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Associate Clinical Data Manager Jobs (NOW HIRING)

Pharmaron

Senior Clinical Data Manager

Somerset, NJ · On-site

$90K - $100K/yr

Position: Senior Clinical Data Manager FLSA Status: Exempt Location: Onsite (Somerset, New Jersey) Salary: $90,000 to $100,000 About Pharmaron Pharmaron is a global CRO (Contract Research ...

Trifecta Proven, LLC

$80K - $152K/yr

Trifecta Proven is recruiting for Clinical Data Managers (CDMs) to provider services at the National Institute of Health. There are multiple openings available. We are looking for Level I, II and II ...

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Cooper Companies

Lead Clinical Data Manager

San Ramon, CA · Hybrid

$164K - $219K/yr

Leads all aspects of clinical data management activities from study initiation through database lock and study closeout. Develops, optimizes and controls data management system, including external ...

Cytel

Principal Clinical Data Manager

Cambridge, MA · Remote

Principal Clinical Data Manager United States (Remote) Responsibilities - Responsible for vendor oversight activities across global development programs. - Represents data management function on the ...

Horizontal Talent

Clinical Data Manager II

Aliso Viejo, CA · Remote

$22 - $29.23/hr

Join our dynamic team as a Clinical Data Manager II, where you'll play a pivotal role in managing data for clinical studies from start to finish. This position offers an exciting opportunity to ...

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How much do associate clinical data manager jobs pay per hour?

As of Jul 12, 2026, the average hourly pay for associate clinical data manager in the United States is $38.95, according to ZipRecruiter salary data. Most workers in this role earn between $29.33 and $38.94 per hour, depending on experience, location, and employer.

What does an Associate Clinical Data Manager do?

An Associate Clinical Data Manager is responsible for collecting, cleaning, and managing clinical trial data to ensure its accuracy, integrity, and compliance with regulatory standards. They work closely with clinical teams to design data collection tools, monitor data quality, and resolve discrepancies. Their work is crucial in supporting the analysis and reporting of clinical trial results, which can impact decisions about new medical treatments.

What are the key skills and qualifications needed to thrive as an Associate Clinical Data Manager, and why are they important?

To thrive as an Associate Clinical Data Manager, you need a solid background in life sciences or related fields, strong analytical abilities, and attention to detail, often supported by a relevant bachelor's degree. Familiarity with clinical data management systems (CDMS), electronic data capture (EDC) tools like Medidata Rave, and an understanding of regulatory guidelines such as ICH-GCP are typically required. Excellent organizational skills, effective communication, and problem-solving abilities help you excel in managing complex datasets and collaborating across teams. These skills ensure data integrity, regulatory compliance, and smooth conduct of clinical trials, which are critical to successful drug development.

What are some common challenges an Associate Clinical Data Manager might face when working on multi-site clinical trials?

Associate Clinical Data Managers often encounter challenges such as ensuring data consistency across different trial sites and managing discrepancies that arise from varying data entry practices. Coordinating with site staff, monitoring data quality, and adhering to strict timelines require strong communication and organizational skills. Additionally, adapting to evolving regulatory requirements and new data management technologies can be demanding, but these challenges also offer valuable learning opportunities for career growth.
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Associate Clinical Data Manager jobs near you

Senior Clinical Data Manager, Clinical Data Science

Ionis

Carlsbad, CA • On-site

Full-time

Re-posted 22 days ago

Job description

Headquartered in Carlsbad, California, and with offices in Boston, Massachusetts, and Dublin, Ireland, Ionis has been at work for more than three decades discovering medical breakthroughs that have redefined life for people with serious diseases. We're pioneers in RNA-targeted medicines, and our platform continues to revolutionize drug discovery and transform lives for patients with unmet needs. With multiple marketed medicines and a leading pipeline in neurology, cardiology and select areas of high patient needs, we continue to drive innovation in RNA therapies in addition to advancing new approaches in gene editing to provide greater value to patients and are well positioned financially to deliver on our strategic goals.
At Ionis, we pride ourselves on cultivating a challenging, motivating and rewarding environment that fosters innovation and scientific excellence. We know that our success is a direct result of the exceptional talents and dedication of our employees.
With an unprecedented opportunity to change the course of human health, we look to add diverse individuals, skill sets and perspectives to our exceptional team. We continue to invest time, money and energy into making our onsite, hybrid and remote work environments a place where solid and lasting relationships are built and where our culture and employees can thrive.
We're building on our rich history, and we believe our greatest achievements are ahead of us. If you're passionate about the opportunity to have meaningful impact on patients in need, we invite you to apply and join us. Experience and contribute to our unique culture while you develop and expand your career!
SENIOR CLINICAL DATA MANAGER
CLINICAL DATA SCIENCE
SUMMARY:
The Senior Clinical Data Manager is responsible for all aspects of clinical data management throughout study conduct. The Senior Clinical Data Manager executes on policies and procedures for gathering, analyzing, and reporting clinical data for clinical trials that are conducted in compliance with Good Clinical Practice (GCP) and regulatory requirements.
RESPONSIBILITIES:
  • Acts as lead data manager within study team
  • Performs/oversees database development and management (e.g., CRF Specifications, Edit Check Specifications, Programming Specifications and QC, User Acceptance Testing, open, clean and lock of databases)
  • Support the adoption and implementation of Clinical Data Warehouse technology to enable streamlined CDM data review strategies
  • Implement Risk Management Planning on clinical studies
  • Authors, reviews and/or approves various study related documents and plans (e.g., Data Management Plans, Data Transfer Agreements, CRF Completion Guidelines, Manual Review Guidelines)
  • Manages and performs ongoing data management activities including CRF review, query generation, receipt and reconciliation of external data, SAE reconciliation, data listing generation and production of CDM summary reports (e.g. metrics) within projected study timelines.
  • 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 Practices (GCP)
  • Evaluates issues, recommend and implement solutions mitigation strategies as required
  • Assists or leads with vendor selection process for outsourced CDM activities
  • Oversees, as necessary, multiple External Service Provider (ESPs), contractors, or direct reports engaged to perform data management and EDC activities
  • Participates in governance of External Service Provider (ESPs) across studies
  • Participates in training of new hires and/or junior team members
  • Supports regulatory inspection activities
  • Oversees external data providers (e.g., IRT, central and specialty labs, patient diaries)
  • Presents at investigator's meetings and other data management trainings for study
  • Escalates study related issues and communicates as appropriate with management and other functions
  • Represents Clinical Data Management at study team meetings and facilitates cross-functional activities (e.g. Clinical Data Listing Reviews, database lock activities)
  • Proactively addresses operational issues and clinical data questions
  • Provides updates on study timelines, vendor oversight and other study related activities
  • Liaises with the document specialists to ensure data management files are filed appropriately
  • Implements best practices and industry standards across all data management activities
  • Assists and leads department initiatives, process improvements, and cross functional initiatives
  • Performs other duties, as appropriate
  • Travel is variable and estimated at 10-20% domestic and international

COMPETENCIES:
  • Excellent analytical and problem-solving skills
  • Excellent organizational and time-management skills with ability to multitask and prioritize
  • Strong interpersonal and communication skills
  • Ability to effectively develop and manage relationships with internal and external stakeholders
  • Excellent attention to detail
  • Flexible to changing priorities
  • Strong and positive work ethic

REQUIREMENTS:
  • Bachelor's Degree (BA/BS) preferred
  • Minimum of five (5) years of direct Clinical Data Management experience, including at least 2 years of Study Lead Data Manager responsibilities.
  • Experience with Electronic Data Capture (EDC) systems
  • Working knowledge of CDISC CDASH and CDISC SDTM standards/guidelines
  • Experience/training in the following areas: Good Clinical Practices (i.e. GxP Regulations; ICH Guidelines; Good Quality Practices), 21 CFR Part 11 and Computer Security (Part 11, Electronic Records; Electronic Signatures-Scope and Application; 21 CFR 11 and Industry Guidance; Computerized Systems Used in Clinical Trials), HIPAA, Drug Development and Approval Process, Data Management Overview
  • Proficiency in MS Office including Word, Excel, and PowerPoint required
  • Medical coding experience preferred but not required

Please visit our website, http://www.ionis.com for more information about Ionis and to apply for this position; reference requisition # IONIS003961
Ionis offers an excellent benefits package! Follow this link for more details: Ionis Benefits
Full Benefits Link: https://www.ionis.com/careers/working-at-ionis/#:~:text=our%20employee%20spotlight-,Benefits,-Employees%20are%20rewarded
The pay scale for this position is $95,000 to $151,418
NO PHONE CALLS PLEASE. PRINCIPALS ONLY.
Ionis Pharmaceuticals, Inc. and all its subsidiaries are proud to be EEO employers.
Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws.
For further information, please review the Know Your Rights notice from the Department of Labor.

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