20 beste Stellen als laboratory in frankfurt (main) niederrad – aktuell auf Personalsuche

Clinical Research Associate I (CRA I) / Klinischer Monitor – Full-Time or Part-Time Available (m/w/d)
Thermo Fisher Scientific —Frankfurt am Main
- Vollzeit
- Präsentationserfahrung
- Bachelor
- Mit Reiseanteil
Embryologist (m/f/d)
Fertility Center Darmstadt MVZ —Darmstadt
- Wochenendarbeit möglich
- Führungserfahrung
Ph.D. Position in Microbiome, Cancer, and Circadian Rhythm Research
Chemotherapeutisches Forschungsinstitut Georg-Speyer-Haus —Frankfurt am Main
- Doktorat
- Master
Technical Application Scientist II, Chemistry, German and English speaker, Fixed Term (18 months)
Thermo Fisher Scientific —Darmstadt
- Vollzeit
- Doktorat
- Master
Laboratory Technician Innovation (m/w/d)
Heraeus Holding GmbH —Wehrheim
- Online-Bewerbung
- Employee Assistance Program
Senior Analytical Scientist (Full-/Part-time) (all genders)
Merck KGaA —Darmstadt
- Teilzeit
- Master
11_Frankfurt_SBiK-F_ENG
Senckenberg Gesellschaft für Naturforschung —Frankfurt am Main
- Teilzeit
- Doktorat
- Kommunikationsfähigkeit
- Flexible Arbeitszeiten
10 Tage
#11-26017 PostDoc Biomarker (m/f/d)
Senckenberg Gesellschaft für Naturforschung (SGN) —Frankfurt am Main
- Teilzeit
- Doktorat
- Kommunikationsfähigkeit
- Flexible Arbeitszeiten
10 Tage
Working student – Research & Development (m/f/d)
Procter & Gamble —Kronberg
- 21,75 € pro Stunde
- Teilzeit
- Master
- Elektrotechnik
- Führungserfahrung
Translational Medicine Operations Global Biospecimen Project & Team Leader - all genders
Sanofi —Frankfurt am Main
- 83.856 € – 125.784 € pro Jahr
- Master
- Präsentationserfahrung
- Bachelor
Food Inspector (Part-time/Freelancer)
QIMA —Frankfurt am Main
- Teilzeit
Direkt bewerben
4 Tage
Digital Scientist & Programme Coordinator
BMI Deutschland GmbH —Heusenstamm
- Vollzeit
- Master
- Bachelor
- Mit Reiseanteil
- Flexible Arbeitszeiten
14 Tage
Employee (m/f/d) - Sample Laboratory for Beverages and Food
Döhler GmbH —Darmstadt
- Empfehlungsprogramm
Customer Service / Installation Coordinator (m/f/d) DACH
Thermo Fisher Scientific —Dreieich
- Vollzeit
- Mit Reiseanteil
- Kommunikationsfähigkeit
Clinical Quality Manager (m/f/d)
Merz Aesthetics GmbH —Frankfurt am Main
- Vollzeit
- Master
- Gleitzeit
Direkt bewerben
Doctoral Candidate (f/m/d) in the Department of Music
Max-Planck-Institut für empirische Ästhetik —Frankfurt am Main
- Teilzeit
- Doktorat
- Master
- Psychologie
Direkt bewerben
1 Tag
Specialist, Technology Integration (m/w/d)
exocad gmbh —Darmstadt
- Vollzeit
- Flexible Arbeitszeiten
Project Manager Synthetics
BMI Deutschland GmbH —Heusenstamm
- Vollzeit
- Doktorat
- Mit Reiseanteil
- Führungserfahrung
- Kostenloser Parkplatz
- Flexible Arbeitszeiten
4 Tage
German-Speaking Technical Support Specialist II
Nova Biomedical —Frankfurt am Main
- Vollzeit
- Ohne Hochschulabschluss
- Kommunikationsfähigkeit
Direkt bewerben
Digital Workflow Specialist – BENELUX (f/m/d)
SprintRay —Weiterstadt
- Homeoffice
- Mit Reiseanteil
- Flexible Arbeitszeiten

Ich möchte aktuelle Job-E-Mails für Stellen als laboratory in frankfurt (main) niederrad erhalten

Wenn Sie sich bei Ihrem Konto anmelden, stimmen Sie den Nutzungsbedingungen, den Richtlinien zur Verwendung von Cookies sowie der Datenschutzerklärung von SimplyHired zu.

Weitere Job-Standorte erkunden

laboratory jobs near frankfurt (main) niederrad

Jobs als Researcher in Frankfurt Am Main

Jobs als Physician in Frankfurt Am Main

Jobs als Quality Manager in Frankfurt Am Main

Jobs als Clinical Research Associate in Frankfurt Am Main

Jobs als Engineer in Frankfurt Am Main

Jobs als Customer Service Coordinator in Wiesbaden

Jobs als Customer Service Coordinator in Berlin

Jobs als Customer Service Coordinator in München

Jobs als Researcher in Stuttgart

Jobs als User Experience Researcher in Berlin

Jobs als Researcher in München

Jobs als Quality Inspector M W D in Kupferzell

Jobs als Superintendent, Inspector Marine in Hamburg

Jobs als Inspector in Dortmund

Jobs als Senior Scientist in Heidelberg

Jobs als Senior Projektmanager in München

Jobs als Senior Scientist in München

Jobs als Senior Accountant in Hamburg

Jobs als Physician Assistant in Stuttgart

Jobs als Physician Assistant Studium Ausbildung in Nordrhein Westfalen

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

Thermo Fisher Scientific -
Frankfurt am Main

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

laboratory Jobs in frankfurt (main) niederrad

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

Embryologist (m/f/d)

Ph.D. Position in Microbiome, Cancer, and Circadian Rhythm Research

Technical Application Scientist II, Chemistry, German and English speaker, Fixed Term (18 months)

Laboratory Technician Innovation (m/w/d)

Senior Analytical Scientist (Full-/Part-time) (all genders)

11_Frankfurt_SBiK-F_ENG

#11-26017 PostDoc Biomarker (m/f/d)

Working student – Research & Development (m/f/d)

Translational Medicine Operations Global Biospecimen Project & Team Leader - all genders

Food Inspector (Part-time/Freelancer)

Digital Scientist & Programme Coordinator

Employee (m/f/d) - Sample Laboratory for Beverages and Food

Customer Service / Installation Coordinator (m/f/d) DACH

Clinical Quality Manager (m/f/d)

Doctoral Candidate (f/m/d) in the Department of Music

Specialist, Technology Integration (m/w/d)

Project Manager Synthetics

German-Speaking Technical Support Specialist II

Digital Workflow Specialist – BENELUX (f/m/d)

Ich möchte aktuelle Job-E-Mails für Stellen als laboratory in frankfurt (main) niederrad erhalten

Related Searches

Weitere Job-Standorte erkunden

The CRA:

A day in the Life:

Education and Experience

Knowledge, Skills, Abilities

Tools für Jobsuchende

Arbeitgebertools

Durchsuchen

Bleiben Sie in Kontakt