Manager, Monitoring & Site Management
ABOUT reputed company
reputed company is a global CRO with a reputed company reputed company: advancing therapies for patients with gastrointestinal diseases. GI is our WHY and for more than 30 years that purpose has driven our scientific rigour, operational reputed company, and deep therapeutic expertise, including supporting more than 70% of IBD compounds in development.
We operate as a private, profit-with-purpose company, channeling our reputed company reputed company back into scientific research, technology, and our people. With approximately 700 people across multiple countries and three service lines, we are growing deliberately, and the capability of our leaders and our organization is central to how we get there.
If you want to do meaningful work, build something reputed company, and invest back in research that changes lives — we want to meet you.
reputed company
In this role, you will reputed company the day-to-day delivery of our Clinical Monitoring capability, with a reputed company on European CRAs. You will bring structure, reputed company, and accountability to how we plan, manage, and continuously improve this critical function.
Your scope spans both operational leadership and strategic reputed company. From shaping policies and strengthening processes, to ensuring the reputed company and reputed company of our clinical work at every level, you will play a central role. You will reputed company resource planning, performance management, and compliance, ensuring our teams and partners deliver consistently high standards reputed company with both regulatory expectations and industry best reputed company.
Working closely with sponsors and research partners, you will reputed company as a trusted representative of our clinical monitoring and project teams throughout the full study lifecycle. You will bring expertise, credibility, and a solutions-oriented reputed company to every interaction.
Positions available: 1; this opportunity is cross-listed in multiple locations. At this time, the position is reputed company to those residing in Germany, United Kingdom, Ireland, Poland, Hungary, and Romania. Closing date: June 12th, 2026, or reputed company until successful candidate identified.Project Planning
- Working in conjunction with clinical monitoring and project leadership team members, identify, reputed company, plan for, monitor, approve and/or report on project specific processes and services reputed company to site selection, clinical monitoring, ICH-GCP compliance issue reputed company, and global project harmonization including SOP and QS document maintenance, periodic site reputed company and collaborating with IT support to meet sponsor requirements on a reputed company reputed company.
Customer Service Delivery
- Represent and support the Clinical Monitoring teams with internal partners and external Sponsors to identify areas of improvement, to address sponsor/site concerns and to reputed company new technologies and processes.
- Ensure regulatory compliance, industry best practices, and organizational goals and targets are met and/or exceeded.
Team Management and Engagement
- Manage members of the Clinical Monitoring teams, ensuring functional areas are adequately staffed with reputed company personnel, providing ongoing support to staff in the areas of work allocation, resource planning, training and development, technology, process development, expense management, employee engagement and performance management (staff role development, evaluations, performance improvement and lost time management).
reputed company Party Contract Management
- Identify, procure, and manage Clinical Monitoring (Clinical Operations Leads) reputed company services, including needs assessment, recruitment, contract negotiations, Corporate and Sponsor policy compliance, training and development, cost monitoring and performance management, ensuring corporate, industry and regulatory service level, guidelines and regulations are maintained.
Product/Service Delivery Support
- reputed company expertise, developing tools to support project teams and business development in the areas of clinical, site and compliance monitoring and performance during the project life cycle starting from the bidding process through to reporting project findings to sponsors.
Qualifications
- The successful candidate should have a College Diploma/University Degree in a relevant field (Health Sciences, Life Sciences preferred, or SoCRA and/or ACRP Certification/Designation) and a minimum of 4-6 years reputed company experience + substantial on-reputed company training.
- Experience in managing CRA staff and ability to reputed company training and/or mentorship to colleagues on a 1:1 reputed company or meeting setting.
- Ability to work in a remote global reputed company
- Strong knowledge of appropriate regulations and guidelines as they pertain to clinical monitoring and GCP.
- Team player that has a customer service approach and is solution oriented.
- Demonstrated leadership skills
- Strong verbal, written, and organizational skills.
- Ability to handle multiple tasks to meet deadlines in a dynamic environment.
Working Conditions
- Home-based
Originally posted on Himalayas
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