TFS HealthScience - Contract Research Organization
501 - 1000 employees
Founded 2007
💼 Consulting
🏥 Healthcare
📦 Logistics
Consulting • Healthcare • Logistics
TFS HealthScience is a leading global Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies to advance clinical development. They offer a wide range of solutions including phase I-III clinical development, real-world evidence (Phase IV) studies, and strategic resourcing solutions. TFS HealthScience specializes in multiple therapeutic areas such as dermatology, internal medicine, neuroscience, oncology and hematology, ophthalmology, pediatrics, rare diseases, and orphan drugs. They aim to bring treatments to patients faster by combining their full-service capabilities and global reach with the flexibility and personalized approach of a mid-size CRO.
Freelance Senior Clinical Research Associate
Job not on LinkedIn
🔥 0 minutes ago
📊 Check your resume score for this job
Improve your chances of getting an interview by checking your resume score before you apply.
TFS HealthScience - Contract Research Organization
501 - 1000 employees
Founded 2007
💼 Consulting
🏥 Healthcare
📦 Logistics
Consulting • Healthcare • Logistics
TFS HealthScience is a leading global Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies to advance clinical development. They offer a wide range of solutions including phase I-III clinical development, real-world evidence (Phase IV) studies, and strategic resourcing solutions. TFS HealthScience specializes in multiple therapeutic areas such as dermatology, internal medicine, neuroscience, oncology and hematology, ophthalmology, pediatrics, rare diseases, and orphan drugs. They aim to bring treatments to patients faster by combining their full-service capabilities and global reach with the flexibility and personalized approach of a mid-size CRO.
📋 Description
• Function operationally as a member of a Project Team during clinical study conduct • Initiate, monitor on-site and remotely, and close out study sites • Provide unmasked CRA support for assigned clinical studies • Manage investigational product accountability and oversee unblinded site activities • Monitor protocol compliance, subject safety, data integrity, and study quality • Verify informed consent procedures and protocol requirements • Review electronic or paper CRFs and source documentation • Report monitoring-visit actions, findings, and corrective/preventive actions • Escalate deficiencies and issues as appropriate • Provide sites with identified issues and required action items • Deliver site documents to the eTMF or paper TMF • Verify maintenance of Investigator Site Files • Update CTMS and other project systems with accurate site information • Participate in audit and inspection preparation and follow-up • Order, ship, and reconcile clinical investigative supplies when applicable • Assist Clinical Research or Project Managers with project tracking, monitoring plans, report review, and CRA resource management • Perform Assessment Site Visits when requested • Mentor CRAs and develop therapeutic-area training when needed • Participate in capabilities presentations • Collaborate with study teams, investigative sites, and sponsors to deliver study milestones on time while maintaining study blinding and data quality
🎯 Requirements
• Bachelor’s Degree, preferably in life science or nursing; or equivalent • More than 5 years of independent on-site monitoring experience required • At least 1 year of experience as an unmasked monitor required • At least 1 year of Ophthalmology experience preferred, ideally in a retina indication • Ability to work in a fast-paced environment with changing priorities • Understanding of basic medical terminology and science related to assigned drugs and therapeutic areas • Understanding of Good Clinical Practice regulations and ICH guidelines • Ability to work independently and in a team matrix organization • Excellent written and verbal communication skills • Fluency in English and the local language • Excellent organizational skills • Technology savvy with good software and computer skills • Self-awareness, resolve, flexibility, collaborative mindset, proactivity, analytical approach, and attention to detail • Coachability and motivation to take on new challenges • Ability to facilitate discussions and use diplomacy in difficult situations • Ability to take ownership of assigned tasks • Ability to manage complex or early-phase studies • Ability and willingness to travel up to 60–80%, including overnight and international travel if applicable
🏖️ Benefits
• Competitive compensation package • Comprehensive benefits • Opportunity for personal and professional growth • Collaborative and innovative environment • Opportunity to make a difference in the lives of patients
Apply Now
