20 beste Stellen als data science in norderstedt – aktuell auf Personalsuche

Clinical Research Associate I (CRA I) / Klinischer Monitor – Full-Time or Part-Time Available (m/w/d)
Thermo Fisher Scientific —Hamburg
- Vollzeit
- Präsentationserfahrung
- Bachelor
- Mit Reiseanteil
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- Flexible Arbeitszeiten
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tesa —Hamburg
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- Teilzeit
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PhD Student for development of strategies for GHz speckle experiments (f/m/d) - 29,25 hours/week
European X-Ray Free-Electron Laser Facility GmbH —Schenefeld
- 4.901,11 € – 5.279,32 € pro Monat
- Teilzeit
- Master
- Homeoffice-Möglichkeit
- Flexible Arbeitszeiten
PhD Student (f/m/d) for two-color imaging studies - 29,25 hours/week
European X-Ray Free-Electron Laser Facility GmbH —Schenefeld
- 4.901,11 € – 5.279,32 € pro Monat
- Teilzeit
- Master
- Homeoffice-Möglichkeit
- Flexible Arbeitszeiten
9 Tage
Student Assistant for IT Support (f/m/d)
European X-Ray Free-Electron Laser Facility GmbH —Schenefeld
- 2.975,32 € – 3.164,20 € pro Monat
- Teilzeit
- Master
- Bachelor
- Homeoffice-Möglichkeit
- Flexible Arbeitszeiten
Working Student (m/f/d) – Laboratory Preparation & Testing of Innovative High-Performance Materials
tesa —Hamburg
- Teilzeit
Research Associate for the Project “Human-AI Teaming Therapeutic Companion for Torture Survivors with PTSD”
Universität Hamburg —Hamburg
- Teilzeit
- Master
- Flexible Arbeitszeiten
12 Tage
Post doctoral researcher for hard X-ray attosecond science (f/m/d)
European X-Ray Free-Electron Laser Facility GmbH —Schenefeld
- 4.901,70 € – 7.025,87 € pro Monat
- Vollzeit
- Doktorat
- Homeoffice-Möglichkeit
- Flexible Arbeitszeiten
Data Scientist – Optimization (m/w/d)
EUROGATE GmbH & Co. KGaA, KG —Hamburg
- Doktorat
- Informatik
- AWS
- Employee Assistance Program
Working Student Energy Data Analyst (m/w/d)
1Komma5° GmbH —Hamburg
- Teilzeit
- Informatik
Direkt bewerben
Working Student – Laboratory Preparation & Testing of Innovative High-Performance Materials (m/f/x)
tesa —Hamburg
- 1.519 € pro Monat
- Teilzeit
- Reisekostenerstattung
- Flexible Arbeitszeiten
Werkstudent Scientific Affairs & KI-Innovation (m/w/d)
Waldemar Link Gmbh & Co. KG —Norderstedt
- 17 € – 19 € pro Stunde
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- Datenanalyse
- Englisch
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Working Student (m/f/d) Data Analytics & Process Automation
Nordex SE —Hamburg
- 17 € pro Stunde
- Vollzeit
- Informatik
- Flexible Arbeitszeiten
11 Tage
Research Associate for the Project “Don’t fear the reaper – the role of apoptosis in controlling phytoplankton populations in a changing world”
Universität Hamburg —Hamburg
- Teilzeit
- Doktorat
- Flexible Arbeitszeiten
3 Tage
Research Associate for the “International Max Planck Research School on Earth System Modelling” (IMPRS-ESM)
Universität Hamburg —Hamburg
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Research Associate for the Project “Observational studies of compact hot stars using large scale sky surveys”
Universität Hamburg —Hamburg
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2 Tage
Data Engineer Wind Energy (m/f/d)
Nordex SE —Hamburg
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Data Scientist
DEVnet Holding —Hamburg
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- Mit Reiseanteil
Laser-Plasma Acceleration Scientist for Active Stabilization and Machine Learning for PETRA IV
Deutsches Elektronen-Synchrotron DESY —Hamburg
- Teilzeit
- Doktorat
- Homeoffice-Möglichkeit
- Flexible Arbeitszeiten
5 Tage

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data science jobs near norderstedt

Clinical Research Associate I (CRA I) / Klinischer Monitor – Full-Time or Part-Time Available (m/w/d)

Thermo Fisher Scientific -
Hamburg

Jetzt bewerben

Details zur Stelle

Vollzeit

Qualifikationen

Prozessverbesserung
Präsentationserfahrung
Bachelor
Zeitmanagement

Vollständige Stellenbeschreibung

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.

Our clinical department defines, develops and delivers clinical programmes. Our global Clinical Operations colleagues within our PPD® clinical research services provide end-to-end support for clinical trials from study start up to monitoring through to study close out, across commercial and government contracts. Together, we help clients define and develop clinical programs, minimize delays, and implement high-quality, cost-efficient clinical studies.

The role can be home-based, office-based in Munich or Karlsruhe, or hybrid, and is offered as a permanent full time (1 FTE) or part-time position (0.8 FTE / 80%).

The CRA:

Performs and coordinates all aspects of the clinical monitoring and site management process.
Conducts remote or on-site visits to assess protocol and regulatory compliance and manages required documentation..
Acts as a site processes specialist, ensuring 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.
Ensures audit readiness.
Develops collaborative relationships with investigational sites.
Detailed tasks and responsibilities assigned to role are outlined in the task matrix.
Travel up to 50-75%

A day in the Life:

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.
Brings up 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
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, CTMS).
Performs QC check of reports generated from CTMS system where required.
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. Ensures 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.
Gives to the project team by assisting in preparation of project publications/tools and sharing ideas/suggestions with team members. Performs additional study tasks as assigned by CTM (e.g. trip report review, newsletter creation, lead CRA team calls etc).
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.
Gives to other project work and initiatives for process improvement, as required.

Education and Experience

Bachelor's degree in a life sciences related field or equivalent and relevant formal academic / vocational qualification.
Previous experience in a clinical environment with exposure to clinical research, healthcare or clinical trials that provides the knowledge and skills required to perform the role
Valid driver's license
Full Right to work in Germany
Fluency in English and German language to at least C1 level (note that the interview will be held in German).

Knowledge, Skills, Abilities

Effective clinical monitoring skills
Demonstrated understanding of medical/therapeutic area knowledge and medical terminology
Excellent understanding and demonstrated application of ICH GCPs, applicable regulations and procedural documents
Well-developed critical thinking skills, including but not limited to: critical attitude, in-depth investigation for appropriate root cause analysis and decision-making
Ability to handles Risk Based Monitoring concepts and processes
Effective 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
Effective social skills
Strong attention to detail
Effective organizational and time management skills
Ability to remain flexible and adaptable in a wide range of scenarios
Ability to work in a team or independently as required
Good computer skills: proficient knowledge of Microsoft Office and the ability to learn appropriate software
Good presentation skills

Severely disabled applicants with the same aptitude will be given preferential treatment. / Schwerbehinderte Bewerber werden bei gleicher Eignung bevorzugt behandelt.

Jetzt bewerben

Erweiterte Suche

data science Jobs in norderstedt

Clinical Research Associate I (CRA I) / Klinischer Monitor – Full-Time or Part-Time Available (m/w/d)

Research Scientist (all genders) Discovery Data integration

Working Student – Data Administration, Data Quality & Analysis (Strategic Core Project) (m/f/x)

PhD Student for development of strategies for GHz speckle experiments (f/m/d) - 29,25 hours/week

PhD Student (f/m/d) for two-color imaging studies - 29,25 hours/week

Student Assistant for IT Support (f/m/d)

Working Student (m/f/d) – Laboratory Preparation & Testing of Innovative High-Performance Materials

Research Associate for the Project “Human-AI Teaming Therapeutic Companion for Torture Survivors with PTSD”

Post doctoral researcher for hard X-ray attosecond science (f/m/d)

Data Scientist – Optimization (m/w/d)

Working Student Energy Data Analyst (m/w/d)

Working Student – Laboratory Preparation & Testing of Innovative High-Performance Materials (m/f/x)

Werkstudent Scientific Affairs & KI-Innovation (m/w/d)

Working Student (m/f/d) Data Analytics & Process Automation

Research Associate for the Project “Don’t fear the reaper – the role of apoptosis in controlling phytoplankton populations in a changing world”

Research Associate for the “International Max Planck Research School on Earth System Modelling” (IMPRS-ESM)

Research Associate for the Project “Observational studies of compact hot stars using large scale sky surveys”

Data Engineer Wind Energy (m/f/d)

Data Scientist

Laser-Plasma Acceleration Scientist for Active Stabilization and Machine Learning for PETRA IV

Ich möchte aktuelle Job-E-Mails für Stellen als data science in norderstedt erhalten

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