Senior Clinical Trials Lead — Remote

Kriyatx; California; Remote; USD 140,000 - 190,000; Full time

Benefits offered by this job

Flexible Time Off

Medical, Dental, Vision Insurance

401(k) with company match

Equity

Job summary

Kriya Therapeutics, Inc. is seeking a Senior Clinical Trial Manager to oversee day-to-day operations of clinical trials, vendors, and sites. You will ensure adherence to SOPs and ICH/GCP guidelines while coordinating with cross-functional teams to meet timelines and budgets.

The role emphasizes managing CROs, trial documentation, and study milestones in a fast-paced, remote environment. Travel may be required, with strong focus on ophthalmology and gene-therapy trials.

Qualifications

• BS or equivalent required.
• Minimum 6+ years in pharma/biotech with at least 4 years in clinical trials management.
• Ophthalmology experience preferred.
• Experience managing external suppliers and/or working in a virtual environment.
• Budget and contract negotiation experience.
• Knowledge of ICH/GCP and GxP guidelines.
• Proficient with EDC, CTMS, IRT; strong communication skills.
• Willing and able to travel (domestic and international).

Responsibilities

• Oversee day-to-day management of clinical trials, vendors, and sites.
• Support study budgets, vendor contracts, and invoice review.
• Lead start-up, conduct, and close-out activities.
• Assist in protocol development related to operational trial aspects.
• Serve as primary contact for CROs and vendors on studies.
• Create and update informed consent forms and trial documents.
• Track milestones and timelines; report status to management.
• Participate in CRO/vendor selection and partnership development.
• Collaborate with QA to stay compliant with local regulations.

Skills

Clinical trial management

Vendor management

Leadership

Communication

Time management

Education

BS or equivalent

Tools

EDC

CTMS

IRT systems

UAT

Job description

Kriya Therapeutics, Inc. is seeking a Senior Clinical Trial Manager to oversee day-to-day operations of clinical trials, vendors, and sites. You will ensure adherence to SOPs and ICH/GCP guidelines while coordinating with cross-functional teams to meet timelines and budgets.

The role emphasizes managing CROs, trial documentation, and study milestones in a fast-paced, remote environment. Travel may be required, with strong focus on ophthalmology and gene-therapy trials.