What are the responsibilities and job description for the Clinical Trial Manager (CTM) position at ModeX Therapeutics, Inc.?
The Clinical Trial Manager (CTM) is a valued position within the ModeX clinical operations team. The primary role of this position is to ensure all trial deliverables are met according to timelines, budget, operational procedures, and quality standards (e.g., GCP, ICH and ModeX standards). This includes independent responsibilities associated with planning, start-up, maintenance, and closeout of clinical trials.
Key responsibilities include but are not limited to:
- Oversight of the successful implementation, management, and closeout of ModeX clinical studies
- Support the clinical protocol development process in collaboration with the Head of Clinical Operations and the Medical Monitor
- Contribute in the development of clinical protocols, amendments, and related documents; drive and/or contribute to the development of trial-related documents and processes
- Assist in the management of 3rd party vendors with primary focus on the CRO
- Lead the development of study tools, guidelines, and training materials to support effective and accurate execution of clinical trial activities
- Develop relationships with Investigators and Site Staff as primary contact for clinical conduct of the trial
- Under the guidance of the Head of Clinical Operations, manage study start-up activities including regulatory documents, budget, and clinical trial agreements.
- Participate in the ongoing review and cleaning of the clinical trial data.
- Chair study team meetings, collecting input from all functional lines.
- Participate in site identification; attending PSVs and SIVs
- Oversee tracking, logistics, and quality operations for biological samples supporting clinical trials from collection to analysis ensuring that sample inventories are accurate, complete, and up-to-date
through effective interactions with internal teams, sites, central reference labs, specialty lab partners, external collaborators (e.g. Academia) and third-party vendors
- Oversee management of accurate enrollment log/trial allocations forms
- Ensure compliance with patient consent for collection and intended use, destruction, storage and/or future, post-study use of biological samples
- Communicate with management to ensure transparency throughout the course of the trial(s) regarding study metrics and overall status
- Participate in process improvement projects (as necessary)
Qualifications:
- BA/BS degree required
- The successful candidate should have a minimum of 4 years of experience in clinical drug development or clinical trial execution with exposure to biomarkers or immunogenicity sample activities including sample collection procedures and logistics considerations
- Advanced skills in Microsoft Office programs as well as good working knowledge of electronic data systems
- Detailed and precise record keeping skills are essential as well as the ability to track and resolve issues
- Excellent teamwork, communication (verbal and written), organizational, and interpersonal skills
- Self-motivated, proactive, and able to prioritize and manage multiple projects simultaneously
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.
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