Director, Data Management

Accenttx; Lexington (MA); On-site; USD 100,000 - 140,000; Full time

Job summary

A biopharmaceutical company in Lexington seeks a Director of Clinical Data Management. This role is pivotal for overseeing all data management activities in clinical trials, ensuring data integrity, completeness, and compliance with regulations. Candidates should have a Bachelor's degree in health sciences or a related field and 5 years of experience in clinical data management. Strong expertise in regulatory requirements and data management tools is essential for success in this role.

Qualifications

• 5+ years of progressive clinical data management experience in pharmaceutical or biotechnology environments.
• Experience with GCP, CDISC requirements, ICH, and FDA regulations.
• Hands-on experience with web-based Electronic Data Capture systems.

Responsibilities

• Lead data management activities across clinical trials.
• Ensure integrity and compliance of clinical trial data.
• Oversee CROs and monitor performance metrics.

Skills

Clinical trial processes

Data management principles

Regulatory requirements

Strong communication skills

Analytical abilities

Education

Bachelor’s degree in health sciences or related field

Advanced degree in a related field

Tools

EDC systems

SQL

SAS

R

Python

Job description

Accent Therapeutics is a biopharmaceutical company based in Lexington, MA that is focused on developing first in class and best in class small molecule inhibitors to primarily treat cancer. Founded in 2017, named as one of Fortune’s Top Ten Workplaces in Healthcare and Biopharma in 2020, and one of Fierce Biotech’s Fierce15 in 2020, Accent is building a highly collaborative team of experienced high-caliber drug developers to develop life-changing therapies for patients.

Position Summary

The Director, Clinical Data Management (CDM) is responsible for oversight, execution, and quality of all data management activities across assigned clinical trials from study start-up through database lock. This role ensures the integrity, completeness, and regulatory compliance of clinical trial data while leading cross-functional collaboration, CRO oversight, and continuous process improvement.

The CDM provides both operational leadership and strong technical expertise across the full data lifecycle, maintaining the highest standards of data quality in accordance with regulations.

Responsibilities

• Serve as the data management lead on cross-functional study teams.
• Oversee the collection, validation, reconciliation, and processing of clinical trial data from first patient through database lock.
• Ensure synchronization of data management timelines with overall clinical study timelines.
• Provide oversight of CROs and external service providers; monitor performance, deliverables, and quality metrics.
• Participate in vendor selection and contract evaluation for outsourced data management activities.
• Contribute to departmental initiatives, SOP development, process optimization, and technology enhancements.
• Develop, review, and approve key study documents, including the data management plan, case report forms, database build specifications, data transfer specifications, and SAE reconciliation plans.
• Design and oversee electronic Case Report Forms (eCRFs) and Electronic Data Capture (EDC) systems.
• Oversee database build, migration, updates, validation testing, and User Acceptance Testing (UAT).
• Develop and execute data validation checks and quality control procedures.
• Lead routine data review and cleaning, discrepancy management, and query generation/resolution.
• Generate and review data listings, summaries, metrics, and reports to support interim analyses and clinical study reports.
• Provide training on EDC systems, CRF completion guidelines, and data management processes to internal and external stakeholders.
• Contribute to a professional and collaborative working environment aligned with company values.

Required Qualifications

• Bachelor’s degree in health sciences, life sciences, mathematics, computer science, or a related scientific discipline; oncology/solid tumor clinical trial experience is a plus.
• ~5 years of progressive clinical data management experience in pharmaceutical, biotechnology, or CRO environments (depth of experience considered in lieu of minimum years).
• Strong expertise in clinical trial processes, data management principles, and regulatory requirements.
• Working knowledge of GCP, CDISC requirements, ICH, and FDA regulations.
• Hands-on experience with web-based Electronic Data Capture (EDC) systems and clinical data management platforms.
• Experience writing SQL queries to extract, review, and validate clinical trial data.
• Exposure to R and/or Python for data analysis, data review automation, or visualization.
• Experience with industry-standard dictionaries (MedDRA, WHO Drug).
• Familiarity with data analysis/reporting tools such as SAS, SQL, or similar systems.
• Excellent verbal and written communication skills.
• Strong analytical, problem-solving, and organizational abilities.

Preferred Qualifications

• Advanced degree in a related field.
• Experience contributing to or validating data management software tools.

Accent values diversity and is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person’s race, color, gender, age, religion, national origin, ancestry, disability, marital or veteran status, genetic information, sexual orientation or any other legally protected status. Accent will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.

Note to Third Party Staffing Agencies: Please do not forward any agency resumes. Accent Therapeutics is not responsible for any fees related to resumes that are unsolicited.