Aktuelle Jobs im Zusammenhang mit Clinical Research Associate - Frankfurt am Main, Hessen - Pharmiweb
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Clinical Research Associate
vor 4 Wochen
Frankfurt am Main, Hessen, Deutschland Pharmiweb VollzeitUnlock Your Potential as a Clinical Research AssociateAre you passionate about advancing medical treatments and improving patient outcomes? Do you have a strong foundation in life sciences and a desire to work in a dynamic, fast-paced environment? If so, we invite you to explore the exciting opportunity of a Clinical Research Associate role at Pharmiweb.As a...
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Clinical Research Associate
vor 4 Wochen
Frankfurt am Main, Hessen, Deutschland Pharmiweb VollzeitUnlock Your Potential as a Clinical Research AssociateAre you passionate about advancing medical treatments and improving patient outcomes? Do you have a strong foundation in life sciences and a desire to work in a dynamic, fast-paced environment? If so, we invite you to explore the exciting opportunity of a Clinical Research Associate role at Pharmiweb.As a...
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Clinical Research Associate
vor 1 Monat
Frankfurt am Main, Hessen, Deutschland IQVIA VollzeitUnlock Your Potential as a Clinical Research Associate at IQVIAAre you passionate about advancing medical research and making a meaningful impact in the healthcare industry? Do you possess excellent communication skills, attention to detail, and a strong understanding of clinical research regulations? If so, we invite you to explore this exciting opportunity...
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Clinical Research Associate
vor 1 Monat
Frankfurt am Main, Hessen, Deutschland IQVIA VollzeitUnlock Your Potential as a Clinical Research Associate at IQVIAAre you passionate about advancing medical research and making a meaningful impact in the healthcare industry? Do you possess excellent communication skills, attention to detail, and a strong understanding of clinical research regulations? If so, we invite you to explore this exciting opportunity...
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Clinical Research Associate
vor 1 Monat
Frankfurt am Main, Hessen, Deutschland IQVIA VollzeitUnlock Your Potential as a Clinical Research Associate at IQVIAAre you passionate about advancing medical research and making a meaningful impact in the healthcare industry? Do you possess excellent communication skills, attention to detail, and a strong understanding of clinical research regulations? If so, we invite you to explore this exciting opportunity...
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Clinical Research Associate
vor 4 Wochen
Frankfurt am Main, Hessen, Deutschland IQVIA VollzeitUnlock Your Potential as a Clinical Research Associate at IQVIAAre you passionate about advancing medical research and making a meaningful impact in the healthcare industry? Do you possess excellent communication skills, attention to detail, and a strong understanding of clinical research regulations? If so, we invite you to explore this exciting opportunity...
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Clinical Research Associate
vor 4 Wochen
Frankfurt am Main, Hessen, Deutschland IQVIA VollzeitUnlock Your Potential as a Clinical Research Associate at IQVIAAre you passionate about advancing medical research and making a meaningful impact in the healthcare industry? Do you possess excellent communication skills, attention to detail, and a strong understanding of clinical research regulations? If so, we invite you to explore this exciting opportunity...
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Clinical Research Associate
vor 4 Wochen
Frankfurt am Main, Hessen, Deutschland Pharmiweb VollzeitJob Title: Clinical Research AssociateWe are seeking a highly motivated and detail-oriented Clinical Research Associate to join our team at IQVIA. As a Clinical Research Associate, you will play a critical role in the success of our clinical trials by ensuring the quality and integrity of site practices.Responsibilities:Perform site selection, initiation,...
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Clinical Research Associate
vor 4 Wochen
Frankfurt am Main, Hessen, Deutschland Pharmiweb VollzeitJob Title: Clinical Research AssociateWe are seeking a highly motivated and detail-oriented Clinical Research Associate to join our team at IQVIA. As a Clinical Research Associate, you will play a critical role in the success of our clinical trials by ensuring the quality and integrity of site practices.Responsibilities:Perform site selection, initiation,...
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Clinical Research Associate
vor 2 Wochen
Frankfurt am Main, Hessen, Deutschland Pharmiweb VollzeitJob Title: Clinical Research AssociateWe are seeking a highly motivated and detail-oriented Clinical Research Associate to join our team at IQVIA. As a Clinical Research Associate, you will play a critical role in the success of our clinical trials by ensuring the quality and integrity of site practices.Responsibilities:Perform site selection, initiation,...
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Clinical Research Associate
vor 2 Wochen
Frankfurt am Main, Hessen, Deutschland Pharmiweb VollzeitJob Title: Clinical Research AssociateWe are seeking a highly motivated and detail-oriented Clinical Research Associate to join our team at IQVIA. As a Clinical Research Associate, you will play a critical role in the success of our clinical trials by ensuring the quality and integrity of site practices.Responsibilities:Perform site selection, initiation,...
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Clinical Research Associate
vor 4 Wochen
Frankfurt am Main, Hessen, Deutschland Pharmiweb VollzeitJob Title: Clinical Research Associate ContractorWe are seeking a highly skilled Clinical Research Associate Contractor to join our team. As a Clinical Research Associate, you will play a critical role in the success of our clinical trials.Key Responsibilities:Schedule, plan, and conduct site visits to ensure compliance with regulatory requirements and study...
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Clinical Research Associate
vor 4 Wochen
Frankfurt am Main, Hessen, Deutschland Pharmiweb VollzeitJob Title: Clinical Research Associate ContractorWe are seeking a highly skilled Clinical Research Associate Contractor to join our team. As a Clinical Research Associate, you will play a critical role in the success of our clinical trials.Key Responsibilities:Schedule, plan, and conduct site visits to ensure compliance with regulatory requirements and study...
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Clinical Research Associate
vor 2 Wochen
Frankfurt am Main, Hessen, Deutschland IQVIA VollzeitUnlock Your Potential as a Clinical Research Associate at IQVIAAre you passionate about advancing medical knowledge and improving patient outcomes? Do you have a strong foundation in life sciences and a desire to work in a dynamic, global environment? As a Clinical Research Associate at IQVIA, you'll have the opportunity to work on cutting-edge projects,...
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Clinical Research Associate
vor 2 Wochen
Frankfurt am Main, Hessen, Deutschland IQVIA VollzeitUnlock Your Potential as a Clinical Research Associate at IQVIAAre you passionate about advancing medical knowledge and improving patient outcomes? Do you have a strong foundation in life sciences and a desire to work in a dynamic, global environment? As a Clinical Research Associate at IQVIA, you'll have the opportunity to work on cutting-edge projects,...
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Clinical Research Associate
vor 1 Monat
Frankfurt am Main, Hessen, Deutschland IQVIA VollzeitJob Title: Experienced Clinical Research AssociateIQVIA is seeking an experienced Clinical Research Associate to join our Clinical Site Management department in Germany. As a key member of our team, you will be responsible for conducting monitoring visits on complex clinical trials for various pharmaceutical companies, ensuring adherence to good clinical...
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Clinical Research Associate
vor 1 Monat
Frankfurt am Main, Hessen, Deutschland IQVIA VollzeitJob Title: Experienced Clinical Research AssociateIQVIA is seeking an experienced Clinical Research Associate to join our Clinical Site Management department in Germany. As a key member of our team, you will be responsible for conducting monitoring visits on complex clinical trials for various pharmaceutical companies, ensuring adherence to good clinical...
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Clinical Research Associate
vor 4 Wochen
Frankfurt am Main, Hessen, Deutschland IQVIA VollzeitJob Title: Experienced Clinical Research AssociateIQVIA is seeking an experienced Clinical Research Associate to join our Clinical Site Management department in Germany. As a key member of our team, you will be responsible for conducting monitoring visits on complex clinical trials for various pharmaceutical companies, ensuring adherence to good clinical...
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Clinical Research Associate
vor 4 Wochen
Frankfurt am Main, Hessen, Deutschland IQVIA VollzeitJob Title: Experienced Clinical Research AssociateIQVIA is seeking an experienced Clinical Research Associate to join our Clinical Site Management department in Germany. As a key member of our team, you will be responsible for conducting monitoring visits on complex clinical trials for various pharmaceutical companies, ensuring adherence to good clinical...
Clinical Research Associate
vor 1 Monat
We are seeking a highly skilled Clinical Research Associate to join our team in Germany. As a Clinical Research Associate, you will play a critical role in the success of our clinical trials by ensuring the smooth execution of study protocols, managing site relationships, and maintaining compliance with regulatory requirements.
Key Responsibilities:- Schedule, plan, and conduct site visits to ensure compliance with study protocols and regulatory requirements.
- Write and submit reports and investigator follow-up letters to ensure timely and accurate communication with sites.
- Manage the progress of assigned studies by tracking regulatory/IRB submissions and approvals, recruitment and enrollment, CRF completion and submission, and data query generation and resolution.
- Provide project updates to the project management team to ensure seamless communication and collaboration.
- Organize the delivery of investigational product, laboratory supplies, CRFs, and other study-specific materials to and from clinical sites.
- Perform investigational product inventory and ensure the return of unused investigational product to designated locations or verify destruction as required.
- Assist with preparing for and attending investigator meetings for assigned studies.
- Review study documents for compliance with protocol, ICH GCP guidelines, protocol deviations/violations, and waivers, and review study documents for subject safety events; escalate issues at site to project management.
- Collect and review essential study documents from sites for filing in eTMF.
- Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
- Evaluate the quality and integrity of study site practices related to the proper conduct of the study and ensure adherence to applicable regulations.
- Compliance: Follow international GCP guidelines/regulations and SOPs for executing clinical studies. Participate in the planning of quality assurance activities and coordinate the resolution of audit findings.
- Assist the Clinical Trial Manager with clinical operations activities by overseeing resource allocation, reviewing site performance, providing feedback to CRAs and CTAs, resolving issues, performing review and oversight of site visit reports.
- May review protocols, eCRFs, study manuals, and other study-related documents, as requested by the Clinical Trial Manager.
- May conduct on-site evaluation visits and on-site training of CRAs.
- Lead and participate in regular team meetings/teleconferences.
- Assist, as appropriate, with reporting site performance regarding timelines and deliverables during project team meetings and assist with providing and compiling feedback for analysis of overall study performance.
- May serve as a mentor to associates on the subject of job performance, trainings, and professional growth.
- Bachelor's degree in biomedical sciences or a related scientific discipline.
- Fluent English (oral and written) and applicable local business language.
- Minimum three years of monitoring experience, more experience preferred, with a combination of clinical research coordinator and/or other relevant clinical research experience.
- Sound knowledge of medical terminology and advanced proficiency in clinical monitoring process.
- Ability to travel up to 70%, depending on project requirements.
- Good knowledge and understanding of ICH GCP and worldwide applicable regulatory requirements.
- Excellent verbal, written communication, and presentation skills.
- Good leadership, planning, project management skills, verbal communication skills, and written communication skills.
- Knowledge and experience with MS Office suite (at a minimum Word, PowerPoint, and Excel).
If you have the experience required and want to join a dynamic and collaborative team, please apply directly to our website at https://www.pharmiweb.com or email us.
