TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service-capabilities, resourcing and Functional Service (FSP) solutions.

Join Our Team as a Clinical Research Manager (CRM)

About this role

As part of our Ohtalmology team you will working alongside passionate and innovative professionals to ensure our customers achieve their goals.

The Clinical Research Manager (CRM) is responsible for coordinating and overseeing country and site management activities throughout study conduct, ensuring high‑quality delivery in accordance with company SOPs, regulatory requirements, and contractual obligations.

Key Responsibilities: 

• Oversee day‑to‑day clinical operations to ensure delivery according to protocol, SOPs, ICH/GCP, and regulatory requirements.

• Serve as the primary operational contact for Sponsors, providing updates, managing expectations, and ensuring high‑quality study execution.

• Lead and support CRAs, including training, supervision, performance oversight, co‑monitoring, and review/approval of monitoring visit reports.

• Ensure site and country performance through proactive review of monitoring activities, protocol deviations, data listings, recruitment progress, and issue escalation.

• Maintain oversight of study documentation, including TMF quality, CTMS accuracy, monitoring plans, training plans, and study‑specific materials.

• Collaborate with the Project Manager on study planning, investigator payments, resource allocation, study communications, and revenue forecasting.

• Contribute to study meetings, Investigator Meetings, feasibility assessments, and, when required, local project management, CRA support, and bid defense activities.

Qualifications: 

• Minimum 5 years of clinical monitoring experience in a CRO, pharmaceutical, or biotechnology environment.

• At least 1 year of experience as a Clinical Research Manager (CRM) with proven oversight of site and country operations.

• 1+ years of experience in Ophthalmology (OPH), ideally within retina indications such as DME, AMD, GA, RVO, or inherited retinal diseases (IRDs).

• Fluency in Spanish and Portuguese is required.

• Strong understanding of ICH/GCP, regulatory requirements, and clinical operations processes.

• Demonstrated ability to lead CRAs, manage study deliverables, and collaborate effectively with cross‑functional teams.

What We Offer

We provide a competitive compensation package, comprehensive benefits and the opportunity for personal and professional growth in a rewarding environment. You’ll be joining a team that values collaboration, innovation, and making a difference in the lives of patients

A Bit More About Us

Our journey began over 30 years ago in Sweden, in the city of Lund. As a full-service, global Contract Research Organization (CRO), we build solution-driven teams working towards a healthier future. Bringing together over 600 professionals, TFS delivers tailored clinical research services in more than 50 countries with flexible clinical development and strategic resourcing solutions across key therapeutic areas including Dermatology, Neuroscience, Oncology and Ophthalmology.

Our core values of Trust, Quality, Passion, Flexibility, and Sustainability are our guiding light serving as the framework for decision-making at all levels of the organization. They assist us in attracting and retaining valuable talent who share our sentiments, resulting in high employee engagement and satisfaction. By aligning on these fundamental values, we cultivate a unified force, geared towards innovation and excellence. This collective effort propels us towards our shared goal and fosters a culture of mutual respect and collaboration. 

Together we make a difference.