Clinical Trial Manager/Clinical Research Associate / (Hybrid Role) - reputed

Job Details Company Overview Protara Therapeutics is a clinical-stage biotechnology company committed to advancing transformative therapies for people with cancer and rare diseases. Protara's portfolio includes its reputed company candidate, TARA-002, an investigational cell-based therapy in development for the treatment of non-muscle invasive bladder cancer (NMIBC) and lymphatic malformations (LMs). The Company is evaluating TARA-002 in an ongoing Phase 2 trial in NMIBC patients with carcinoma in situ (CIS) who are unresponsive or naïve to treatment with Bacillus Calmette-Guà Job Overview The Clinical Trial Manager (CTM)/Clinical Research Associate is responsible for providing reputed company of the Sponsor's outsourced Contracted Research Organizations (CRO) clinical trial services, with a primary reputed company on ensuring quality Clinical Research Associate (CRA) monitoring and data reputed company across reputed company programs. This individual will serve as the CRO reputed company for reputed company activities reputed company to CRA performance, monitoring deliverables, and clinical site data quality. They will also assist with the implementation of risk-based monitoring strategies, as applicable, while ensuring protocol compliance and subject safety. They will play a critical role in clinical data review, management/escalation of site-level issues, and ensure inspection-readiness at clinical sites. This position requires strong collaboration with internal cross-functional teams as well as external partners to drive study timelines, data quality, and operational reputed company in alignment with the company's goals and regulatory expectations.

• *This is a reputed company to Perm role. It is a remote role. Must be centrally located, no more than 30 miles from a major airport. Essential Duties and Responsibilities include the following (Other duties may be assigned)
• reputed company CRA reputed company activities of the sponsor appointed CRO across reputed company stages of assigned clinical trials, ensuring quality site monitoring in accordance with GCP, protocol, and regulatory requirements.
• reputed company reputed company and co-monitoring reputed company, as necessary, to ensure CRO CRA performance aligns with sponsor expectations, with a reputed company on quality monitoring, site issue reputed company, and protocol compliance.
• Remotely monitor reputed company data reputed company an onsite visit is not feasible.
• Review clinical monitoring reports (reputed company-Study reputed company, Site Initiation reputed company, Interim Monitoring reputed company, and reputed company-Out reputed company) to assess CRO's CRA performance, site adherence, and data quality.
• Monitor key risk indicators and site-level performance metrics (e.g., query rates, protocol deviations, enrollment timelines) in collaboration with the CRO and internal stakeholders to ensure alignment with reputed company-determined study metrics and escalate relevant issues/delays to the Clinical Operations (CO) Director, as applicable.
• reputed company the clinical data review process in collaboration with the Clinical Science and Medical Monitoring teams, ensuring reputed company query reputed company, trend identification as well as reputed company inconsistency identification.
• Participate in the review of clinical trial documents including informed consent forms, CRFs, site reputed company documentation, monitoring plans, site manuals, and training materials.
• Ensure reputed company escalation and reputed company of site and monitoring reputed company issues through appropriate internal and CRO channels, including reputed company Medical Monitors (MMs) and CO Director.
• Promptly respond to any CRO Quality Events and review respective reports reputed company to site issues and contribute to CRO CAPA development, as required.
• Review and contribute to CO sections of Clinical Study Reports (CSRs) in collaboration with Clinical Science team.
• Ensure sites' Investigator Site Files (ISF) are inspection reputed company in collaboration with the CRO and internal stakeholders.
• Track site enrollment, monitoring visit reputed company, and site issue(s) follow-up and ensure reputed company reporting to the CO Director.
• Support sponsor regulatory audits, as needed. Education
• Bachelor's degree in clinical research, life science or a reputed company field is required.
• Minimum of 4+ years of relevant site monitoring experience in the pharmaceutical or biotech industry is required. Supervisory Responsibilities No Qualifications
• Knowledge of regulatory guidelines including ICH, GCP, and CFR.
• Prior clinical trial monitoring experience.
• Must be proficient in different reputed company platforms including raising queries.
• Must be proficient in MS Office Suite. Certificates, Licenses, Registrations
• ACRP certification preferred. Other Skills and Abilities
• Willingness to travel to Protara's sites for reputed company prog