Senior Central Monitor (Remote)

ProPharma Group; Northern (KY); Hybrid; USD 90,000 - 120,000; Full time

Job summary

ProPharma Group is seeking a Senior Central Monitor (Remote) to support clinical monitoring teams through centralized data and reporting tools in line with SOPs, regulatory requirements, ICH and GCP guidelines.

You will perform remote site monitoring, support study strategies, and help track recruitment, enrollment, drug supply, and site payments, while communicating with site institutions and contributing to risk assessments and data reviews.

Qualifications

• Bachelor’s degree preferred; comparable training/experience considered.
• Minimum 3 years of experience in study coordination and/or in-house monitoring.
• Experience in biotechnology or pharmaceutical regulated environments is desirable.
• Familiarity with RBQM systems (e.g., Cluepoints) is a plus.
• Understanding FDA/ICH GCP guidelines and SOPs.

Responsibilities

• Perform remote site monitoring and management activities per FDA/local regulations and ICH GCPs.
• Support study monitoring teams to implement strategies, processes, and standards to ensure quality and on-time delivery.
• Assist data collection and generate reports on recruitment, enrollment, drug supply status, site payments, and tracking.
• Support data risk assessments and monitoring activities across the study.
• Coordinate with clinical site institutions and assist with document collection, visit prep, and data review as needed.

Skills

Effective communication

Prioritization

Cross-functional collaboration

Attention to detail

Education

Bachelor’s degree preferred

Tools

Electronic Document Management Systems

Electronic Data Capture Systems

Clinical Trial Management Systems

Job description

## Senior Central Monitor (Remote)Apply: United States: Full time: Posted Today: JR 10613For the past 25 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-profile drug and device programs.The Central Monitoring Associate position is responsible for providing support to the clinical monitoring teams while utilizing centralized data and reporting tools in accordance with Standard Operating Procedures (SOPs), Regulatory requirements, ICH and GCP guidelines and study specific plans.**Essential Functions:*** Performs remote site monitoring and management activities for assigned project(s) in accordance with FDA and/or local regulations and guidelines, ICH GCPs and ProPharma Group SOPs and project plans.* Supports study monitoring team in implementing study strategies, initiatives, and processes and standards, to ensure consistent, efficient, and quality processes to meet quality, and study delivery within the expected timelines.* Supports collection of data, and report generation to support activities such as recruitment plan, and enrollment, drug supply status, site payment status, and any other relevant tracking to support successful clinical trial execution.* Supports data risk assessments as assigned.* Supports monitoring teams throughout the duration of the study including communication with the clinical site institutions as appropriate.* May be required to support any document collection, visit preparation, and study data review and central monitoring activities as assigned.* Other duties as assigned.**Necessary Skills and Abilities:*** Effective communication, and interpersonal skills with ability to partner with cross functional internal and external stakeholders.* Must be able to prioritize multiple tasks, plan proactively, and accomplish goals using well-defined instructions and procedures.* Ability to contribute to the development of tools and processes that increase measured efficiencies of the project.* Proficiency in working with systems used in the clinical trial execution such as but not limited to Electronic Document Management Systems, Electronic Data Capture Systems, Clinical Trial Management Systems, etc.* Exhibits a good understanding of general quality assurance concepts and practices.* Highly organized with a strong attention to detail.**Educational Requirements:*** Bachelor’s degree preferred. Persons without a formal degree who have comparable depth and breadth of training and experience and who meet job-specific criteria are eligible for consideration.**Experience Requirements:*** Minimum 3 years of experience in study coordination and in house monitoring, or relevant work experience in the Biotechnology or Pharmaceutical industries or relevant, regulated environment.**Experience Desired:*** Working knowledge of Cluepoints RBQM System* Long-haul COVID/Pulmonary experience#LI-AP1#LI-REMOTEWe celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed.All applications to roles at ProPharma are personally reviewed by a member of our recruitment team. We do not rely on AI screening tools to support our hiring process. You will always receive an outcome to your application so that you have an answer from us - whether you're successful or not.Whilst ProPharma supports remote working, we also recognise the value that comes from in person collaboration. As such, we encourage any new hires that are based within a reasonably short commute of one of our offices to work on a hybrid basis and spend some time working from that office location, as agreed with your manager. All applications will be treated on their own merit and candidates will not be at any advantage or disadvantage based on their proximity to an office.