Associate Director, Clinical Data Management
Company: Modex Therapeutics Ltd.
Location: Weston
Posted on: March 19, 2026
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Job Description:
Company Overview ModeX Therapeutics, an OPKO Health company, is
the leading clinical-stage biopharmaceutical company developing
unique and proprietary-multispecific therapeutics. Its MSTAR
platform unites the power of multiple biologics in a single
molecule to create multispecific antibodies that bind four or more
targets with unprecedented versatility and potency for complex
diseases. Its promising first-in-class immunology pipeline includes
candidates against immune diseases, including cancer (both solid
and hematologic tumors), immune impairment, as well as several of
the world's most pressing viral threats. Its founding team includes
globally recognized medical innovators with proven track records of
delivering breakthroughs for patients. ModeX is based in Weston,
Massachusetts. For more information, please visit www.modextx.com .
Job Description Job Summary: The Associate Director of Clinical
Data Management is a critical position within the ModeX clinical
operations team. This position is responsible for successfully
leading the execution of all data management activities, ensuring
focus on data integrity, validity, reliability in accordance with
standard processes, guidelines, industry best practices and
regulatory standards. This position may be involved in process
improvement initiatives to support the department and company in
achieving objectives and strategic goals. Key responsibilities
include but are not limited to: Lead all data management activities
from study start-up through final database lock for multiple
programs Create and track timelines for Data Management activities
Create and maintain the Data Management Plan Develop and design
Case Report Forms (CRFs) Develop Database Build specifications Lead
and execute Database Build and testing activities Define, build,
and test edit checks Perform data review and query
generation/resolution Process/reconcile electronic data received
from other data sources, Safety database, labs, etc. Database lock
and transfer process Track project progress and issue status
reports to ensure the achievement of key Data Management
milestones, such as database Go-Live and completion of tasks
towards Database Lock. Coordinate the work of CRO staff assigned to
the project. Ensure approved study documentation is maintained and
properly stored in the trial master files Develop or assist with
the project training development and delivery, for investigators,
clinical sites, project teams and CRO on data collection processes,
tools and/or equipment as required Act as point of escalation for
data related issues and queries Contribute to the continuous
improvement of DM and the wider organization through information
sharing, training and education May lead or participate in the
development, review and implementation of processes, policies, SOPs
and associated documents affecting DM May participate in and/or
lead DM and cross functional working groups Qualifications: BA/BS
degree required 7-10 years of experience in clinical research, drug
development, or other healthcare environment, including 5 years of
experience in data management Proven track record of oncology data
management excellence with a focus on quality and matrix team
environments Excellent teamwork, communication (verbal and
written), organizational, and interpersonal skills Self-motivated,
proactive, and able to prioritize and manage multiple initiatives
simultaneously Leadership / mentoring experience is a plus ModeX
Therapeutics is an Equal Opportunity Employer
Keywords: Modex Therapeutics Ltd., Chicopee , Associate Director, Clinical Data Management, Science, Research & Development , Weston, Massachusetts
