Remote Senior Clinical Trials Leader

Kriya Therapeutics, Inc.; United States; Remoto; USD 130.000 - 190.000; Tempo pieno

Vantaggi offerti da questo lavoro

Flexible Time Off

Health Insurance

Equity

401(k) Matching

Life Insurance

Descrizione del lavoro

Kriya Therapeutics, Inc. is seeking a Senior Clinical Trial Manager to lead day-to-day operations of clinical trials, oversee CROs and vendors, and ensure trials meet ICH/GCP and SOP standards. This remote, US-based role requires strong cross-functional collaboration and budget stewardship.

Responsibilities include start-up activities, protocol input on operational aspects, and milestone reporting. Travel may be required to sites and conferences as needed.

Competenze

• Minimum 6+ years in pharma/biotech with 4+ years clinical trials management.
• Ophthalmology experience highly preferred.
• Experience managing external suppliers or virtual teams (CROs/independent contractors).
• Budget and contract negotiation experience.

Mansioni

• Oversee day-to-day management of clinical trials, vendors, and sites.
• Lead start-up, conduct, and close-out activities for studies.
• Develop study budgets and negotiate contracts with vendors.
• Create and amend informed consent forms and trial documents.
• Ensure compliance with SOPs, ICH/GCP and regulatory guidelines.
• Coordinate with CROs and external vendors for milestones and timelines.
• Provide regular study status updates to program management.

Conoscenze

Clinical Trials Management

Vendor Management

Budget Negotiation

EDC/CTMS/IRT

Cross-functional Leadership

Communication

Regulatory Knowledge

Independent Work

Formazione

BS or equivalent

Strumenti

EDC

CTMS

IRT

UAT

Descrizione del lavoro

Kriya Therapeutics, Inc. is seeking a Senior Clinical Trial Manager to lead day-to-day operations of clinical trials, oversee CROs and vendors, and ensure trials meet ICH/GCP and SOP standards. This remote, US-based role requires strong cross-functional collaboration and budget stewardship.

Responsibilities include start-up activities, protocol input on operational aspects, and milestone reporting. Travel may be required to sites and conferences as needed.