Green Card Senior Clinical Data Manager Jobs
Senior Clinical Data Manager roles qualify for employment-based green card sponsorship under EB-2 or EB-3, depending on your degree level and the employer's requirements. Sponsorship follows the PERM labor certification process, where your employer documents that no qualified U.S. worker is available before filing your I-140 immigrant petition.
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Get Access To All JobsPosition 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 project manager 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
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.
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 project manager 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
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.
See all Green Card Senior Clinical Data Manager Jobs
Sign up for free to unlock all listings, filter by visa type, and get alerts for new Green Card Senior Clinical Data Manager Jobs.
Get Access To All JobsTips for Finding Green Card Sponsorship as a Senior Clinical Data Manager
Document your CDM credentials before applying
Gather degree transcripts, CDISC certifications, and evidence of clinical trial systems experience before approaching employers. PERM requires precise credential matching between your qualifications and the posted job description, so gaps discovered later can restart the process.
Target sponsors with active PERM filing history
Pharmaceutical companies, CROs, and health systems that have filed PERM applications for data management roles understand the process. Search the DOL OFLC disclosure data by SOC code 15-2051 to identify employers with recent EB-2 or EB-3 filings for similar positions.
Search verified sponsoring employers on Migrate Mate
Use Migrate Mate to filter Senior Clinical Data Manager openings by green card sponsorship history. This cuts the time spent cold-applying to employers who have never navigated PERM for clinical data roles.
Verify your role meets EB-2 advanced-degree requirements
EB-2 classification requires the position to normally require a master's degree or equivalent. If your employer posts the role as requiring only a bachelor's plus five years of experience, confirm with their immigration counsel whether EB-2 or EB-3 is the appropriate category before accepting an offer.
Request PERM timeline commitments during offer negotiation
PERM labor certification typically takes six to twelve months before the I-140 is even filed. Ask your prospective employer when they plan to initiate the process and whether they'll cover premium processing for the I-140 to reduce uncertainty while you're waiting.
Check your priority date against the Visa Bulletin early
EB-3 green card backlogs vary significantly by country of birth. If you're from India or China, your priority date determines when you can file for adjustment of status, potentially adding years after PERM approval. Review the monthly Visa Bulletin from USCIS before committing to a sponsorship timeline.
Green Card Senior Clinical Data Manager: Frequently Asked Questions
Do Senior Clinical Data Manager roles typically qualify for EB-2 or EB-3 green card sponsorship?
Most Senior CDM positions qualify for EB-2 when the employer requires a master's degree or a bachelor's degree plus substantial progressive experience equivalent to an advanced degree. EB-3 applies when the role requires only a bachelor's degree. The sponsoring employer's job description and your credentials together determine the category, and USCIS makes the final classification decision when reviewing the I-140 petition.
How does green card sponsorship differ from H-1B sponsorship for this role?
H-1B visa is a temporary work visa with a three-year initial period, an annual lottery for cap-subject positions, and no path to permanence on its own. PERM-based green card sponsorship has no annual cap at the petition stage, is employer-initiated, and leads directly to lawful permanent residency. The tradeoff is time: PERM plus I-140 filing typically takes one to two years before adjustment of status can even begin, compared to H-1B approval in a few months.
What does the PERM process require from me as the candidate?
Your primary obligation is providing accurate credential documentation: official transcripts, certifications such as CDISC or SAS, and employment verification letters covering prior CDM experience. The employer and their immigration attorney handle the DOL PERM application and recruitment steps, but they'll need to match your qualifications precisely to the posted job requirements. Any discrepancy between your credentials and the PERM application can trigger an audit.
How can I find Senior Clinical Data Manager jobs that offer green card sponsorship?
Migrate Mate is built specifically to surface roles at employers with green card sponsorship history, so you can filter Senior CDM openings by EB-2 or EB-3 sponsorship rather than sifting through postings that don't mention immigration support. This is more targeted than general job searches because it screens for employers who have already demonstrated willingness to navigate PERM for clinical data roles.
Does my country of birth affect how long the green card process takes for this role?
Yes, significantly. The employment-based green card backlog is determined by country of birth, not citizenship. Candidates born in India or China face multi-year waits even after PERM and I-140 approval because demand from those countries exceeds the annual per-country visa limits. Candidates born in most other countries generally face much shorter waits or no backlog at all. USCIS publishes the monthly Visa Bulletin, which shows current priority dates by country and preference category.