Clinical Team Lead II (Remote, Poland)

Overview

Join us in redefining what it means to work for a CRO. Working at Rho, you’ll be joining a team who take healthcare and clinical research personally, with shared experiences that drive a passion to heal, cure and solve some of humanity’s biggest challenges.

At Rho, we’re committed to you just as you’re committed to us. You’ll have the opportunity to experience a thriving company with real stability - financial, workforce, and corporate, which has created a safe environment to innovate and develop over a long and rewarding career. With a collaborative team of smart, talented, and positive people, you’ll be celebrated and respected for your expertise and given the freedom to think creatively, challenge the norm, and problem-solve.

We are currently hiring a Clinical Team Lead II to join our team! The Clinical Team Lead is integral to driving project success. In this role, you will have the opportunity to independently manage and lead the clinical team on select projects. You’ll provide direction to and train CRAs assigned to those projects. In addition, you’ll be responsible for the oversight of all operational aspects related to the planning and management of CRA and site performance. You’ll ensure that sites and CRAs operate in compliance with study protocols, ICH / GCP guidelines, and local Regulations.

Our Clinical Operations Team will tell you, joining Rho has been one of their best career moves in terms of contentment, financial rewards and career growth, which is why we have such stability in the group!

Responsibilities

• Proactively drive project success, including working closely with Project Managers to develop and implement enrollment strategies
• Responsible for operational aspects of planning and management of site performance in accordance with departmental productivity expectations
• Develop monitoring tools and plans
• Determine and drive the study start up process (track and report progress, review data), ensuring that all sites are selected and supplies provided in accordance with study start expectations
• Provide skilled review of study protocols and other study materials (e.g. CRF)
• Monitor clinical operations timelines, metrics, resourcing, budget and activities
• Provide status updates to project management and sponsors
• Lead regular clinical team teleconferences
• Work effectively with Site Study Coordinators
• Participate in the RFP process, including internal and external business development meetings
• Review monitoring visit reports and ensure finalization is within contractual timeline
• May assist Project Managers with project management tasks as assigned
• Create and conduct training sessions including investigator meetings, conferences, and team trainings
• Support the management and development of other CRAs
• Participate in the Clinical Operations community at Rho by leading key internal initiatives and standard operating procedures for the administration and monitoring the clinical trials

Qualifications

A few more things to know about us :

Benefits : Rho provides a comprehensive benefits package for all benefit-eligible employees, which includes medical, vision, dental, HSA, FSA, EAP, life & disability insurance and 401(k). All employees are eligible for paid time off, holidays, parental leave and bereavement leave.

Flexibility : We encourage a work-life balance that allows employees to bring their best selves to work while being passionate about their lives outside work.

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