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Clinical affairs manager Jobs in Eppstein

Zuletzt aktualisiert: vor 7 Stunden
Sr. Clinical Research Associate

Sr. Clinical Research Associate

AvaniaHesse, DE
Vollzeit
Avania is hiring Senior Clinical Research Associates (Sr CRAs) .Avania’s ClinOps Team establishes, maintains and supports clinical trials. as a key member of the team, our Sr CRA pe...Mehr anzeigenZuletzt aktualisiert: vor 9 Tagen
  • Gesponsert
Manager

Manager

ABO EnergyWiesbaden, Germany
Vollzeit
Arbeite mit uns an einer zukunftsfähigen Energieversorgung!.Wir machen Erneuerbare aus Überzeugung : ABO Energy plant und errichtet weltweit Wind- und Solarparks sowie Batterie- und Wasserstoffproje...Mehr anzeigenZuletzt aktualisiert: vor 9 Tagen
Senior Operations Manager Public Hospitality (m / w / d)

Senior Operations Manager Public Hospitality (m / w / d)

Compass Group DeutschlandEschborn
Senior Operations Manager Public Hospitality (m / w / d).Wir sind Teil des weltgrößten Catering-Unternehmens mit Sitz in Eschborn und verantworten in unserem Geschäftsbereich die Segmente Öffentliche G...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
(Senior) Clinical Project Manager (f / m / d)

(Senior) Clinical Project Manager (f / m / d)

CureVacWiesbaden, DE
CureVac SE is a global biopharmaceutical company researching and developing novel drugs based on the natural molecule Messenger RNA (mRNA). Our focus is on prophylactic vaccines, innovative cancer i...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
(Senior) Manager, Medical Science Liaison, Therapy Development, Transcatheter Mitral and Tricuspid Therapies (Germany)

(Senior) Manager, Medical Science Liaison, Therapy Development, Transcatheter Mitral and Tricuspid Therapies (Germany)

Edwards LifesciencesGermany, Hessen, Remote
Homeoffice
Vollzeit
Innovation starts from the heart.At Edwards, we put patients first.We invest a significant proportion of our revenue towards research and development to drive and develop groundbreaking medical inn...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
General Affairs (m / f / d)

General Affairs (m / f / d)

MOBIS Parts Europe N.V.Eschborn, Deutschland
To strengthen our European headquarter in Frankfurt am Main, we are currently looking for a.European branch of Hyundai MOBIS, a worldwide leading supplier of genuine parts and accessories in the fi...Mehr anzeigenZuletzt aktualisiert: vor 3 Tagen
(Junior) Regulatory Affairs Manager (m / w / d) in Vollzeit oder Teilzeit (mind. 30 Stunden)

(Junior) Regulatory Affairs Manager (m / w / d) in Vollzeit oder Teilzeit (mind. 30 Stunden)

Dr. Neuberger HoldingWiesbaden, Hessen, DE
Du stellst die Einhaltung aller rechtlichen Erfordernisse in Bezug auf Inhaltsstoffe und Labelling inklusive Claims der kosmetischen Produkte auf dem europäischen Markt sicher.Du überwachst die Ein...Mehr anzeigenZuletzt aktualisiert: vor 3 Tagen
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AML Director (m / w / d)

AML Director (m / w / d)

Selby JenningsEschborn, Germany
Join a leading global consultancy firm dedicated to providing expert advisory services to clients across various industries. Our firm is committed to maintaining the highest standards of integrity a...Mehr anzeigenZuletzt aktualisiert: vor 9 Tagen
  • Gesponsert
Manager

Manager

Deutsche BankEschborn, Germany
Ebenso unterstützen Sie unsere internen Kolleg •innen aus den Bereichen Netzwerk und Telefonie bei der erfolgreichen Umsetzung von Projekten. Planung und Durchführung regelmäßiger Account Review Meet...Mehr anzeigenZuletzt aktualisiert: vor 9 Tagen
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Associate Director Medical Affairs all genders Allergan Aesthetics

Associate Director Medical Affairs all genders Allergan Aesthetics

AbbVieWiesbaden, Germany
Provides leadership to the Allergan Aesthetics Medical Affairs team including management coaching training and professional development support. Develops and implements the Allergan Aesthetics medic...Mehr anzeigenZuletzt aktualisiert: vor 16 Tagen
Experte Klinische Studien / Clinical Research Manager (Mensch)

Experte Klinische Studien / Clinical Research Manager (Mensch)

Lamm HR GmbHTaunus, HE, DE
Für unseren Kunden, die Heilerde-Gesellschaft Luvos Just GmbH & Co.KG, suchen wir Dich als Experten für Klinische Studien (m / w / d), der mit Leidenschaft und Fachwissen zur Weiterentwicklung natu...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
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Regulatory Affairs Manager (m / f / d) - In 3 Minuten erfolgreich bewerben

Regulatory Affairs Manager (m / f / d) - In 3 Minuten erfolgreich bewerben

palleos healthcare GmbHWiesbaden, Deutschland
REGULATORY AFFAIRS MANAGER (M / F / D) palleos healthcare is an international full-service CRO focused on Central and Eastern Europe. We offer clients in the pharmaceutical industry and biotech companie...Mehr anzeigenZuletzt aktualisiert: vor 7 Stunden
Product Manager (m / f / x) - Hemophilia

Product Manager (m / f / x) - Hemophilia

CSLEMEA, DE, Hattersheim, CSL Behring
Vollzeit
To strengthen our Business Unit Hemophilia & HAE, we are currently recruiting for a .Product Manager (m / f / x) - Hemophilia. Fulltime / permanent / Location : Hattersheim).We are looking to enhance our...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
Clinical Support Specialist - Middle East

Clinical Support Specialist - Middle East

Waters CorporationEschborn, HE, DE
Are you looking for an impactful role for a fast-growing company that helps advance science and human well-being?.Would you like the freedom of being field based where no day is the same and you ge...Mehr anzeigenZuletzt aktualisiert: vor 3 Tagen
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Regulatory Strategy Specialist (f / m / d)

Regulatory Strategy Specialist (f / m / d)

Deutsche Börse GroupEschborn, Germany
Join our international team that drives positive change, united by a spirit of openness and curiosity.We empower you to have an impact and to grow – personally and professionally.With us, you work ...Mehr anzeigenZuletzt aktualisiert: vor 8 Tagen
Manager Regulatory Affairs – Regulatory Reporting

Manager Regulatory Affairs – Regulatory Reporting

Aareal Bank AGWiesbaden, DE
Für diese anspruchsvolle Position suchen wir eine engagierte Persönlichkeit, die einen hohen Anspruch an Datenqualität und Ergebnisorientierung legt. Darauf können Sie sich freuen : .Mit Ihrer Experti...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
Clinical Psychologist

Clinical Psychologist

Cape Fox Federal Contracting GroupWiesbaden, Germany Wiesbaden, HE, DE
Vollzeit
Cape Fox Facilities Services (CFFS) is seeking experienced Behavioral Health professionals to provide advanced support services to the US Army in developing and implementing a tailored Health & Wel...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
Life Science Internship – Regulatory Affairs (m / f / d)

Life Science Internship – Regulatory Affairs (m / f / d)

Procter & GambleSchwalbach Am Taunus
Vollzeit
Are you curious to learn more how working in the Healthcare category of a big FMCG company looks like? Join our team near Frankfurt am Main and find out more!. During your internship we offer you th...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
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Sr. Clinical Research Associate

Sr. Clinical Research Associate

AvaniaHesse, DE
Vor 9 Tagen
Anstellungsart
  • Vollzeit
Stellenbeschreibung

Avania is hiring Senior Clinical Research Associates (Sr CRAs)

Avania’s ClinOps Team establishes, maintains and supports clinical trials; as a key member of the team, our Sr CRA performs clinical trial oversight for the trials, verifying that the rights and well-being of human subjects are protected, and that reported trial data are accurate, complete, and verifiable (from source documents). Partnering closely with our Trial sites, Avania's Sr CRA ensures that the conduct of the trial follows approved protocols / amendment(s), with ISO14155 or ICH-GCP, and with applicable regulatory requirements.

Our Senior CRA role includes the following key activities -

  • Interact with and guide study investigators and study coordinators in conducting clinical trials in accordance with study protocols. Member of a site Start-up Team for assigned projects.
  • Monitor site’s completion of action items between visits and help prepare for audits and inspections; conduct and write accurate visit reports in accordance with SOPs and GCP (SQV, SIV, IMV, COV)
  • Ensure data entered on the CRFs is timely, accurate and verified. Collaborate with analytical services to obtain clean database, resolve queries and conduct or participate in data reviews (both internally and with sponsor), identifying and communicating trends or erroneous data.
  • Participate in internal TMF reviews, as needed.
  • Develop and maintain trackers, such as visit reports trackers, site trackers, recruitment and enrollment trackers.
  • Review and write informed consent forms. Review of protocols, investigator brochures on compliance with applicable regulations and CRFs in development. Prepare clinical trial agreements and present to site and study sponsor.
  • Review regulatory compliance for study documents and protocols.
  • May act as a Clinical Lead, overseeing clinical trial activities at investigational sites (will require travel to investigational sites).

Candidates who offer a combination of the skills, knowledge and experience listed below are encouraged to apply. With our continued growth we are hiring talent to join us on our journey and grow with us.

Sr CRAs require skills in planning and preparation; sourcing and collecting information; prioritizing tasks and actions; and displaying a proactive attitude to assist in project planning and study execution.

We seek -

  • B.A. / B.S. or equivalent experience in a (para)medical, scientific or health related discipline or related work experience.
  • Minimum 3-7 years of relevant CRA work experience, with extensive cardiology Class III device monitoring experience.
  • Tracker and Start-up experience (with good spreadsheet or similar skills)
  • Ability to understand basic and complex medical details.
  • GCP-ICH-E6, FDA regulations and ISO 14155, 13485 and 9001 knowledge where applicable; knowledge of / ability to learn regulations and guidelines on medical devices and clinical trials.
  • Ability to travel up to 75% domestically and internationally.
  • Experience as a Clinical Lead helpful
  • Strong communicator with excellent presentation skills; able to build rapport with site personnel

    • We offer -

  • The opportunity to work in an innovative, fast-growing and rewarding industry
  • A dynamic and enthusiastic global team that fosters collaboration and the opportunity to work with experts across many specialties
  • Exchange of knowledge and ideas to help employees grow and advance their careers, backed with training and other development opportunities
  • Competitive compensation and benefits package (details shared during the interview process)
  • Some roles offer the opportunities for travel
  • Ask us about our hybrid and fully remote work opportunities

    • We look forward to receiving your application!

    When you need to advance your career, it takes Avania!

    LI-DNI