Clinical Data Management Lead (Contract)

Kriyatx; North Carolina; Remote; USD 120,000 - 170,000; Part time

Job summary

Kriya Therapeutics, Inc. is seeking a Clinical Data Management Lead (Contract) to oversee operational data management across clinical programs. The role emphasizes hands-on data handling, data quality, and regulatory compliance with CROs and vendors in a fast-paced biotech setting.

The ideal candidate will have 8+ years of data management experience in pharma/biotech, expertise with CDISC standards, and strong collaboration skills to support regulatory submissions and study execution.

Qualifications

• Bachelor’s degree in life sciences or related field.
• 8+ years of clinical data management experience in pharma/biotech.
• Advanced degree preferred, or equivalent experience.
• Strong experience with Phase I–III trials; regulatory filings desirable.
• Solid knowledge of GCP, 21 CFR Part 11, and global regulatory requirements.
• Experience overseeing CROs and cross-functional teams.

Responsibilities

• Manage day-to-day clinical data management activities for assigned studies.
• Develop and maintain study data management plans and CRF guidelines; data validation specs.
• Lead CRO data management activities; ensure quality, timelines, and contracts.
• Serve as data management contact for cross-functional study teams; foster collaboration.
• Ensure FDA/ICH-GCP regulatory compliance across data activities.
• Design CRFs, databases, edit checks; collaborate with CRO partners.
• Oversee data reconciliation and data transfers (SAE, central lab, vendors).
• Support regulatory submissions with CDISC (CDASH/SDTM) compliance.
• Contribute to SOPs and best practices for data management.
• Assist audit readiness and TMF documentation.
• Identify process improvements to enhance efficiency and quality.
• Independently manage studies and escalate risks as needed.
• Provide data management input to study protocols and SAPs.

Skills

Bachelor’s degree in life sciences

8+ years of data management experience

GCP & 21 CFR Part 11 knowledge

Regulatory filings experience (IND/CTA

Cross-functional collaboration

CRO management experience

Data management for Phase I-III trials

Education

Bachelor’s degree in life sciences/related field

Advanced degree preferred

Tools

CDISC (CDASH/SDTM)

MedDRA/WHODrug dictionaries

Job description

Clinical Data Management Lead (Contract)

Department: Clinical

Employment Type: Contract

Location: Remote

Description

Kriya is a biopharmaceutical company whose mission is to develop life-changing gene therapies for diseases affecting millions of patients around the world.

We leverage our proprietary computational engine, in-house manufacturing infrastructure, and integrated design platform to engineer technologies and therapeutics with the potential to transform the treatment of a broad universe of diseases of high unmet need, with a focus on metabolic disorders, neurology, and ophthalmology.

We are proud to have been named Triangle Business Journal’s Life Sciences 2024 “Best Private Company to Work For,” recognized by Forbes as one of “America’s Best Startup Employers of 2024,” and honored as one of BioSpace’s “2025 Best Places to Work.”

Role Overview

The Clinical Data Management Lead (Contract) will be responsible for the operational execution of clinical data management activities across Kriya Therapeutics' clinical development programs. This role combines hands-on data management expertise with cross-functional coordination, ensuring data quality, integrity, and regulatory compliance throughout the product development lifecycle. The ideal candidate is a proactive and collaborative data management professional who thrives in a fast-paced biotech environment, demonstrates strong operational ownership, and effectively partners across internal teams, CROs, and external vendors to drive high-quality study execution.

Key Responsibilities

• Execute day-to-day clinical data management activities for assigned clinical studies, including database design, edit check development, data review, and database lock.
• Contributes to the development and maintenance of study-specific data management plans, CRF completion guidelines, data validation specifications, and data transfer agreements.
• Leads and proactively manages CRO data management activities, ensuring deliverables meet quality standards, timelines, and contractual obligations while identifying risks and driving resolution.
• Serves as the data management contact for cross-functional study teams, fostering strong collaboration and proactive communication between clinical operations, biostatistics, medical monitoring, regulatory affairs, CROs, and external vendors
• Ensure compliance with FDA, ICH-GCP, and other applicable regulatory requirements across all data management activities.
• Develop CRF designs, database structures, edit checks, and coding dictionaries (MedDRA, WHODrug) in collaboration with CRO partners.
• Conduct data reconciliation activities including SAE reconciliation, central lab data integration, and third-party vendor data transfers.
• Support preparation for regulatory submissions by ensuring data packages meet quality standards and timelines, including CDISC (CDASH, SDTM) compliance.
• Contribute to the development and maintenance of SOPs, work instructions, and best practices for clinical data management.
• Support audit and inspection readiness activities related to clinical data management, including TMF documentation.
• Identifies process improvement opportunities and contributes practical, solutions-oriented recommendations that enhance data management efficiency, quality, and study execution
• Independently manages assigned study activities while proactively escalating risks, maintaining organizational awareness, and supporting timely decision-making and issue resolution.
• Provide data management input into study protocols, statistical analysis plans, and clinical study reports.

Experience & Skills and Work Environment

Experience & Skills

• Bachelor's degree in life sciences, health informatics, computer science, or a related field.
• Minimum 8 years of clinical data management experience in the pharmaceutical/biotech industry.
• Advanced degree preferred, or equivalent professional experience.
• Strong expertise managing data for Phase I-III clinical trials; experience across multiple therapeutic areas a plus.
• Solid knowledge of GCP, 21 CFR Part 11, and global regulatory requirements.
• Experience supporting regulatory filings (e.g., IND, CTA, NDA, BLA) and global clinical trials desired.
• Experience working with or overseeing CROs performing data management activities is required.
• Demonstrated ability to work effectively in a collaborative and evolving biotech environment with strong organizational, communication, and relationship-management skills.
• Working knowledge of drug development processes from pre-IND through regulatory filing.
• Strong understanding of clinical trial protocols and data flow processes.
• Demonstrated problem-solving ability with strong organizational skills and attention to detail. Excellent written and verbal communication skills with the ability to build collaborative working relationships across functions and external partners are required.
• Self-motivated, adaptable, and willing to contribute in a hands-on manner within a growing and fast-paced organization.

Work Environment

• Primarily desk-based, generally in an office or home office setting.
• May involve extended periods of sitting and computer use.
• Ability to stand for extended hours.

Life at Kriya

Discover True Collaborative Teamwork
We have an ambitious set of goals, but our confidence – and our inspiration – stems from our people. From California to North Carolina, our teammates bring a spirit of Collaboration, Leadership, and Innovation to their work every day.

We’re always looking for teammates with the drive and energy to help us grow. If you want to be a part of a company with an entrepreneurial culture, a bold vision, and a meaningful purpose, join us.