Principal CTC

🔥 3 minutes ago

🇲🇽 Mexico – Remote

⏰ Full Time

🔴 Lead

✨ Principal

👻 Ghost score 15%

What it means: the chance that no one is really hiring for this job.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Thermo Fisher Scientific

WebsiteLinkedInAll Job Openings

10,000+ employees

🧬 Biotechnology

💊 Pharmaceuticals

🏥 Healthcare

Biotechnology • Pharmaceuticals • Healthcare

Thermo Fisher Scientific is the world leader in serving science, with a stated mission to enable customers to make the world healthier, cleaner and safer. The company provides a broad portfolio of laboratory instruments, analytical technologies, diagnostics, consumables, software and services that support life‑sciences research, analytical testing, clinical diagnostics and the development and manufacture of therapies. Its operations and offerings (as described on its site and in its news) include advanced imaging and electron microscopes, chromatography and mass‑spectrometry systems, genetic and clinical testing, lab automation and AI tools, bioprocessing and contract development/manufacturing services (brands cited include Thermo Scientific, Applied Biosystems, Invitrogen, Gibco, Fisher Scientific, Unity Lab Services, Patheon and PPD). Thermo Fisher reports annual revenue over $45 billion and emphasizes corporate social responsibility, environmental and community programs alongside its scientific products and services.

📋 Description

• Provide administrative and technical support to project teams as a study lead and cross-functional liaison • Coordinate and oversee assigned clinical trial activities, ensuring timely, budget-compliant, high-quality completion • Perform department, internal, country, investigator file, and eTMF reviews; document findings • Maintain study documentation, team lists, training trackers, system access, activity plans, databases, and vendor trackers • Support risk-based monitoring activities and audit readiness • Process and transmit documents to clients and centralized IRB/IEC • Schedule client and internal meetings and prepare meeting minutes • Review and track local regulatory documents and support submission activities • Analyze and reconcile study metrics and findings reports • Coordinate Investigator Site File, pharmacy binder materials, study supplies, and translation materials • Provide clinical trial system support, including Activate and eTMF • Train new personnel and other functional team members, investigators, and clients • Serve as an alliance-level lead for client integration and eTMF activities • Support site activation critical paths, site agreements, budgets, essential documents, feasibility, and regulatory compliance packages • Develop and maintain site lists, investigator contacts, site interest plans, survey data, and site communications • Conduct site interviews and provide local expertise on site capacity, experience, and tiering • Liaise with Global Investigator Services and contribute to global feasibility processes and best practices • Support clinical trial execution, stakeholder coordination, documentation, reporting, and operational continuity

🎯 Requirements

• High / Secondary school diploma or equivalent and relevant formal academic / vocational qualification • Previous experience providing the knowledge, skills, and abilities to perform the job, comparable to at least 6 years • Bachelor's degree preferred • Excellent English language and grammar skills and proficient local language skills as needed • Knowledge of applicable country regulations, ICH Good Clinical Practices, organization/client SOPs and WPDs • Proficiency in MS Office (Word, Excel, and PowerPoint) • Ability to master clinical trial database systems • Ability to successfully complete the organization's clinical training program • Excellent organizational, analytical, presentation, negotiation, oral and written communication, and problem-solving skills • Basic medical/therapeutic area and medical terminology knowledge • Basic knowledge of local health systems • Ability to work independently and in a matrix environment • Ability to manage risk and perform appropriate risk escalation • Secondary education in Business Administration or equivalent

🏖️ Benefits

• Fully remote work mode • Standard Monday–Friday work schedule • Potential occasional travel • Training and onboarding support • Professional development through clinical training and expanded therapeutic knowledge

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