Clinical Safety Associate Stellenangebote

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39 Stellenangebote

Stellenangebote Clinical Safety Associate Jobs bei Neuvoo.com

Stellenangebot Clinical Safety Associate Job bei Oxford Global Resources

Job vor 3 Tagen gefunden Oxford Global Resources

Freelance CRA- Medical Devices (German/ English)

• Frankfurt Freiberuflich

MEHR

[...] would have 0. 7 to 1 FTE availability to give them support in managing sites in Germany, Switzerland and Austria. Remote opportunity + Up to 80 travel is possible. Job Description As a CRA you will be responsible for managing clinical activities at study sites conducting studies for Medical Devices. You will perform site management and monitoring activities and act as [...] study site and over all study metrics including but not limited to enrollment, deviations, adverse events, trial master file maintenance. Attends internal and external meetings as required. Provides all job- related progress reports and visit documentation as required. May support safety activities such as narrative writing, managing the CEC/ DSMB, etc. Prepares and coordinates submissions to regulatory authorities. May perform other activities as assigned. Requirements Higher education degree or equivalent education, training, and experience. +2 years experience as a Clinical Research Associate Experience in monitoring medical device studies. Fluency in English and German. Understanding of clinical research processes and regulations. Certifications such [...]
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Stellenangebote Clinical Safety Associate Jobs bei Jobleads

Job vor 7 Tagen gefunden Associate Director- (Senior) Patient Safety Physician (gn) : Oncology Baden- Württemberg, German. . . Führungs-/ Leitungspositionen

MEHR

Associate Director- (Senior) Patient Safety Physician (gn) : Oncology Baden- Württemberg, Germany, or relocation to Germany (relocation assistance available) . #clientvacancy #director [...] (Bio) Pharmaceutical Companies Your primary focus will revolve around orchestrating the global initiatives for Patient Safety and Pharmacovigilance (PSPV) and Risk Management (RM) pertaining to compounds at various stages of development. In this role, you will work closely with the clinical development department and will be involved in a very strategic and global function. TASKS RESPONSIBILITIES: Crafting proactive, patient- centric RM [...]

Job vom 22.07.2024

Associate Medical Director ( Hematology ) - (, , Remote)

Führungs-/ Leitungspositionen

MEHR

Associate Medical Director ( Hematology ) - (, , Remote) Sign up with scientific. today to see all content and to create a personalized stream of news, jobs and events, by defining keywords andfollowing your favorite content sources. Medical monitoring answering day to day medical and scientific questions, provide daily medical support to Parexel staff or site Safety monitoring Review and sign off adverse reports for accuracy and medical consistency, provide support for preparation of Periodic Safety Update Reports, review and sign off data listings for safety data, review adverse events and concomitant medications coding for accuracy and consistency. Provide medical expertise and training to Parexel personnel, sponsor, or site Provide medical support for the preparation of clinical protocols, final study report, statistical summary reports Provide medical input into pharmacovigilance workflows and projects, feasibility studies, Data Monitoring, Committees [...]
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Job vom 19.06.2024 Neurology Medical Director (Associate/ Senior) Führungs-/ Leitungspositionen

MEHR

Neurology Medical Director (Associate/ Senior) Apply At Job Full Name First Name Last Name Email Whats App Number Upload CV Please upload CV in [...] only. CV PDF Link User Profile Job Description: You can find fulfilling work that has a positive global impact at Thermo Fisher Scientific. Lets work as a team to achieve our goal of enabling our clients to enhance the planets safety, cleanliness, and health. We push science forward by conducting groundbreaking research, developing ground- breaking treatments, and supplying our teams with the tools necessary to help each member of the team realize their professional ambitions. Our work encompasses laboratory, digital, and decentralized clinical trial services, with clinical trials carried out in more than 100 countries and the continuous development of innovative frameworks for [...]
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Job vom 12.06.2024

Site Care Partner- FSP ( Germany) - (, , Remote)

MEHR

[...] contact for investigative sites and accountable for site start- up activities through activation, building, and retaining investigator site relationships. Providing support from site recommendation through the lifecycle of studies Site- level recruitment and operational success. Safeguarding the quality and patient safety at the investigator site. Contributing to country and site selection activities by proactively collaborating with key stakeholders and providing local intelligence to country outreach surveys, investigator strategies, and client pipeline opportunities under supervision. Experience required: Demonstrated experience in site management with prior experience as a Clinical Research Associate or Lead CRA. Demonstrated experience in startup activities through site activation. Demonstrated experience in conducting and close- out activities. Demonstrated [...]
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Stellenangebote Clinical Safety Associate Jobs bei Freelance.de

Job vor 9 Tagen gefunden Für Freelancer- Associate in Drug Delivery and Preformulation Sciences (f/m/d) • Basel Freiberuflich

MEHR

Freelancer Projekt- Associate in Drug Delivery and Preformulation Sciences (f/m/d) - Biopharmaceutics/ drug molecules/ German/ developing/ preclinical Project: For our customer a big [...] required. Tasks Responsibilities: As a (pre- ) formulation associate, you work with the preformulation project leader to plan and execute lab experiments for physico- chemical characterization of drug molecules, assessing their potential as medicines. You develop formulation concepts for pre- clinical studies across various administration routes in alignment with the respective scientist and perform formulation supplies and their analytical assessments independently. As a lab owner you are responsible for keeping the respective equipment operational, you organize maintenance services and follow all Roche guidelines and principles regarding Safety, Health and Environment. You use state of the art digital laboratory tools like electronic laboratory notebook and centralized data storage [...]
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Weitere Stellenangebote Clinical Safety Associate bei Jobleads

Job vor 4 Tagen gefunden

Laboratory Associate Regulated Bioanalysis

• Basel, Basel- Stadt

MEHR

[...] market and beyond. This position is located in the Regulatory Bioanalysis and Biosample Operations chapter within PS, which is accountable for developing efficient end- to- end (E2E) patient- centric biosample strategies ensuring maximum utilization of every sample comprising PK, immunogenicity, safety and PD (soluble target and biomarkers) endpoints and ensures assay readiness, data context enabling decision making and ultimately deliver robust and fit for purpose regulatory filings. The Opportunity This position is an excellent opportunity for a talented Laboratory Specialist to integrate into a dynamic lab team dedicated to the support of pre- clinical and clinical projects when complex bioanalytical assays or time- critical data are required. As part of the pRED organization you [...]

Job vor 4 Tagen gefunden Laboratory Associate Regulated Bioanalysis • Basel, Basel- Stadt

MEHR

Laboratory Associate Regulated Bioanalysis Roche fosters diversity, equity and inclusion, representing the communities we serve. When dealing with healthcare on a global [...] market and beyond. This position is located in the Regulatory Bioanalysis and Biosample Operations chapter within PS, which is accountable for developing efficient end- to- end (E2E) patient- centric biosample strategies ensuring maximum utilization of every sample comprising PK, immunogenicity, safety and PD (soluble target and biomarkers) endpoints and ensures assay readiness, data context enabling decision making and ultimately deliver robust and fit for purpose regulatory filings. The Opportunity This position is an excellent opportunity for a talented Laboratory Specialist to integrate into a dynamic lab team dedicated to the support of pre- clinical and clinical projects when complex bioanalytical assays or time- critical data are required. As part of the pRED organization you [...]

Job vor 6 Tagen gefunden

VP Clinical Development

MEHR

Job Description Job Title: VP Clinical Development- Oncology Tasks Responsibilities In this role, you represent Medicine at the International Multidisciplinary Evidence Teams and take clinical development [...] for the projects assigned. For example: definition of Target Product Profiles, Asset Evidence Plan, Pediatric Investigational Plan, core Clinical Trial Protocols, input to Project Analysis and Data Management Plan, Investigator Brochure, medical input to the Company Core Data sheet, Annual Safety Report/ IND Safety Reports, preparation for the Milestones Start of Development, Proof of Clinical Principle, Release of Full Development, Release [...] for studies that need to be conducted, and you provide input to Medical Affairs strategy documents such as Scientific Platform, Publication Plan, Product Maintenance and Optimization Summary. Furthermore, you review and approve publications within your project in collaboration with the associate Head of Medicine. As a VP Clinical Development, you: Author Investigator s Brochures, Asset Evidence Plans, Core Clinical Trial Protocols [...]

Job vor 6 Tagen gefunden Executive Director Clinical Development Führungs-/ Leitungspositionen

MEHR

Job Description Job Title: Executive Director Clinical Development- Oncology Tasks Responsibilities In this role, you represent Medicine at the International Multidisciplinary Evidence Teams and take clinical development responsibility for the projects assigned, including definition of Target Product Profiles, Asset Evidence Plan, Pediatric Investigational Plan, core Clinical Trial Protocols, input to Project Analysis and Data Management Plan, Investigator Brochure, medical input to the Company Core Data sheet, Annual Safety Report/ IND Safety Reports, preparation for the Milestones Start of Development, Proof of Clinical Principle, Release of Full Development, and [...] the need for studies that need to be conducted and provide input to Medical Affairs strategy documents such as Scientific Platform, Publication Plan, Product Maintenance, and Optimization Summary. You review and approve publications within your project in collaboration with the associate Head of Medicine. As an Executive Director Clinical Development, you: Author Investigators Brochures, Asset Evidence Plans, Core Clinical Trial Protocols, [...]

Job vor 14 Tagen gefunden

Clinical Development Medical Director

• Basel- Stadt Führungs-/ Leitungspositionen

MEHR

Leads the strategic and operational planning and management of the assigned clinical program (s) from an end- to- end clinical operations perspective. The Clinical Development Medical Director (CDMD) is responsible for leading [...] Driving execution of the assigned clinical program and/ or clinical trial in partnership with global line functions, assigned Global Trial Directors (GTDs) , and regional/ country medical associates, where applicable. Supporting (Senior) Global Program Clinical Head (GPCH) in ensuring overall safety of the molecule for the assigned section, and may act as a core member of the Safety Management Team (SMT) [...] and regulatory and clinical development processes. Previous global people management experience is preferred, though this may include management in a matrix environment. Final job title and associated responsibilities will be commensurate with the successful candidates level of expertise (Senior/ Director/ Associate) Accessibility and accommodation Novartis is committed to working with and providing reasonable accommodation to all individuals. If, because of a [...]

Job vor 14 Tagen gefunden Freelance Clinical Research Associate Freiberuflich Work-Life-Balance

MEHR

[...] a global full- service CRO dedicated to professional development and providing an excellent work- life balance, with a quality- focused, collaborative one- team culture. We are looking for a dynamic person to join our in- house team as a Freelance Clinical Research Associate for 0. 5 FTE. You will work on projects from our varied client base, ranging from small to big pharmaceutical, [...] periodic monitoring visits in the field and reviews at each visit accuracy, legibility, completeness, and quality of the Case Report Form (CRF) in compliance with the protocol, SOPs and ICH- GCP requirements in order to ensure data integrity and subject safety. Conducts source data verification and in- house review of clinical data and ensures timely resolution of data queries to guarantee [...]

Job vor 14 Tagen gefunden

Clinical Research Associate, sponsor dedicated

MEHR

Clinical Research Associate, sponsor dedicated The Clinical Research Associate will perform site activities for Phase I- IV studies operating as the main point of contact for the site during a study. Drive and execute monitoring plans, ensure site GCP compliance, write trip reports, resolve issues and facilitate open issue resolution, work on recruitment strategies, and monitor safety at the site. The CRA will conduct site qualification visits as assigned, site initiation visits and site training, routine monitoring [...]
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Job vor 14 Tagen gefunden Clinical Research Associate- Sponsor Dedicated

MEHR

Clinical Research Associate- Sponsor Dedicated ICON plc is a world- leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance [...] the site level with focused patient recruitment strategies and action plans. Identify site needs and site- related issues, escalate them and/ or initiate corrective actions when necessary, providing solutions for site staff to facilitate the clinical trial process. Ensures appropriate safety reporting as well as tracking and reporting of adverse events (AEs and SAEs) . Assist in preparing sites for audits, [...]

Job vor 14 Tagen gefunden

MSAT Associate Principal Scientist, Bioconjugates Process Expert for Capital Investment Project. . .

• Visp, Wallis

MEHR

MSAT Associate Principal Scientist, Bioconjugates Process Expert for Capital Investment Project 80- 100 (m/f/d) Today, Lonza is a global leader in life [...] be part of. The site in Visp, Switzerland is growing and for our Biologics organization, we are currently looking for a MSAT Bio Conjugates Process Expert. Lonza has a strong track record in the manufacturing of Bio Conjugates from early clinical to large scale commercial supplies. Our dedicated Protein Conjugation Plant facility (PCP) is recognized as a center of excellence for [...] Be responsible for permanent optimization of the project. By positive project evolution, be responsible for the execution of the assigned product/ project in the best possible time, quality, and cost, in compliance with the relevant laws, regulations, and guidelines regarding safety, quality, regulation, hygiene, and the environment from a MSAT point of view. Key Requirements: Master or PhD (preferred) in Bioconjugation, [...]

Job vor 14 Tagen gefunden Clinical Research Associate- Sponsor Dedicated Work-Life-Balance

MEHR

ICON plc is a world- leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government [...] the site level with focused patient recruitment strategies and action plans. Identify site needs and site- related issues, escalate them and/ or initiate corrective actions when necessary, providing solutions for site staff to facilitate the clinical trial process. Ensures appropriate safety reporting as well as tracking and reporting of adverse events (AEs and SAEs) . Assist in preparing sites for audits, [...]

Stellenangebote Clinical Safety Associate Jobs bei JobMagazin

Job vom 02.06.2024 Herman Medical Staffing GmbH

Anesthesia Supervisor needed in Saudi Arabia

• Saudi Arabia/ sonstiges/ weltweit Führungs-/ Leitungspositionen

MEHR

[...] the anesthesia supervisor supervises the activities of the state ofthe art cardiac anesthesia department is responsible for directing overseeing and facilitating the daily operation and performance of the anesthesia technicians preceptor mentor for anesthesia technicians will be responsible for ensuring clinical excellence in clinical practice by providing patients and their families the highest quality greatest safety and most efficient level of anesthesia care services leading hospital in saudi arabia is urgently looking for passionate and dedicated [...] to explore new culture and tradition while making a difference and bringing contributions through your specialized clinical and management skills knowledge and expertise in anesthesia technology essential requirements western educated trained and experienced healthcare professional bachelors degree in anesthesia technology associate of science degree in anesthesia technology program diploma in anesthesia technology or equivalent educational qualification in a related field required [...]
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Stellenangebote Clinical Safety Associate Jobs bei Job-Consult

Job vom 02.06.2024 Herman Medical Staffing GmbH Anesthesia Supervisor needed in Saudi Arabia • Saudi Arabia/ sonstiges/ weltweit Führungs-/ Leitungspositionen

MEHR

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