Nabídky práce czech remote v lokalitě Home Office
Zobrazit podobné nabídky práce u tohoto zaměstnavateleThermo Fisher Scientific3,4Home OfficeReklama·- Conduct remote or on-site visits to assess protocol and regulatory compliance and manage necessary documentation.
- A Day in the Life.
- Productive PlayhouseHome Office·
- Benefits: Flexible schedule, work from home.
- Please note, the pay rate are in US dollars and payment will be made in US dollars.
- Crypto.comHome Office·
- Flexi-work hour and hybrid or remote set-up.
- Weekly workload is 2-10 hours per week.
- Translate/ Review UI, marketing materials, help articles and research…
Zobrazit podobné nabídky práce u tohoto zaměstnavateleFoxelli GroupHome Office·- Full flexibility with your schedule in a fully remote setting for your control of a working day, powered by Hubstaff for transparency and fairness.
- Foxelli GroupHome Office·
- Full flexibility with your schedule in a fully remote setting for your control of a working day, powered by Hubstaff for transparency and fairness.
- Foxelli GroupHome Office·
- Full flexibility with your schedule in a fully remote setting for your control of a working day, powered by Hubstaff for transparency and fairness.
- VF CorporationHome Office·
- Office Prague, Czech or Warsaw, Poland (hybrid/remote).
- The HRIS Specialist will be responsible for ensuring the system is updated and functional, analyzing…
- WYR, s.r.o.Home Office·
- 40 000 Kč / měsíc nebo si řekni o víc.
- Znalost PHP (nebo jiného jazyka).
- Plat podle zkušeností 25-40 tis. junior,.
- Mzda 20 000 - 40 000 Kč / měsíc.
Zobrazit podobné nabídky práce u tohoto zaměstnavateleFoxelli GroupHome Office·- Full flexibility with your schedule in a fully remote setting for your control of a working day, powered by Hubstaff for transparency and fairness.
- ViatrisHome Office·
- Access – Providing high quality trusted medicines regardless of geography or circumstance;
- Pravidelný reporting aktivit v terénu v interním CRM systému.
- Agentura Parole s. r. o.Home Office·
- Agentura Parole s. r. o.
- CZK 30,000 - 40,000 • Part-time • Remote work - EU.
- We are looking for native speakers of English.
- Full-time/part-time schedule.
- DEVIX TechnologiesHome Office·
- You will be working on projects involving real-time sports data, interactive content, and video-on-demand platforms, ensuring a seamless experience for…
Zobrazit podobné nabídky práce u tohoto zaměstnavateleFoxelli GroupHome Office·- Full flexibility with your schedule in a fully remote setting for your control of a working day, powered by Hubstaff for transparency and fairness.
- softgateHome Office·
- Software development spanning over the complete life cycle in the area of device controlling.
- Creating software concepts and designs in collaboration with…
- 3PillarHome Office·
- Facilitate effective communication with client project stakeholders regarding project status and recommendations.
- Proficiency in the English language.
Job Post Details
Clinical Research Associate/ Senior CRA - Czech
Popis pracovní pozice
Druh nabídky práce
- Plný úvazek
Lokalita
Úplný popis pracovní pozice:
Work Schedule
Standard (Mon-Fri)Environmental Conditions
OfficeJob Description
Thermo Fisher Scientific: Join Us for a Global Impact
At Thermo Fisher Scientific, we offer meaningful careers that make a global difference. Join us in fulfilling our mission: empowering customers to enhance the world's health, cleanliness, and safety. We provide the resources needed to help our employees achieve their career aspirations and advance science through the research, development, and delivery of life-changing therapies. Our work encompasses laboratory, digital, and decentralized clinical trial services across over 100 countries. Your dedication to quality and accuracy will drive better health outcomes for people and communities worldwide.
Clinical Department Overview
Our clinical department is responsible for defining, developing, and delivering clinical programs. Our global Clinical Operations team, part of our PPD® clinical research services, offers comprehensive support for clinical trials, from study initiation to monitoring and study close-out, across both commercial and government contracts. Together, we assist clients in defining and developing clinical programs, reducing delays, and implementing high-quality, cost-effective clinical studies.
Discover Impactful Work
- Oversee and coordinate all aspects of the clinical monitoring and site management process.
- Conduct remote or on-site visits to assess protocol and regulatory compliance and manage necessary documentation.
- Navigate and manage procedures and guidelines from various sponsors and monitoring environments.
- As a site processes specialist, ensure trials adhere to approved protocols, ICH-GCP guidelines, regulations, and SOPs, safeguarding the rights, well-being, and data reliability of subjects.
- Ensure audit readiness.
- Develop collaborative relationships with investigational sites.
A Day in the Life
- Monitor and analyze investigator sites to identify process failures, taking corrective/preventive actions to ensure compliance and mitigate risks.
- Ensure data accuracy through SDR, SDV, and CRF review, applicable through on-site and remote monitoring activities.
- Record observations in reports and letters promptly, adhering to approved business writing standards.
- Expedite the communication of observed deficiencies and issues to clinical management and follow through to resolution.
- Provide trial status tracking and progress update reports to the Clinical Team Manager (CTM) as required.
- Ensure all essential documents are complete and compliant with ICH-GCP and applicable regulations, conducting on-site file reviews per project specifications.
- Respond to company, client, and regulatory requirements/audits/inspections as necessary.
Education and Experience
- Bachelor's degree in a life sciences-related field or equivalent experience, or a Registered Nursing certification, with relevant formal academic/vocational qualifications.
- Demonstrated understanding of ICH-GCP, EU, and FDA requirements.
- Experience with independent, on-site monitoring in a Pharmaceutical or Clinical Research Organization.
Knowledge, Skills, Abilities
- Proficiency in medical/therapeutic area knowledge and medical terminology.
- Well-developed critical thinking skills and strong attention to detail.
- Effective organizational and time management skills.
- Ability to work both independently and as part of a team.
- Proficiency in German (C1 level) and English.
Employee Wellbeing
Thermo Fisher Scientific values the health and well-being of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive.
We offer a competitive salary and benefits package, along with a flexible working culture where work-life balance is genuinely valued.