Clinical Risk Manager I

Premier Research Group; Argentina; Remote; ARS 2,400,000 - 4,200,000; Full time

Job summary

Premier Research is seeking a Clinical Risk Manager I to join our Clinical Management team. Remote role focused on RBQM, risk assessment, QA readiness and cross-functional collaboration. You will help biotech, medtech and pharma partners transform ideas into safe, effective medicines and devices.

Responsibilities include developing monitoring strategies, leading risk-based planning and ensuring documentation integrity across studies, with travel up to 20% when required.

Qualifications

• Bachelor in Biological Sciences or Health Sciences or related field.
• 8+ years in clinical research RBQM, central monitoring and project management.
• Subject matter expertise on ICH-GCP, ICH E6(R2+R3) and RBQM concepts.
• Experience with KRI, QTLs, QbD and central monitoring.
• Willingness to travel up to 20%.
• Excellent verbal and written English communication.

Responsibilities

• Support Bidder, Proposals and Business Development with monitoring strategy rationale.
• Lead RBM planning and risk assessment for studies and trials.
• Ensure inspection readiness and complete RBM documentation.
• Act as SME on Risk Management and RBM activities across studies.
• Collaborate with cross-functional teams to implement risk-based monitoring.

Skills

RBQM expertise

Data analysis

Excellent English

Education

Bachelor's in Biological Sciences/Health Sciences

Tools

MS Excel

Business Intelligence tools

Job description

## Clinical Risk Manager IApply: Remote: Argentina: Full time: Posted 11 Days Ago: R6950Premier Research is looking for a Clinical Risk Manager I to join our Clinical Management team.You will help biotech, medtech, and specialty pharma companies transform life-changing ideas and breakthrough science into new medicines, devices, and diagnostics. What we do is profoundly connected to saving and improving lives, and we recognize our team members are the most valuable asset in delivering success.* We are here to help you grow, to give you the skills and opportunities to excel at work with the flexibility and balance your life requires.* Your ideas influence the way we work, and your voice matters here.* As an essential part of our team, you help us deliver the medical innovation that patients are desperate for.Join us and build your future here.**What you'll be doing:*** Support Clinical Bidder, Proposals and Business Development by providing the rationale for the overarching monitoring strategy based on initial risk assessment, as needed.* Upon study award, completes the study RACT for complex and/or global trials, which includes identification of Critical Data and Critical Processes, as well as protocol execution risks and cross functional mitigative strategies for the identified risks, with study team input.* Evaluates whether Quality Tolerance Limits (QTLs) should be considered, and if so, leads discussion with required functions to establish initial QTL parameters.* Confirms the proposed custom monitoring strategy is fit for purpose and risk proportionate.* Ensures the Central Monitor, if in scope, has the required tools to perform aggregated data reviews via analytics, or other methods.* Creates configuration notes for programmers of Clinical Analytics.* Authors the Integrated Quality Risk Management Plan (IQRMP) for assigned studies.* Serves as a Subject Matter Expert (SME) on Risk Management and Risk Based Monitoring (RBM) activities for assigned studies.* Supports functional leads in completing functional project plans, ensuring relevant mitigations are captured as expected.* Supports ongoing cross-functional protocol execution risk reviews through the entire project life cycle.* Supports Kick Off meetings for new awards and opportunities.* Ensures inspection readiness related to Risk Management and RBM strategy by maintaining accurate and complete documentation.* Build knowledge of RBQM processes and share learnings within the team.**What we are searching for:*** Bachelors in Biological Sciences, Health Sciences and/or related disciplines in the health care domain.* Significant clinical research experience, 8+ years of related experience to RBQM, Central Monitoring and Project Management. Subject matter expertise on ICH-GCP, ICH E6 (R2 + R3) Guidelines and RACT tools, preferred.* Subject matter expertise on RBQM, KRI, QTLs, QbD, Centralized Monitoring, Budgeting and Contracts* Understands the key concepts of RBQM, Key Risk Indicators (KRI), Quality Tolerance Limits (QTLs), Quality by Design (QbD), Clinical, Centralized Monitoring and budget.* Excellent analytical, computational, judgement and decision-making ability* Strong fundamental understanding of statistical concepts, statistical analysis techniques and Integrated Quality Risk Management (IQRM) theories* Lead process improvement initiatives at department/organizational level* Expertise with MS Excel, Business Intelligence tools and leverages data visualizations for decision making.* Experience of collaborating with cross-functional global team for solving complex problem* Excellent verbal and written communication skills in English* Ability to travel up to 20% for sponsor meetings.### Why Choose Premier?* Premier Research is more than a company – it’s a community furthering research to improve the lives of patients in critical need. We are a diverse staff thinking creatively, challenging ideas, and solving complex problems.* Our Values – We Aim High, We Work Together, We Stay Agile, We Get It Done, We Care – mirror the determination, flexibility and trust that our team embodies.* As a Premier team member, you have the power to make an impact, regardless of job title and location.* Our dedication to biotech and specialty pharma is unlike any other.* We provide our staff with innovative technologies and continuous learning.