The Clinical Monitoring Oversight Manager (contractor) will provide oversight of trial monitoring activities to ensure data quality and patient safety in accordance to GCP and ICH guidelines, local regulations, and applicable SOPs.
The Clinical Monitoring Oversight Manager will work with Clinical Operations Leadership Team to develop necessary procedures and tools to support Clinical Trial Managers with drafting, implementation and review of monitoring plans, identifying monitoring performance issues, managing site quality matters, assessing data quality metrics, documenting potential risks, escalating appropriate risks and issues, and communicating necessary action plans with cross functional Study Management Team.
The Clinical Monitoring Oversight Manager will also conduct oversight monitoring visits, train Clinical Trial Managers to perform oversight monitoring visits, and identify appropriate methods/ processes for conducting oversight monitoring visits globally.
This position is remote or if in bay area in-house/hybrid.
They will report to a member of the Clinical Operations Leadership Team.
Responsibilities
Quality oversight of clinical monitoring activities by CROs and clinical trial conduct by Investigators and their clinical trial staff
Serve as an escalation point for clinical monitoring issues for Arcus Clinical Trial Managers and provide guidance or coaching, when necessary
Lead the completion of quality oversight tasks such as quality oversight visits, site visit report reviews, and the review and analysis of defined quality measures
Work with Arcus Clinical Trial Managers or CRO management staff in resolving and escalating (when necessary) quality issues identified during the conduct of oversight monitoring activities
Conducting or participating in oversight Monitoring visits
Identify, develop, improve, and implement the necessary procedures and documentation for quality oversight activities
Train newly onboarded team members to Arcus oversight monitoring and provide ongoing training as identified
Maintain oversight of established monitoring metrics and communicate to cross functional Study Management Team in support of trial execution
Escalate identified risks appropriately and timely
Participate and support in audits and inspections.
Respond and assist in CAPA/ Process Improvements as a result of audit and/ or inspections
Evaluate the quality and integrity of site practices, escalating quality and/or GCP issues with investigators and internal team as appropriate
Mentors junior staff
Conduct site engagement visits as needed
Requirements
Bachelor’s degree, preferably in a scientific field
Minimum 7 years of related industry experience in the pharmaceutical industry or equivalent, Minimum of 5 years of monitoring experience, with at least 1 year of oversight monitoring, preferably in oncology
Demonstrates core understanding of full life cycle of clinical trial activities
Excellent communication skills both verbal and written are required
Thorough understanding of ICH GCP guidelines
Excellent understanding of Risk-Based Monitoring and Quality Management Principles
Ability to establish priorities, sense of urgency and collaborate (interpersonal, relationship management) with the study team, cross functional team members and external partners/vendors and clinical trial sites
Excellent planning and organization skills
Self-motivated, assertive, and able to function independently and as part of a team
Strong interpersonal and negotiation skills as well as strong verbal and written communication (including presentation of materials to internal teams and external partners)
Proven problem solving and decision-making skills
Excellent IT Microsoft skills and experience using clinical trial management web-based systems (i.
e.
EDC, IRT, CTMS, eTMF, etc)
Ability and willingness to travel approximately 50% of the time (domestic and international), may vary depending on trial needs
Arcus Biosciences is an Equal Opportunity Employer and prohibits discrimination and harassment of any kind.
Arcus is committed to the principle of equal employment opportunity for all employees and does not discriminate based on race, religion, color, sex, gender identify, sexual orientation, age, non-disqualifying physical or mental disability, national origin, veteran status or any other legally protected status.
EOE/AA/Vets