Senior Clinical Data Manager

Repertoire Immune Medicines•Cambridge, MA

12d•Hybrid

About The Position

Repertoire Immune Medicines is a clinical-stage biotechnology company focused on developing transformative therapies for cancer and autoimmune disease by harnessing the power of the human immune system. The company utilizes its proprietary DECODE TM platform to map the immune synapse and translate biological insights into targeted immune medicines. Repertoire has established collaborations with major pharmaceutical companies and is advancing a pipeline of TCR bispecific immunotherapies. The Senior Clinical Data Manager will be instrumental in supporting these programs by leading clinical data management activities for Repertoire-sponsored clinical trials from initiation through to archival and submission support. This role involves hands-on data management expertise, oversight of CROs and vendors, and close collaboration with various internal departments and external partners to ensure timely, accurate, complete, and inspection-ready clinical trial data in compliance with GCP, ICH guidelines, and other relevant regulations. The ideal candidate will possess strong CDM expertise, excellent judgment for identifying and escalating data quality risks, and the ability to translate protocol requirements into effective data collection and review strategies. This position requires a high degree of ownership, a proactive approach, and a commitment to patient safety, data integrity, and regulatory-quality execution within a fast-paced biotech environment. A collaborative, in-person team culture is valued, with an expectation to work on-site in the Cambridge office at least three days per week.

Requirements

Bachelor’s degree in life sciences, health sciences, computer science, data science, or a related field.
Minimum of 7 years of clinical data management experience in industry-sponsored clinical trials, with significant hands-on study lead experience from study start-up through database lock.
Experience providing sponsor oversight of CROs and third-party vendors, including external data transfer specifications, reconciliation, and data cleaning metrics.
Hands-on experience with Medidata Rave, including eCRF design review, edit check review, UAT, query management, data exports, user access review, and database change control.
Strong understanding of clinical data management practices, GCP, ICH guidelines, FDA requirements, and related global regulatory expectations.
Working knowledge of CDISC standards (CDASH, SDTM, ADaM) and how database design supports downstream SDTM mapping and regulatory submission readiness.
Experience with MedDRA and WHODrug coding oversight.
Strong project management skills, with the ability to manage timelines, deliverables, risks, issues, and cross-functional communication.

Nice To Haves

Experience supporting oncology trials, including RECIST-based tumor assessments, prior therapies, PK/PD, immunogenicity, biomarkers, and central imaging data preferred.

Responsibilities

Develop and maintain key data management documents, including the Data Management Plan, eCRF specifications, completion guidelines, edit check specifications, data validation plan, data transfer specifications, external data reconciliation plans, medical coding plan, and database lock plan.
Establish and track data management timelines, deliverables, milestones, risks, and mitigation plans; provide regular updates to management.
Oversee and provide hands-on review of Medidata Rave eCRF design, database build, edit checks, testing, UAT, go-live, change control, and database lock activities, including approval of database change requests during study conduct.
Ensure eCRF design and database structure support protocol requirements, efficient data cleaning, SDTM mapping, and regulatory submission readiness; apply CDASH principles and maintain alignment with CDISC standards (SDTM, ADaM).
Oversee data cleaning and lead cross-functional data review — including adverse events, serious adverse events, concomitant medications, laboratory data, exposure, dose modifications, tumor assessments, and protocol deviations — to ensure data are accurate, complete, traceable, and available in support of safety surveillance, regulatory reporting, and clinical decision-making.
Serve as primary point of contact and provide sponsor oversight of CRO data management activities and third-party vendors (IRT, central and local laboratory, imaging, safety, PK/PD, biomarker, genomic, and specialty testing), ensuring deliverables meet Repertoire quality expectations and align with protocol requirements, data standards, regulatory expectations, and study timelines.
Monitor CRO and vendor performance metrics (query aging, data cleaning, external data transfers, reconciliation, coding, database lock readiness) and escalate data quality, timeline, or vendor performance issues as needed.
Oversee medical coding (MedDRA, WHODrug) and risk-based data quality review through listings, dashboards, metrics, trend analyses, and issue escalation.
Ensure data management activities comply with GCP, ICH guidelines, FDA and global regulatory requirements, GDPR, HIPAA, and Repertoire SOPs; champion data integrity, traceability, and inspection readiness across all data management deliverables.
Maintain Trial Master File documentation; support audits, inspections, and regulatory submissions; and lead or participate in process improvement initiatives that enhance data quality, efficiency, and scalability across clinical trials.