Clinical Quality Specialist Full Time

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, ENCELTO TM (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.

Job Requirements

• 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

Education & Experience

• 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

Neurotech Pharmaceuticals provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.