Clinical Quality Specialist

NEUROTECH U S A

2d•Remote

About The Position

Neurotech Pharmaceuticals, Inc. is a private biotech company located in Cumberland, RI and Needham, MA, within the realm of Greater Boston’s vast biotechnology landscape. Since our inception more than 20 years ago, our focus has been on developing and commercializing transformative therapies for chronic eye diseases. The core platform technology, Encapsulated Cell Therapy (ECT), is a first-in-class drug delivery platform designed to slow the progression of chronic eye diseases. Neurotech’s first commercial product, ENCELTOTM (revakinagene taroretcel-lwey), is approved in the United States for the treatment of adults with idiopathic Macular Telangiectasia Type 2 (MacTel). Encapsulated cell-based gene therapy is designed to provide long-term, sustained delivery of therapeutic proteins for the treatment of chronic eye diseases. The Clinical Quality Specialist provides hands-on support to the Clinical Quality function and broader Clinical Operations team to ensure compliance with Good Clinical Practice (GCP), internal procedures, and applicable regulatory requirements. This role partners closely with the Director of Clinical Quality to support the maintenance and continuous improvement of the Quality Management System (QMS), execution of the clinical audit program, and development of clinical SOPs and training initiatives. This is a mid-level role requiring prior clinical trial experience and the ability to operate independently with strong organization, sound judgment, and attention to detail. This is a remote position.

Requirements

Bachelor's degree in a relevant scientific discipline preferred
Minimum 2 years of clinical trial experience
Experience in sponsor, CRO, or site environment preferred
Exposure to QMS, audits, or SOP development is a plus
Working knowledge of GCP and clinical trial processes
Strong organizational and multitasking abilities
High attention to detail and quality
Sound judgment and problem-solving skills
Proficiency in Microsoft Office (Excel, Word, PowerPoint)
Familiarity with CTMS, eTMF, or eQMS systems preferred
Ability and willingness for approximately up to 10% domestic travel and consistent with department needs

Responsibilities

Support the maintenance and continuous improvement of the Clinical Quality Management System (QMS)
Assist with SOP creation, revision, formatting, and document lifecycle management
Track and support CAPA development, follow-up, and closure activities
Assist in planning and execution of internal and external audits
Support audit documentation and inspection readiness activities
Partner with Clinical Operations to ensure quality oversight across clinical trials
Support development of clinical processes, tools, and study documentation
Assist with development and delivery of training materials
Utilize systems such as eQMS, CTMS, and eTMF platforms
Ensure accurate tracking and documentation within applicable systems