Regular work schedule is Monday - Friday, within standard business hours. Flexibility is available with manager approval.
- Must possess mobility to work in a standard office setting and to use standard office equipment, including a computer
- Lift and carry materials weighing up to 20 pounds
This position is eligible for a discretionary bonus and equity award. The annual base pay range for this position is below. The specific rate will depend on the successful candidate's qualifications, prior experience as well as geographic location.
National Market (all markets unless identified as Premium)
$103,500 (entry-level qualifications) to $115,000 (highly experienced) annually
Premium Market (Premium markets include Los Angeles, San Diego, San Francisco, New York City, Chicago, & Boston)
$108,500 (entry-level qualifications) to $120,000 (highly experienced) annually
The application window is anticipated to close on 60 days from when it is posted or sooner if the position is filled or closed.
ImmunityBio employees are as valuable as the people we serve. We have built a resource of robust benefit offerings to best support the total wellbeing of our team members and their families. Our competitive total rewards benefits package, for eligible employees, include: Medical, Dental and Vision Plan Options • Health and Financial Wellness Programs • Employer Assistance Program (EAP) • Company Paid and Voluntary Life/AD&D, Short-Term and Long-Term Disability • Healthcare and Dependent Care Flexible Spending Accounts • 401(k) Retirement Plan with Company Match • 529 Education Savings Program • Voluntary Legal Services, Identity Theft Protection, Pet Insurance and Employee Discounts, Rewards and Perks • Paid Time Off (PTO) includes: 11 Holidays • Exempt Employees are eligible for Unlimited PTO • Non-Exempt Employees are eligible for 10 Vacation Days, 56 Hours of Health Pay, 2 Personal Days and 1 Cultural Day • We are committed to providing you with the tools and resources you need to optimize your Health and Wellness.
At ImmunityBio, we are an equal opportunity employer dedicated to diversity in the workplace. Our policy is to provide equal employment opportunities to all qualified persons without regard to race, gender, color, disability, national origin, age, religion, union affiliation, sexual orientation, veteran status, citizenship, gender identity and/or expression, or other status protected by law.
About ImmunityBio
Sourced by ZipRecruiter
Industry
Biotechnology research and development
Company size
51 - 200 Employees
Headquarters location
San Diego, CA, US
Year founded
2014