Clinical Trial Coordinator

🔥 35 minutes ago

🇦🇷 Argentina – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

✨ Clinical Trial Coordinator

👻 Ghost score 10%

What it means: how likely this posting is sitting open without active hiring.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.

Apply Now

Find Similar Remote Jobs

Set Up Email Alert For New Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume

Thermo Fisher Scientific

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1956

🏥 Healthcare

📦 Logistics

🏭 Manufacturing

Healthcare • Logistics • Manufacturing

Thermo Fisher Scientific is the world leader in serving science, with annual revenue of more than $40 billion. Their mission is to enable customers to make the world healthier, cleaner, and safer by supporting life sciences research, solving complex analytical challenges, increasing laboratory productivity, and improving patient health through diagnostics and the development of life-changing therapies. With a global team, they offer innovative technologies and pharmaceutical services through brands such as Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD.

📋 Description

• Provide administrative and technical support to the Project Team • Coordinate and facilitate project activities and potentially serve as a study lead • Act as a cross-functional liaison for the project team • Support onboarding as a buddy and provide training to new staff as needed • Support departmental and cross-functional process improvement initiatives • Coordinate, oversee, and complete assigned trial activities according to the task matrix • Support department, internal, country, and investigator file reviews and document findings • Ensure allocated tasks are completed on time, within budget, and to quality standards • Communicate project risks to project leads and line manager • Maintain study documentation, team lists, training trackers, system access, and project activity plans • Keep the electronic Trial Master File up to date and provide GoBalto and eTMF system support • Process documents, perform eTMF reviews, conduct mass mailings, and provide reports to internal team members • Review and track local regulatory documents • Transmit documents to the client and centralized IRB/IEC • Analyze and reconcile study metrics and findings reports • Assist with resolving findings related to site documentation • Maintain vendor trackers • Coordinate, compile, and distribute Investigator Site File and Pharmacy binder materials and non-clinical study supplies • Assist with study-specific translation materials and translation quality control

🎯 Requirements

• High / Secondary school diploma or equivalent and relevant formal academic / vocational qualification • Bachelor's degree • Previous experience that provides the knowledge, skills, and abilities to perform the job preferred (comparable to at least 4 years) • Equivalent combination of appropriate education, training and/or directly related experience may be considered • Ability to work in a team or independently as required • Strong organizational skills and attention to detail, with ability to handle multiple tasks efficiently and effectively • Ability to analyze project-specific data/systems accurately and efficiently • Strong customer focus • Flexibility and adaptability to reprioritize workload and meet changing project timelines • Working knowledge of applicable Country Regulations, ICH Good Clinical Practices, and organization/Client SOPs and WPDs • Excellent English language and grammar skills and proficient local language skills as needed • Good presentation skills • Excellent computer skills; proficiency in MS Office (Word, Excel, and PowerPoint) • Ability to learn and master clinical trial database systems • Ability to successfully complete PPD clinical training program • Self-motivated, positive attitude with strong interpersonal skills

🏖️ Benefits

• Fully remote work arrangement • Standard Monday–Friday work schedule