Clinical Documentation Specialist for Global Clinical Trials
hace 1 mes
At Fortrea, a leading global contract research organization (CRO), we're seeking a skilled Clinical Document Specialist to join our Clinical Pharmacology Services team. This exciting opportunity allows you to contribute to the development of life-changing therapies and treatments while working in a dynamic, remote environment.
The ideal candidate will be responsible for maintaining and archiving documents produced by study project teams within CPS, organizing and filing relevant documents into electronic and/or paper locations, and ensuring the Trial Master File (TMF) meets quality and integrity specifications. Additionally, they will work closely with Study Project Managers to review and finalize TMF plans and indexes, create tracking forms and spreadsheets, and maintain departmental files.
As a successful candidate, you will have experience working in an administrative or IT-focused role within clinical trials or a hospital/medical setting. You'll also possess strong written and verbal communication skills, organizational abilities, and proficiency in basic computer programs like Adobe Acrobat, Word, Excel, and PowerPoint. Full training will be provided to ensure your success in this role.
We offer a competitive salary of $60,000 - $80,000 per year, depending on experience, along with opportunities for growth and professional development in a supportive and inclusive work environment. As a proud equal opportunity employer, we value diversity and inclusion and strive to create a workplace where all employees feel empowered to grow and make a meaningful impact.
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Xico, México Worldwide Clinical Trials A tiempo completoAbout the RoleWe are seeking a skilled and detail-oriented Global Clinical Trials Operations Coordinator to join our team at Worldwide Clinical Trials. In this role, you will play a critical part in ensuring the smooth operation of our clinical trials.
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Clinical Trial Associate II, TMF Operations Specialist
hace 3 semanas
Xico, México Worldwide Clinical Trials A tiempo completoJob Title: Clinical Trial Associate II, TMF Operations SpecialistJob Summary:We are seeking a highly organized and detail-oriented Clinical Trial Associate II, TMF Operations Specialist to join our team at Worldwide Clinical Trials. In this role, you will be responsible for processing, maintaining, and archiving all essential documents in compliance with...
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Global Payments Coordinator
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Global Clinical Trials Coordinator Specialist
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Senior Legal Manager for Clinical Trials
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Xico, México Novo Nordisk A tiempo completoSenior Legal Manager for Clinical TrialsWe are seeking an experienced Senior Legal Manager to join our team at Novo Nordisk. As a key member of our Legal and Compliance department, you will play a crucial role in ensuring compliance with laws, regulations, and internal policies for clinical trials.About the Role:Ensure compliance with laws, regulations, and...
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Clinical Trials Operations Specialist
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Xico, México Pfizer A tiempo completoRole SummaryWe are seeking a skilled Clinical Trials Operations Specialist to join our team, responsible for the global site activation process. This role will ensure seamless execution of clinical trials by collaborating with investigators, sites, and internal stakeholders.About the JobThe ideal candidate will have a scientific or technical degree in...
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Clinical Document Specialist
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Xico, México Fortrea A tiempo completoJob TitleClinical Document SpecialistAbout the RoleWe are seeking a highly organized and detail-oriented Clinical Document Specialist to join our global Clinical Pharmacology Services team. As a Clinical Document Specialist, you will be responsible for maintaining and organizing clinical documents related to our projects, ensuring that all documentation is...
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Operations Coordinator for Clinical Trials
hace 4 semanas
Xico, México Thermo Fisher Scientific A tiempo completoAt Thermo Fisher Scientific, we are seeking a highly skilled Operations Coordinator to support our clinical trials team. This role is ideal for an individual who is detail-oriented, organized, and able to work effectively in a fast-paced environment.**Job Summary:**The Operations Coordinator will be responsible for coordinating and overseeing various tasks...
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Strategic Regulatory Expert for Clinical Trials
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Clinical Trials Senior Analyst
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Global Adverse Event Specialist
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Xico, México Worldwide Clinical Trials A tiempo completo**About Us**At Worldwide Clinical Trials, we're a global midsize Contract Research Organization (CRO) that pushes boundaries, innovates, and invents to find cures for the world's most persistent diseases.We believe everyone plays an important role in making a difference for patients and their caregivers. Our mission is to work with passion and purpose every...
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Clinical Trial Specialist
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Xico, México Thermo Fisher Scientific A tiempo completoJob Summary:We are seeking a Clinical Trial Specialist with expertise in regulatory compliance to join our team at Thermo Fisher Scientific. As a Clinical Trial Specialist, you will be responsible for ensuring the seamless execution of clinical trials while adhering to regulatory requirements and company standards.
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Clinical Trials Specialist
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Xico, México Icon Plc A tiempo completoContract Analyst I Job DescriptionAt Icon PlcWe are seeking a skilled Contract Analyst I to play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.Key Responsibilities:Review and analyze contracts, agreements, and legal documents related to...
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Accounts Receivable Expert
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Xico, México Worldwide Clinical Trials A tiempo completoJob DescriptionWe are seeking a highly skilled Associate, Accounts Receivable to join our team at Worldwide Clinical Trials.Job Summary:Prepare and render invoices to sponsors/clients for services, pass-through cost reimbursements, and grants.Maintain and reconcile billing, accounts receivable, and related reports.Reconcile unbilled services/reimbursable...
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Global Clinical Development Specialist
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Clinical Research Coordinator
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Principal Document Specialist
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