Assistant CRA FSP

🕒 August 21

🇹🇷 Turkey – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧪 Clinical Research

👻 Ghost score 46%

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.Why this score:

• Open for 82 days.
• Jobs at this company usually fill in 25 days.
• Reposted once.
• No salary listed.

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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

• Complete study and site management activities according to task matrices and study direction • Complete and document study-specific training • Orient and train on study-specific systems • Provide in-house support for pre-study assessments and waivers • Customize site informed consent forms with site contact details as needed • Perform remote EMR/EHR checklist reviews and support applicable assessments • Verify document collection and regulatory content review submission status; update site EDL and verify site information • Review patient-facing materials and translations • Support vendor qualification processes for site staff • Coordinate system access for relevant site staff • Follow up on site staff training • Coordinate logistics for investigator meeting attendance • Maintain vendor trackers • Coordinate study and site supply management • Support essential document collection, review, and system updates • 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 trial reconciliation tasks, including CRF and query status, deviations, SAEs, and safety reports • Verify document collection status and drive action on missing, incomplete, or expired documents • Perform other assigned site management tasks under CRA direction • Perform client-requested 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 relevant formal academic/vocational qualification • Equivalent combination of appropriate education, training, and/or directly related experience may be considered • 0 to 2 years of comparable experience • Basic medical/therapeutic area knowledge and medical terminology • 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, attention to detail, and ability to handle multiple tasks • Flexibility and adaptability • Ability to work independently or in a team • Critical thinking, root cause analysis, and problem-solving skills • Proficient computer skills and good knowledge of MS Office • Ability to learn and use appropriate software and leverage modern technology • Ability to extract information from study documents, electronic study data systems, CTMS, and dashboards • Excellent English and Turkish language and grammar skills • Occasional travel to clinics/hospitals may be required • Must be able to meet frequent travel requirements of 60–80% for future CRA career-track opportunities

🏖️ Benefits

• Fully remote work arrangement • Standard Monday–Friday work schedule • Home office environment • Occasional travel to clinics/hospitals may be required • Career-track promotional opportunities

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