Assistant CRA

🔥 26 minutes ago

🇧🇷 Brazil – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

🧪 Clinical Research

👻 Ghost score 12%

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.

Apply Now

Find Similar Remote Jobs

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

• Perform remote activities on assigned clinical research projects in liaison with the CRA and study Clinical Lead • Support site preparedness and the logistics of the monitoring process • Assist with site management and remote monitoring tasks in accordance with SOPs and regulatory guidelines • Complete study and site management activities defined in the task matrix • Complete and document study-specific training and orientation on study systems • Provide in-house support during pre-study assessments and assessment waivers • Customize site informed consent forms with site contact details as needed • Perform remote review of EMR/EHR checklists and support applicable assessments • Verify document collection and RCR submission status; update site EDL and verify site information • Review patient-facing materials and translations • Support vendor qualification processes and site staff system access • Follow up on site staff training • Coordinate logistics for investigator meeting attendance • Maintain vendor trackers and coordinate study/site supplies • Collect, review, and update essential documents in applicable systems • Follow up on missing vendor data, including ECGs, lab samples, and e-diaries • Support ongoing remote review of centralized monitoring tools • Support site payment processes, system updates, reconciliations, and invoice follow-up • Perform reconciliation tasks involving CRF and query status, deviations, SAEs, and safety reports • Verify document collection status and follow up on missing, incomplete, expired, or open documents • Perform other assigned site management tasks and possible FSP role profiles • Complete administrative tasks such as expense reports and timesheets

🎯 Requirements

• Bachelor's degree in a life science discipline or related field, or Registered Nursing certification or equivalent and relevant formal academic/vocational qualification • Previous experience providing the knowledge, skills, and abilities to perform the job, comparable to 0–2 years • Equivalency through a combination of appropriate education, training, and/or directly related experience may be considered • Basic medical/therapeutic area knowledge and understanding of medical terminology • Ability to attain and maintain working knowledge of ICH GCP, applicable regulations, and company procedural documents • Effective oral and written communication skills • Excellent interpersonal and customer service skills • Good organizational and time management skills, with strong attention to detail and ability to handle multiple tasks efficiently • Flexibility and adaptability • Ability to work independently or in a team • Well-developed critical thinking, root cause analysis, and problem-solving skills • Proficient computer skills and good knowledge of Microsoft Office; ability to learn and use appropriate software • Ability to extract pertinent information from study documents, electronic study data systems, CTMS, and dashboards • Excellent English language and grammar skills

🏖️ Benefits

• Fully remote work arrangement • Standard Monday–Friday work schedule • Occasional travel to clinics/hospitals may be required • Opportunity for career progression into CRA roles, which may include direct promotional opportunities • Exposure to global clinical research projects across 100+ countries

📊 Check your resume score for this job

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

Upload Resume