Senior Performance Marketing Strategist
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Lead paid media strategy across Google, LinkedIn, Meta, and Microsoft for growing B2B companies. Connect campaign investment to pipeline and revenue through strategic client leadership.
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Thermo Fisher Scientific ऐसी प्रौद्योगिकियाँ, प्रयोगशाला उत्पाद और फार्मास्युटिकल सेवाएँ विकसित तथा उपलब्ध कराती है, जो वैज्ञानिक अनुसंधान और स्वास्थ्य सेवा को समर्थन देती हैं। इसका कार्य जीवन विज्ञान अनुसंधान, विश्लेषणात्मक समस्याओं के समाधान, प्रयोगशाला उत्पादकता, निदान तथा उपचारों के विकास और निर्माण तक फैला हुआ है। कंपनी Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon और PPD सहित विभिन्न ब्रांडों के पोर्टफोलियो तथा एक वैश्विक टीम के माध्यम से ग्राहकों की सेवा करती है। इसके करियर अवसर इन उत्पादों और सेवाओं से जुड़ी वैज्ञानिक, स्वास्थ्य सेवा, विनिर्माण, लॉजिस्टिक्स और सेवा संचालन को शामिल करते हैं।
Remote Clinical Trial Coordinator in Argentina
Support clinical trial site activation, regulatory documentation, feasibility work, and site communications for a global clinical research organization. Maintain trial systems, study files, metrics, and investigator site materials.
विवरण
- Coordinate assigned clinical trial activities in line with the task matrix
- Review departmental, internal, country, and investigator files and document findings
- Deliver assigned work on schedule, within budget, and to required quality standards
- Support Activate and eTMF systems while keeping study databases up to date
- Process Client (e)TMF documents, complete reviews, distribute communications, and prepare reports
- Analyze and reconcile study metrics and findings reports
- Coordinate and distribute Investigator Site File materials, pharmacy binders, and study supplies
- Support translation materials and perform translation quality checks
- Stay current on SOPs, client instructions, and applicable regulatory guidance
- Assist with client and internal meeting coordination, regulatory tracking, and RBM activities
- Maintain study records, training logs, system access, team lists, and activity plans
- Submit documents to clients and centralized IRB/IEC bodies
- Maintain vendor trackers and assist with regulatory submissions
- Work with sites to collect site-selection documentation
- Assemble regulatory compliance review packages
- Coordinate with internal teams to align site start-up activities
- Complete Site Interest Plans and collect site documentation when required
- Record site communications, follow-ups, and survey responses in real time
- Check survey data for logical consistency, completeness, and accuracy
- Work with teammates and clinical staff to address site issues and risks
- Monitor site-contact plans and escalate concerns or non-compliance
- Apply local knowledge of site capacity and experience to recommend additional sites
- Partner with Global Investigator Services to resolve investigator questions and maintain contact details
- Contribute to global feasibility workflows and continuous improvement practices
- Train new team members on relevant processes and systems
- Use local market knowledge to identify and develop new clinical trial sites
आवश्यकताएँ
- High school or secondary diploma, or equivalent, plus relevant academic or vocational training
- Comparable professional experience of 0–1 year
- Bachelor’s degree preferred
- Strong English communication and grammar skills, with local-language proficiency where required
- Proficiency with Microsoft Word, Excel, and PowerPoint
- Capacity to learn and use clinical trial database systems
- Working knowledge of applicable country regulations, ICH Good Clinical Practice, and organizational or client SOPs and WPDs
- Ability to complete the organization’s clinical training program successfully
- Accuracy in following project work instructions
- Ability to identify risks and escalate them appropriately
- Occasional driving to site locations and potential occasional travel required
लाभ
- Fully remote work arrangement
- Full-time employment
- Standard Monday–Friday schedule
- Potential occasional travel
- Training and onboarding support
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