Clinical Research Manager

About This RoleTFS 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 Provider (FSP) solutions.The Clinical Research Manager (CRM) is responsible for overseeing and monitoring clinical trial sites to ensure studies are conducted in accordance with protocol, Good Clinical Practice (GCP), ICH guidelines, and applicable regulatory requirements. The CRM will support study sites throughout the clinical trial lifecycle including initiation, monitoring, and close-out activities.As part of our SRS team, you will be dedicated to one sponsor, a global pharmaceutical or biotechnology company that is an industry leader within its therapeutic area.Key ResponsibilitiesConduct on-site and remote monitoring visits including site initiation, routine monitoring, and close-out visitsEnsure clinical trials are conducted according to protocol, GCP, ICH guidelines, and applicable regulatory requirementsReview source documentation and Case Report Forms (CRFs) to ensure accuracy, completeness, and data integrityEnsure the safety and rights of study participants through proper informed consent procedures and protocol complianceVerify proper management, storage, and accountability of Investigational ProductsPrepare and submit monitoring visit reports and follow up on identified issues and action items with study sitesMaintain study documentation including Investigator Site Files and ensure timely submission to eTMFUpdate CTMS and other project systems with accurate site-level informationSupport audit and inspection readiness activities when requiredQualificationsBachelor's degree in Life Sciences, Nursing, or a related field or equivalent experienceBackground in Dermatology and/or Immunology is requiredAt least 1 year of clinical research experience as a CRA, CRM, or similar roleExperience working with clinical trial sites in South America and/or Latin America is requiredGood understanding of GCP, ICH guidelines, and clinical trial processesExperience with on-site or remote monitoring activities is preferredStrong attention to detail and organizational skillsAbility to work independently and within a cross-functional team environmentStrong communication and problem-solving skillsFluent in English and Spanish (Spanish is required)What We OfferWe provide opportunities for personal and professional growth in a rewarding environment. You will join a team that values collaboration, quality, and making a difference in the lives of patients.Our core values of Trust, Quality, Passion, Flexibility, and Sustainability guide our decisions and shape our culture. By aligning on these values, we foster collaboration, innovation, and a shared commitment to excellence. Together, we make a difference.A Bit More About UsOur journey began over 30 years ago in Sweden, in the city of Lund. As a full-service global CRO, we build solution-driven teams working toward a healthier future. Bringing together over 600 professionals, TFS delivers tailored clinical research services in more than 50 countries, offering flexible clinical development and strategic resourcing solutions across key therapeutic areas including Dermatology, Neuroscience, Oncology, and Ophthalmology.TFS HealthScience is a global, mid-sized contract research organization (CRO) partnering with biotechnology and pharmaceutical companies across the full clinical development lifecycle. Our expertise spans full-service clinical development, project-based support, strategic resourcing, and Functional Service Provider (FSP) solutions, matching experienced professionals to roles where they deliver the greatest impact.