Senior Clinical Trial Associate

4D Molecular Therapeutics

About The Position

4DMT is a leading late-stage biotechnology company advancing durable and disease-targeted therapeutics with potential to transform treatment paradigms and provide unprecedented benefits to patients. The Company’s lead product candidate 4D-150 is designed to be a backbone therapy forming the foundation of treatment of blinding retinal vascular diseases by providing multi-year sustained delivery of anti-VEGF (aflibercept and anti-VEGF-C) with a single, safe, intravitreal injection, which substantially reduces the treatment burden associated with current bolus injections. The Company’s lead indication for 4D-150 is wet age-related macular degeneration, which is currently in Phase 3 development, and second indication is diabetic macular edema. The Company’s second product candidate is 4D-710, which is the first known genetic medicine to demonstrate successful delivery and expression of the CFTR transgene in the lungs of people with cystic fibrosis after aerosol delivery GENERAL SUMMARY 4DMT seeks a motivated and experienced Senior Clinical Trial Associate to support the Company's clinical trial activities. This position reports to the Director, Clinical Operations, Retina and will be responsible for supporting the day-to-day operations of a phase 3 clinical trial including trial start up, conduct and close-out activities. This role requires strong, professional written and verbal communication skills, good organization and attention to detail, and the ability to consistently provide high quality work while managing competing priorities and maintaining tight timelines. This person must be interested in working in a fast-paced, team-oriented environment and be willing to work beyond their job scope to achieve department and company objectives.

Requirements

A./B.S. degree required
At least 2 years of work experience supporting clinical trials
Must be proficient with TMF and Veeva Vault
Proficient computer skills, specifically with Microsoft Office Suite that include Word, Excel, PowerPoint, and Outlook
Ability to prioritize and manage competing priorities
Team oriented and ability to effectively collaborate with study team, cross-functional team members, and external partners
Basic knowledge of clinical trial operations, ICH GCP Guidelines and other applicable regulatory requirements
Willing to travel as business needs demand (<5% anticipated)
Repetitive motions: Making substantial movements (motions) of the wrists, hands, and/or fingers. Fingering: Picking, pinching, typing or otherwise working, primarily with fingers rather than with whole hand or arm as in handling. Talking: Expressing or exchanging ideas by means of the spoken word.
Sedentary work: Exerting up to 10 pounds of force occasionally and/or a negligible amount of force frequently or constantly to lift, carry, push, pull or otherwise move objects, including the human body. Sedentary work involves sitting most of the time. Jobs are sedentary if walking and standing are required only occasionally, and all other sedentary criteria are met.
The worker is not substantially exposed to adverse environmental conditions (as in typical office or administrative work).

Responsibilities

Collect, track and conduct initial review for completeness of site regulatory documents for IP release and/or TMF filing
Maintain multiple tracking spreadsheets following the progress of assigned clinical trials, such as study subject tracking, essential document tracking, and sample and investigational product tracking
Track and coordinate CRO and third-party vendor activities, including vendor provided meeting minutes, study updates and trackers
Assist with tracking of clinical trial progress including status update reports, as requested
Assist in tracking of trial IP
Assist in tracking of clinical lab samples and central reader/lab data, including tracking of sample shipments and reconciliation
May assist CTM in tracking and follow-up of monitoring visit reports and unresolved issues
Facilitate review and execution of new CDAs, contracts and Work Orders through established legal approval process (CTAs, MSAs, work/task orders)
Perform first pass review of all site and vendor invoices including tracking and generation of monthly/quarterly accruals for finance
Communicate directly with sites, Contract Research Organizations (CROs) and field CRA/monitors to obtain updated information, essential documents, etc. to assist with driving start-up, study conduct, and/or close-out activities
Assist with the organization, management and conduct of internal team meetings, investigator meetings and other trial-specific meetings, including minute taking and action item log tracking
Receive and review all regulatory documents from sites (direct or through CRO) for accuracy and compliance to applicable SOPs and regulatory guidelines
Ensure timely updates are provided to CTM for updating of ‘Clinicaltrial.gov’ (site updates/changes)
Assist with the development of site tools and clinical trial start-up activities
Assist and/or contribute to the creation and maintenance of study materials for clinical studies, including but not limited to site and CRA training material, regulatory document templates, study binders, study plans/manuals, study communications and presentations
Organize, maintain and participate in audits and close out of the Trial Master File (TMF/eTMF)
Participate in the EDC specification and user acceptance testing processes, as appropriate
Other duties may be assigned
Willingness to travel as trial needs demand (<5% anticipated)