20 beste Stellen als data science in home office – aktuell auf Personalsuche

CRA I/II - FSP
Thermo Fisher Scientific —Home Office
- Vollzeit
- Englisch
- Microsoft Office
- Präsentationserfahrung
Assistant CRA (m/f/d) (Open)
Thermo Fisher Scientific —Home Office
- Vollzeit
- Homeoffice
- Kundenberatung
- Forschungserfahrung
- Microsoft Office
- Aufstiegsmöglichkeiten
Data Analyst (m/w/d)
420Cloud GmbH —Home Office
- 34.000 € – 41.000 € pro Jahr
- Teilzeit
- Homeoffice
- Datenanalyse
- Datenbanken
- SQL
- Homeoffice-Möglichkeit
- Weiterbildungsprogramme
Direkt bewerben
1 Tag
Data Scientist Industry (F/M/D)
Xplain Data GmbH —Home Office
- Vollzeit
- Homeoffice
- Machine Learning
- Künstliche Intelligenz
- Python
- Homeoffice-Möglichkeit
- Flexible Arbeitszeiten
Data Scientist (m/f/x)
FINN —Home Office
- 69.000 € – 80.000 € pro Jahr
- Vollzeit
- Homeoffice
- Doktorat
- Master
- SQL
Direkt bewerben
Working Student: Life Cycle Assessment & Carbon Accounting for Plastics Recycling
ECOTA GmbH —Home Office
- Ab 14 € pro Stunde
- Homeoffice
- Rechnungswesen
- Homeoffice-Möglichkeit
- Flexible Arbeitszeiten
Direkt bewerben
10 Std.
Studentischer Minijob (m/w/d) – KI-gestützte Automatisierungen
E-Commerce Annika Witeczek —Home Office
- 15 € pro Stunde
- Montag bis Freitag
- Homeoffice
- Informatik
- Hochschulreife
- JavaScript
- Homeoffice-Möglichkeit
- Flexible Arbeitszeiten
Direkt bewerben
3 Tage
Data Scientist & AI-Engineer
Smateso GmbH —Home Office
- 15 € – 18 € pro Stunde
- Hybrides Arbeiten
- Englisch
- Machine Learning
- Künstliche Intelligenz
- Weiterbildungsprogramme
- Flexible Arbeitszeiten
Data Product Manager - OpenData Europe
Veeva Systems —Home Office
- 75.000 € – 120.000 € pro Jahr
- Vollzeit
- Homeoffice
- Informatik
- SQL
- Bachelor
- Homeoffice-Möglichkeit
Software Engineer, Data Infrastructure & Acquisition
Speechify —Home Office
- Homeoffice
- Doktorat
- Informatik
- Master
Data Warehouse & BI Engineer (m/w/d)
Studiengemeinschaft Werner Kamprath Darmstadt GmbH —Home Office
- Vollzeit
- Homeoffice
- Azure
- Informatik
- DevOps
Field Applications Scientist (m/f/d) – NGS Bioinformatics
Thermo Fisher Scientific —Home Office
- Vollzeit
- Homeoffice
- Software-Fehlerbehebung
- Master
- Bachelor
Data Scientist & Solution Manager (Health) (F/M/D)
Xplain Data GmbH —Home Office
- Vollzeit
- Homeoffice
- Datenanalyse
- Künstliche Intelligenz
- Python
- Homeoffice-Möglichkeit
- Flexible Arbeitszeiten
AI & Data Engineer (m/w/d)
PeakSoft GmbH —Home Office
- Vollzeit
- Homeoffice
- Informatik
- Englisch
- Machine Learning
- Homeoffice-Möglichkeit
Direkt bewerben
7 Tage
Sr CRA I/II - FSP - Germany
Thermo Fisher Scientific —Home Office
- Vollzeit
- Homeoffice
- Englisch
- Microsoft Office
- Präsentationserfahrung
11 Tage
Praxissemester als Data Scientist – KI / AI (m/w/d)
XiLLeR GmbH —Home Office
- Per E-Mail
- Homeoffice
- Machine Learning
- Künstliche Intelligenz
- Praktikum
- Gleitzeit
- Homeoffice-Möglichkeit
Direkt bewerben
Backend Engineer
FAIRTIQ AG —Home Office
- Teilzeit
- Homeoffice
- Schreibfähigkeiten
- Systemdesign
- Englisch
- Flexible Arbeitszeiten
Product Designer (Platform)
Revolut —Home Office
- Vollzeit
- Homeoffice
- Informatik
- Master
- Bachelor
Clinical Research Associate I - Real World Late Phase
Syneos - Clinical and Corporate - Prod —Home Office
- Vollzeit
- Homeoffice
- Bachelor
- Wirtschaft
Data Scientist - KI und ML - FinTech (w/m/d)
Europace Ratenkredit GmbH —Home Office
- Vollzeit
- Homeoffice
- Master
- Machine Learning
- Agile
- Flexible Arbeitszeiten
Direkt bewerben
1 Tag

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CRA I/II - FSP

Thermo Fisher Scientific -
Home Office

Jetzt bewerben

Details zur Stelle

Vollzeit

Qualifikationen

Prozessverbesserung
Englisch
Microsoft Office
Präsentationserfahrung
Bachelor
PC-Kenntnisse
Medizinische Fachbegriffe
Zeitmanagement

Vollständige Stellenbeschreibung

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Join Us as a Clinical Research Associate (Level II) – Make an Impact at the Forefront of Innovation
We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years. This opportunity is an exciting prospect for a big pharma company and for a new division focused on Oncology/Cell therapy.

As part of our global team, you’ll have the opportunity to perform and coordinate all aspects of the clinical monitoring and site management process. As a Clinical Research Associate (Level II), you'll conduct remote or on-site visits to assess protocol and regulatory compliance and manage required documentation. You will manage procedures and guidelines from different sponsors and/or monitoring environments (i.e., FSO, FSP, Government, etc.). Acting as a site processes specialist, you will ensure that the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations, and SOPs to guarantee subjects' rights, well-being, and data reliability. You will ensure audit readiness and develop collaborative relationships with investigational sites. Detailed tasks and responsibilities assigned to your role are outlined in the task matrix.

What You’ll Do:

Monitors investigator sites with a risk-based monitoring approach: applies root cause analysis (RCA), critical thinking and problem-solving skills to identify site processes failure and corrective/preventive actions to bring the site into compliance and decrease risks. Ensures data accuracy through SDR, SDV and CRF review as applicable through on-site and remote monitoring activities. Assess investigational product through physical inventory and records review. Documents observations in reports and letters in a timely manner using approved business writing standards. Escalates observed deficiencies and issues to clinical management expeditiously and follow all issues through to resolution. May need to maintain regular contact between monitoring visits with investigative sites to confirm that the protocol is being followed, that previously identified issues are being resolved and that the data is being recorded in a timely manner. Conducts monitoring tasks in accordance with the approved monitoring plan. Participates in the investigator payment process. Ensures a shared responsibility with other project team members on issues/findings resolution. Investigates and follows-up on findings as applicable.
Participates in investigator meetings as necessary. Identifies potential
investigators in collaboration with the client company to ensure the acceptability of qualified investigative sites. Initiates clinical trial sites according to the relevant procedures to ensure compliance with the protocol and regulatory and ICH GCP obligations, making recommendations where warranted. Performs trial close out and retrieval of trial materials.
Ensures that required essential documents are complete and in place, according to ICH-GCP and applicable regulations. Conducts on-site file reviews as per project specifications.
Provides trial status tracking and progress update reports to the Clinical Team Manager (CTM) as required. Ensures study systems are updated per agreed study conventions (e.g. Clinical Trial Management System).
Facilitates effective communication between investigative sites, the client company and the PPD project team through written, oral and/or electronic contacts.
Responds to company, client and applicable regulatory requirements/audits/inspections.
Maintains & completes administrative tasks such as expense reports and timesheets in a timely manner.
Contributes to the project team by assisting in preparation of project publications/tools, and sharing ideas/suggestions with team members.
Contributes to other project work and initiatives for process improvement, as required.

Education and Experience Requirements:

Bachelor's degree in a life science related fieldor a Registered Nursing certification or equivalent and relevant formal academic / vocational qualification.

Total experience: at least 2 years as a CRA
Oncology/Cell therapy experience: at least 2 years of on-site, hands-on experience
Location: Germany

Valid driver's license where applicable.

Knowledge, Skills and Abilities:

Proven clinical monitoring skills
Demonstrated understanding of medical/therapeutic area knowledge and medical terminology
Demonstrated ability to attain and maintain a working knowledge of ICH GCPs, applicable regulations and procedural documents
Well-developed critical thinking skills, including but not limited to: critical mindset, in-depthinvestigation for appropriate root cause analysis and problem solving
Ability to manage Risk Based Monitoring concepts and processes
Good oral and written communication skills, with the ability to communicate effectively with medical personnel
Ability to maintain customer focus through the utilization of good listening skills, attention to detail and the ability to perceive customers’ underlying issues
Good organizational and time management skills
Effective interpersonal skills
Attention to detail
Ability to remain flexibile and adaptable in a wide range of scenarios
Ability to work in a team or independently as required
Good computer skills: solid knowledge of Microsoft Office and the ability to learn appropriate software
Good English language and grammar skills
Good presentation skills

Working Conditions and Environment:

Work is performed in an office/ laboratory/clinical/and/or home office environment with exposure to electrical office equipment.
Frequent drives to site locations. Frequent travel, generally 60-80% but more for some individuals. May also include extended overnight stays.
Exposure to biological fluids with potential exposure to infectious organisms.
Personal protective equipment required such as protective eyewear, garments and gloves.
Exposure to fluctuating and/or extreme temperatures on rare occasions

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Erweiterte Suche

data science Jobs in home office

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Data Analyst (m/w/d)

Data Scientist Industry (F/M/D)

Data Scientist (m/f/x)

Working Student: Life Cycle Assessment & Carbon Accounting for Plastics Recycling

Studentischer Minijob (m/w/d) – KI-gestützte Automatisierungen

Data Scientist & AI-Engineer

Data Product Manager - OpenData Europe

Software Engineer, Data Infrastructure & Acquisition

Data Warehouse & BI Engineer (m/w/d)

Field Applications Scientist (m/f/d) – NGS Bioinformatics

Data Scientist & Solution Manager (Health) (F/M/D)

AI & Data Engineer (m/w/d)

Sr CRA I/II - FSP - Germany

Praxissemester als Data Scientist – KI / AI (m/w/d)

Backend Engineer

Product Designer (Platform)

Clinical Research Associate I - Real World Late Phase

Data Scientist - KI und ML - FinTech (w/m/d)

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