Artiva Biotherapeutics is seeking a Associate Director, Clinical Data Management to lead and scale our CDM function as we advance our NK cell therapy pipeline. This is a senior leadership role that ...
Artiva Biotherapeutics is seeking a Associate Director, Clinical Data Management to lead and scale our CDM function as we advance our NK cell therapy pipeline. This is a senior leadership role that ...
Job Duties Work collaboratively with other Data Managers, Programmers, Biostatisticians, Clinical Operations, Medical Directors, and Regulatory staff to meet project deliverables and timelines for ...
Job Duties Work collaboratively with other Data Managers, Programmers, Biostatisticians, Clinical Operations, Medical Directors, and Regulatory staff to meet project deliverables and timelines for ...
Job Duties Work collaboratively with other Data Managers, Programmers, Biostatisticians, Clinical Operations, Medical Directors, and Regulatory staff to meet project deliverables and timelines for ...
Job Duties Work collaboratively with other Data Managers, Programmers, Biostatisticians, Clinical Operations, Medical Directors, and Regulatory staff to meet project deliverables and timelines for ...
Director, Clinical Data & AI
Fort Worth, TX · On-site +1
The Director of Clinical Data & AI is the global functional leader responsible for the strategy ... Data management and data engineering * AI/ML and advanced analytics * Serve as the enterprise ...
Director, Clinical Data & AI
Fort Worth, TX · On-site +1
The Director of Clinical Data & AI is the global functional leader responsible for the strategy ... Data management and data engineering * AI/ML and advanced analytics * Serve as the enterprise ...
Senior Clinical Data Manager
Boston, MA · On-site
$130K - $196K/yr
Reporting to the Director of Clinical Data Sciences, you'll independently support active programs ... You'll serve as the primary data management voice on cross-functional study teams, partnering ...
Senior Clinical Data Manager
Boston, MA · On-site
$130K - $196K/yr
Reporting to the Director of Clinical Data Sciences, you'll independently support active programs ... You'll serve as the primary data management voice on cross-functional study teams, partnering ...
Clinical Data Manager
New York, NY · On-site
$115K - $145K/yr
About the Role We are looking for a Clinical Data Manager to accelerate Novellia's data curation and delivery processes. In this role, you will be responsible for working with a team of cross ...
Clinical Data Manager
New York, NY · On-site
$115K - $145K/yr
About the Role We are looking for a Clinical Data Manager to accelerate Novellia's data curation and delivery processes. In this role, you will be responsible for working with a team of cross ...
The Senior Clinical Data Manager will lead clinical data management activities for Repertoire ... into an Associate Director-level role as the organization continues to scale. The successful ...
Quick apply
The Senior Clinical Data Manager will lead clinical data management activities for Repertoire ... into an Associate Director-level role as the organization continues to scale. The successful ...
... manual data review of listings), SAE reconciliation, managing local laboratory and external labs and database lock. Perform Project Management : represent DM on clinical teams, coordinate ...
... manual data review of listings), SAE reconciliation, managing local laboratory and external labs and database lock. Perform Project Management : represent DM on clinical teams, coordinate ...
Senior Clinical Data Manager
Bridgewater, NJ · On-site +1
$90K - $130K/yr
Create and maintain clinical trial Data Management Study Binders. Perform Hands-on Data Management Activities * Design and review case report forms (CRFs/eCRFs). Develop and review Case Report Form ...
Senior Clinical Data Manager
Bridgewater, NJ · On-site +1
$90K - $130K/yr
Create and maintain clinical trial Data Management Study Binders. Perform Hands-on Data Management Activities * Design and review case report forms (CRFs/eCRFs). Develop and review Case Report Form ...
The Senior Clinical Data Manager is responsible for all aspects of the data management process from the development of project documentation, system set-up, User Acceptance Testing (UAT), routine ...
The Senior Clinical Data Manager is responsible for all aspects of the data management process from the development of project documentation, system set-up, User Acceptance Testing (UAT), routine ...
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Associate Clinical Data Manager
Maple Grove, MN · On-site
$40 - $50/hr
Associate Clinical Data Manager Location: Maple Grove, MN 55311 Work Arrangement: 100% Onsite Schedule: Monday-Friday, 8:00 AM-4:00 PM Contract Duration: 6 months, with a strong likelihood of ...
Posted today
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Be Seen First
Associate Clinical Data Manager
Maple Grove, MN · On-site
$40 - $50/hr
Associate Clinical Data Manager Location: Maple Grove, MN 55311 Work Arrangement: 100% Onsite Schedule: Monday-Friday, 8:00 AM-4:00 PM Contract Duration: 6 months, with a strong likelihood of ...
Posted today
Clinical Data Manager
Spring House, PA · On-site
Reports to Manager, Clinical Trial Management Business Support Internal interfaces: Study Teams ... IT Life Sciences Allied Healthcare CRO DIRECT # - 732-662-7964
Clinical Data Manager
Spring House, PA · On-site
Reports to Manager, Clinical Trial Management Business Support Internal interfaces: Study Teams ... IT Life Sciences Allied Healthcare CRO DIRECT # - 732-662-7964
Senior Clinical Data Manager
Malvern, PA · On-site
Position Summary The Senior Clinical Data Manager plays a pivotal role within Ocugen's clinical data management team. This individual will lead data management efforts, oversee quality data ...
Senior Clinical Data Manager
Malvern, PA · On-site
Position Summary The Senior Clinical Data Manager plays a pivotal role within Ocugen's clinical data management team. This individual will lead data management efforts, oversee quality data ...
The Senior Clinical Data Manager is responsible for all aspects of the data management process from the development of project documentation, system set-up, User Acceptance Testing (UAT), routine ...
The Senior Clinical Data Manager is responsible for all aspects of the data management process from the development of project documentation, system set-up, User Acceptance Testing (UAT), routine ...
Senior Clinical Data Manager
Malvern, PA · On-site
Position Summary The Senior Clinical Data Manager plays a pivotal role within Ocugen's clinical data management team. This individual will lead data management efforts, oversee quality data ...
Senior Clinical Data Manager
Malvern, PA · On-site
Position Summary The Senior Clinical Data Manager plays a pivotal role within Ocugen's clinical data management team. This individual will lead data management efforts, oversee quality data ...
Senior Clinical Data Manager
New Haven, CT · On-site
$133K - $173K/yr
Overview The Senior Clinical Data Manager is responsible for managing the data management activities for multiple clinical trials. Will work closely with internal team members and vendors to ensure ...
Senior Clinical Data Manager
New Haven, CT · On-site
$133K - $173K/yr
Overview The Senior Clinical Data Manager is responsible for managing the data management activities for multiple clinical trials. Will work closely with internal team members and vendors to ensure ...
Senior Clinical Data Manager
New Haven, CT · On-site
$133K - $173K/yr
The Senior Clinical Data Manager is responsible for managing the data management activities for multiple clinical trials. Will work closely with internal team members and vendors to ensure that ...
Senior Clinical Data Manager
New Haven, CT · On-site
$133K - $173K/yr
The Senior Clinical Data Manager is responsible for managing the data management activities for multiple clinical trials. Will work closely with internal team members and vendors to ensure that ...
Lead all data management (DM) activities for one or more clinical trials. * Contribute to ... Understands Company Policy and procedure to be able to guide direct reports appropriately, if ...
Lead all data management (DM) activities for one or more clinical trials. * Contribute to ... Understands Company Policy and procedure to be able to guide direct reports appropriately, if ...
Senior Clinical Data Manager
Dunkirk, NY · On-site
Position Summary The Senior Clinical Data Manager is an expert in clinical data management with demonstrated capability in building and maintaining clinical trial databases. They contribute to ...
Senior Clinical Data Manager
Dunkirk, NY · On-site
Position Summary The Senior Clinical Data Manager is an expert in clinical data management with demonstrated capability in building and maintaining clinical trial databases. They contribute to ...
Clinical Data Manager (P3)
Indianapolis, IN · On-site
$154K - $177K/yr
Eli Lilly and Company seeks a Clinical Data Manager (P3) to be accountable for the end-to-end clinical data sciences delivery for clinical studies, including clinical database build, data acquisition ...
Clinical Data Manager (P3)
Indianapolis, IN · On-site
$154K - $177K/yr
Eli Lilly and Company seeks a Clinical Data Manager (P3) to be accountable for the end-to-end clinical data sciences delivery for clinical studies, including clinical database build, data acquisition ...
Director Clinical Data Manager 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 director clinical data manager jobs pay per hour?

Full-time
Medical, Dental, Vision, Life, Retirement, PTO
Posted 14 days ago
Job description
We are a clinical-stage biotechnology company focused on developing natural killer (NK) cell-based therapies. Our mission is to develop effective, safe, and accessible cell therapies for patients with devastating autoimmune diseases. We aim to develop therapies that patients and physicians can utilize in a community setting. Our lead product candidate, AlloNK®, is a non-genetically modified, cryopreserved NK cell therapy being evaluated in combination with B-cell targeted monoclonal antibodies (mAbs). We believe the compelling cell killing properties of NK cells, when combined with mAbs for targeting, creates an opportunity to generate potentially transformative therapies.
For more information, visit www.artivabio.com.
Job Summary:
Artiva Biotherapeutics is seeking a Associate Director, Clinical Data Management to lead and scale our CDM function as we advance our NK cell therapy pipeline. This is a senior leadership role that combines hands-on program oversight with organizational accountability and serve as the internal subject matter expert on all things data management. This role is responsible for managing end-to-end data management activities across one or more clinical studies
Reporting to the Director or Head of Clinical Development Operations, the AD will be a key partner to Clinical Operations, Biostatistics, Translational Sciences, and Regulatory Affairs - driving quality, timelines, and innovation across Artiva's clinical data infrastructure. This is an ideal opportunity for a seasoned CDM leader who is energized by the opportunity to shape a function from the ground up in a high-impact, mission-driven organization.
Duties/Responsibilities:
Leadership & strategy
- Execute Artiva's CDM strategy - including technology platforms, data standards, vendor governance, and quality frameworks - in alignment with overall Clinical Development objectives
- Serve as the CDM functional representative on program teams and governance forums; partner with Clinical Operations, Biostatistics, Regulatory, and Translational Sciences to ensure integrated, inspection-ready data delivery
- Drive departmental SOPs, working practices, and process improvement initiatives; ensure the CDM function is prepared for internal audits and regulatory inspections
Program execution
- Provide senior oversight of all CDM activities across assigned programs from study start-up through database lock, ensuring timely delivery of high-quality, clean, and complete data
- Lead or oversee development and review of DM documents including CRFs, Data Management Plans, edit check specifications, Data Review Plans, and SAE reconciliation plans
- Lead Artiva UAT strategy and execution for EDC builds; ensure UAT standards are maintained across the program
- Manage and govern CRO and third-party vendor relationships for DM activities; oversee scope, quality, timelines, and budget; escalate and resolve issues proactively
- Drive program-level DM timelines; maintain cross-study visibility of milestones, risks, and resource needs; report status to leadership
- Coordinate and lead Artiva data quality reviews
- Participate in regular study and project team meetings
- Foster a culture of quality and continuous improvement
Standards & innovation
- Champion CDISC standards adoption (CDASH, SDTM) and EDC best practices across the organization
- Evaluate and implement tools and technologies that advance data quality, efficiency, and real-time data visibility (e.g., risk-based monitoring integration, data review automation)
- Mentor and develop CDM staff at all levels.
Requirements:
- 10+ years of clinical data management experience in pharma, biotech, or CRO, with 5+ years in progressive leadership roles
- Demonstrated experience managing and overseeing Data Management activities directly and through CRO/third-party service providers
- Deep expertise in EDC systems (Medidata Rave preferred) and clinical data standards (CDISC CDASH/SDTM, ICH GCP E6(R3), 21 CFR Part 11)
- Proven track record managing CRO and third-party DM vendor relationships across multiple concurrent studies
- Strong cross-functional communication and stakeholder management skills; ability to influence without authority at all levels of an organization
- Strong cross-functional communication and stakeholder management skills; ability to influence without authority at all levels of an organization
- Experience supporting regulatory submissions (IND, NDA/BLA) and/or inspection readiness activities preferred
- Bachelor's degree in life sciences, computer science, or related field; advanced degree a plus
In addition to a great culture, we offer:
- A beautiful facility
- An entrepreneurial, highly collaborative, and innovative environment
- Comprehensive benefits, including:
- Medical, Dental, and Vision
- Group Life Insurance
- Long Term Disability (LTD)
- 401(k) Retirement Plan
- Employee Assistance Program (EAP)
- Flexible Spending Account (FSA)
- Paid Time Off (PTO)
- Company paid holidays, including the year-end holiday week
- Our recognition program, Bonus.ly, is where you can trade in points earned for things you want.
If all this speaks to you, come join us on our journey!
Base Salary: $ 190,000 - $205,000. Exact compensation may vary based on level, skills and experience.
About Artiva Biotherapeutics
Sourced by ZipRecruiter
Industry
Biotechnology research and development
Company size
11 - 50 Employees
Headquarters location
San Diego, CA, US
Year founded
2019