Clinical Trial Manager
3 weeks ago
Position Overview:
We are seeking a highly motivated individual to join our team as a Clinical Trial Manager (CTM) to maintain and co-ordinate the logistical aspects of clinical trials in compliance with Good Clinic Practice (GCP) and relevant Standard Operating Procedures (SOPs). The individual is an integral member of the study team who will facilitate operational efficiencies in clinical trials, guided by SOPs and ICH-GCP.
Prior to joining, your experience will have been from a clinical research organization, hospital or large medical specialty clinic, or work at another biopharma. You will be familiar with clinical data and clinical trial terminology, be able to read standard medical abbreviations that are used in the world of medical practice and clinical studies. You will have familiarity with FDA regulations, GCP, essential study documents, and key study activities such as tracking patient screening and enrollment, clinical laboratory sample collection, regulatory documents, and study team communications. Problem solving skills will be used daily. And did we mention - being highly organized is essential.
Reporting Relationship: This position will report to the Clinical Project Manager/Sr Clinical Project manager
About Inozyme Pharma:
Inozyme Pharma is a pioneering clinical-stage biopharmaceutical company dedicated to developing innovative therapeutics for rare diseases that affect bone health and blood vessel function. We are experts in the PPi-Adenosine Pathway, where the ENPP1 enzyme generates inorganic pyrophosphate (PPi), which regulates mineralization, and adenosine, which controls intimal proliferation (the overgrowth of smooth muscle cells inside blood vessels). Disruptions in this pathway impact the levels of these molecules, leading to severe musculoskeletal, cardiovascular, and neurological conditions, including ENPP1 Deficiency, ABCC6 Deficiency, calciphylaxis, and ossification of the posterior longitudinal ligament (OPLL).
Our lead candidate, INZ-701, is an ENPP1 Fc fusion protein enzyme replacement therapy (ERT) designed to increase PPi and adenosine, enabling the potential treatment of multiple diseases caused by deficiencies in these molecules. It is currently in clinical development for the treatment of ENPP1 Deficiency, ABCC6 Deficiency, and calciphylaxis. By targeting the PPi-Adenosine Pathway, INZ-701 aims to correct pathological mineralization and intimal proliferation, addressing the significant morbidity and mortality in these devastating diseases.
Essential Duties and Responsibilities:
Managing the supervision of contracted clinical research organizations, clinical laboratory vendors, and other outsourced work Leading both an internal and external/CRO study management team to ensure the successful conduct of clinical trials in accordance with State and Federal regulations, GCP regulations, ICH guidelines, and internal SOPs Authoring and reviewing as needed clinical study documents (Informed Consent Forms, Clinical Study Plans, Case Report Forms, etc.). Reviewing and contributing as needed to Investigator’s Brochure and other supportive regulatory documents Driving IRB/ethics committee and regulatory submissions as needed to support study timelines Effectively evaluating qualified study sites, performing site initiation, planning and presenting at investigator meetings/advisory boards, and implementing study start up activities, including development of documents related to conduct of the study (e.g., investigator binder, pharmacy binder, regulatory binder development, etc.) in collaboration with the clinical study team Managing and reviewing study budgets and investigator grants Overseeing interim study conduct, including management of operations/medical questions from CRO and sites, planning and facilitation of interim safety meetings, tracking subject recruitment, laboratory samples, and review of monitoring reports, and ensuring proper documentation is filed to meet GCP requirements Assessing study drug requirements and shipment logistics; contribute to labeling strategy Responsible for study close-out (CRO, third party vendors and internal close-out activities, invoice reconciliation for project closure) and ensuring study timelines are met Reviewing, and contributing as needed, to support completion of the Clinical Study Reports Overseeing TMF archival, submission and QC activities Working efficiently, both independently and within a team Training/mentoring junior staff by actively participating in documentation, sharing industry standards, implementation of trial conduct best practices, and lessons learned Creation, training, review and approval of clinical operations program specific documents May assist with the development of any new or updated SOPs/Work practices for the department Trains and mentor junior staff or peer mentorship of new hires Manages junior staffEducational Qualifications: Bachelor’s Degree required, relevant scientific or health-care related discipline highly preferred
Additional Qualifications:
Minimum of 4-6 years of clinical trial management experience, including protocol development, selection and management of CROs and contract vendors, timeline management, and budget management. Prior experience working in the biopharmaceutical industry is desired Thorough understanding and ability to lead a cross-functional team through all activities in the full clinical study life cycle Demonstrated proficiency in management of multi-center international clinical trials (from initiation to closure) Experience managing outsourced work Excellent interpersonal, communication (written and verbal), time management, presentation and organizational skills Management or mentorship experience desired Ability and willingness to travel 5-10% of the time (international and domestic) Notice: JavaScript is required for this content.-
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