Senior Clinical Research Associate
2 giorni fa
Job DescriptionWe aspire to be the premier research-intensive biopharmaceutical company in the world.We demonstrate our commitment to patients and population health by increasing access to health care through far-reaching policies, programs and partnerships.
Today, we continue to be at the forefront of research to prevent and treat diseases that threaten people and animals – including cancer, infectious diseases, such as HIV and Ebola, and emerging animal diseases.Our purpose is to save and improve lives for generations.
Our strategy is simple: We follow the science.
The path to discovery is often unclear, but we are tireless in seeking solutions for some of the world's most difficult health challenges.The role is accountable for performance and compliance for assigned protocols and sites in a country.Under the oversight of the CRA manager or CRD, the person ensures compliance of study conduct with ICH/GCP and country regulations, our company's policies and procedures, quality standards and adverse event reporting requirements internally and externally.Acts as primary site contact and site manager throughout all phases of a clinical research study, taking overall responsibility of allocated sites.Actively develops and expands the territory for clinical research, finding and developing new sites.
Participates in internal meetings and workstreams as SME for monitoring processes and systems.Responsibilities include, but are not limited to:Develops strong site relationships and ensures continuity of site relationships through all phases of the trial.Performs clinical study site management/monitoring activities in compliance with ICH-GCP, Sponsor SOPs, Local Laws Regulations, Protocol, Site Monitoring Plan and associated documents.Conducts site visits including but not limited to validation visits, initiation visits, monitoring visits, close-out visits and records clear, comprehensive and accurate visit non-visit contact reports appropriately in a timely manner.Collects, reviews, and monitors required regulatory documentation for study start-up, study maintenance and study close-out.Communicates with Investigators and site staff on issues related to protocol conduct, recruitment, retention, protocol deviations, regulatory documentation, site audits/inspections and overall site performance.Identifies, assesses and resolves site performance, quality or compliance problems and escalates per defined CRA Escalation Pathway as appropriate in collaboration with CRA Manager, CRM, TA Head and CRD as needed.Works in partnership internally with GCTO country operations, finance, regulatory affairs, pharmacovigilance, legal and regional operations, HQ functional areas and externally with vendors and IRB/IECs and Regulatory Authorities in support of assigned sites.Contributes strongly to CRA team knowledge by acting as process Subject Matter Expert (SME), sharing best practices, making recommendations for continuous improvement and providing training as appropriate/required.Supports and/or leads audit/inspection activities as needed.Mentors/buddies junior CRAs on process/study requirements and performs co-monitoring visits where appropriate.QualificationsEducation and Minimum Requirements:Bachelor's or advanced degree in science and/or with relevant work experience in direct site management (monitoring) in bio/pharma/CRO.Required Experience and Skills:Fluent in Local Language and English (verbal and written) and excellent communication skills, including the ability to understand and present technical information effectively.Excellent understanding and working knowledge of clinical research, phases of clinical trials, current GCP/ICH country clinical research law guidelines.Excellent understanding of Global, Country/Regional Clinical Research Guidelines and ability to work within these guidelines.Demonstrated ability to mentor/lead.Hands-on knowledge of Good Documentation Practices.Proven Skills in Site Management including independent management of site performance and patient recruitment.Good IT skills (Use of MS office, use of various clinical IT applications on computer, tablet and mobile devices) and ability to adapt to new IT applications on various devices.Ability to understand and analyze data/metrics and act appropriately, also in a virtual environment.Experience with conducting site motivational visits designed to boost site enrollment.Performs root cause analysis and implements preventative and corrective action.Capable of mentoring junior CRAs on process/study requirements and is able to perform co-monitoring visits where appropriate.Behavioral Competency Expectations:Effective time management, organizational and interpersonal skills, conflict management, problem-solving skills.Able to work highly independently across multiple protocols, sites and therapy areas.High sense of accountability/urgency.
Ability to set priorities and handle multiple tasks simultaneously in a changing environment.Works effectively in a matrix multicultural environment.
Ability to establish and maintain culturally sensitive working relationships.Demonstrates commitment to Customer focus.Positive mindset, growth mindset, capable of working independently and being self-driven.We are proud to be a company that embraces the value of bringing diverse, talented, and committed people together.
The fastest way to breakthrough innovation is when diverse ideas come together in an inclusive environment.
We encourage our colleagues to respectfully challenge one another's thinking and approach problems collectively.
We are an equal opportunity employer, committed to fostering an inclusive and diverse workplace.Employee Status: RegularRelocation: No relocationVISA Sponsorship: NoTravel Requirements: 75%Flexible Work Arrangements: RemoteShift: Not IndicatedValid Driving License: YesHazardous Material(s): n/aJob Posting End Date: 12/21/2024*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date.
Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.Requisition ID: R323804 #J-18808-Ljbffr
-
Senior Clinical Research Associate
2 ore fa
Lazio, Italia Buscojobs A tempo pienoAbout this role TFS Health Science is a leading global, mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service capabilities, resourcing, and functional service (FSP) solutions.The Clinical Research Associate (CRA) is...
-
Senior Clinical Research Associate
2 settimane fa
Lazio, Italia Tfs Healthscience A tempo pienoAbout this role TFS HealthScience is a leading global, mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey.Our expertise includes full service-capabilities, resourcing and functional service (FSP) solutions.The Clinical Research Associate (CRA) is...
-
Senior Clinical Research Associate
1 giorno fa
Lazio, Italia Buscojobs A tempo pienoAbout this role TFS Health Science is a leading global, mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service capabilities, resourcing, and functional service (FSP) solutions. The Clinical Research Associate (CRA)...
-
Clinical Research Associate
1 mese fa
Lazio, Italia Tfs Healthscience A tempo pienoCRA Italy - 0.2/0.4 FTE - FREELANCE About this role TFS Health Science is a leading global, mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey.Our expertise includes full service-capabilities, resourcing and functional service (FSP) solutions The...
-
Lead Clinical Research Associate
3 settimane fa
Lazio, Italia Ora A tempo pienoPOSITION TITLE: Lead Clinical Research AssociateDEPARTMENT: Ora EuropeLOCATIONS: Poland, Spain or ItalyOra Values the Daily Practice of … Prioritizing Kindness * Operational Excellence * Cultivating Joy * Scientific Rigor At Ora, we are building the future of ophthalmic clinical research. As the world's leading full-service ophthalmic drug and device...
-
Lead Clinical Research Associate
2 settimane fa
Lazio, Italia Ora A tempo pienoPOSITION TITLE: Lead Clinical Research Associate DEPARTMENT: Ora Europe LOCATIONS: Poland, Spain or Italy Ora Values the Daily Practice of … Prioritizing Kindness * Operational Excellence * Cultivating Joy * Scientific Rigor At Ora, we are building the future of ophthalmic clinical research.As the world's leading full-service ophthalmic drug and device...
-
Senior Clinical Research Associate
5 giorni fa
Lazio, Italia Merck Gruppe - Msd Sharp & Dohme A tempo pienoJob DescriptionWe aspire to be the premier research-intensive biopharmaceutical company in the world.We demonstrate our commitment to patients and population health by increasing access to health care through far-reaching policies, programs and partnerships. Today, we continue to be at the forefront of research to prevent and treat diseases that threaten...
-
Associate Director
2 mesi fa
Lazio, Italia Msd A tempo pienoWe aspire to be the premier research-intensive biopharmaceutical company in the world. We demonstrate our commitment to patients and population health by increasing access to health care through far-reaching policies, programs, and partnerships. Today, we continue to be at the forefront of research to prevent and treat diseases that threaten people and...
-
Research Associate
1 mese fa
Lazio, Italia Randstad Italy A tempo pienoSei un ricercatore appassionato di biologia e chimica con esperienza nel campo della caratterizzazione strutturale?Se sei alla ricerca di un'opportunità stimolante e di un'esperienza in un ambiente dinamico e innovativo, questa potrebbe essere la tua occasione!Randstad Italia spa , divisione Pharma di Roma Tiburtina, ricerca per un'azienda leader nel...
-
Research Associate
3 giorni fa
Lazio, Italia Buscojobs A tempo pienoRESEARCH ASSOCIATE Settore: manifatturiero & produzione Categoria: Tecnici specializzati, qualità Orario di lavoro: Full Time Contratto: Somministrazione Numero posti: 1 Luogo di lavoro: Roma Sei un ricercatore appassionato di biologia e chimica con esperienza nel campo della caratterizzazione strutturale? Se sei alla ricerca di un'opportunità...
-
Executive Account Director, Business Development
1 settimana fa
Lazio, Italia Thermo Fisher Scientific A tempo pienoAt 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...
-
Lazio, Italia Thermo Fisher Scientific A tempo pieno```html 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...
-
Lazio, Italia Https:Www.Energyjobline.ComSitemap.Xml A tempo pienoAt 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...
-
Lazio, Italia Thermo Fisher Scientific A tempo pieno```htmlAt 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...
-
Senior Research Fellowship Program
3 settimane fa
Lazio, Italia European Institute Of Policy Research And Human Rights Sia A tempo pienoApplications are now open for the Senior Research Fellowship followed by 8 weeks Online Internship at the European Institute for Policy Research and Human Rights.About the Program Our renowned online Career Rejuvenator SUPERProgram is tailored to help students and professionals enhance their research and academic writing skills.This flexible internship is...
-
Research Associate- Qc
3 settimane fa
Lazio, Italia Randstad A tempo pienoSei un ricercatore appassionato di chimica con strutturata esperienza cromatografica e elettroforesi proteica?Sei alla ricerca di un'opportunità stimolante e di un'esperienza in un ambiente dinamico e innovativo, questa potrebbe essere la tua occasione!Randstad Italia spa , divisione Pharma di Roma Tiburtina, ricerca per un'azienda leader nel settore...
-
Categorie Protette
5 mesi fa
Lazio, Italia Intellera Consulting A tempo pienoIntellera Consulting S.p.A. nasce ad agosto 2021 dal Public Sector di PwC Business Services Italia ed è, per volume d'affari, la prima azienda di consulenza italiana specializzata nel settore pubblico.Intellera si pone al centro e a sostegno della trasformazione ed evoluzione culturale, organizzativa e tecnologica di Enti pubblici e anche privati.Le persone...
-
Associate Counsel, Legal Contracts
4 settimane fa
Lazio, Italia Thermofisher A tempo pienoWork ScheduleOtherEnvironmental ConditionsOfficeJob DescriptionAt 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...
-
Corporate Counsel, Clinical R&D Legal
1 settimana fa
Lazio, Italia Buscojobs A tempo pienoAbbVie’s Clinical R&D Legal team is seeking an experienced attorney to partner with, and provide strategic legal and business advice to, the company’s global R&D organization. The Corporate Counsel, Clinical R&D Legal, will be an integral part of a solutions-oriented team of attorneys and paralegals that supports advancement of AbbVie’s pipeline and...
-
Corporate Counsel, Clinical R&D Legal
1 settimana fa
Lazio, Italia Buscojobs A tempo pienoAbbVie's Clinical R&D Legal team is seeking an experienced attorney to partner with, and provide strategic legal and business advice to, the company's global R&D organization. The Corporate Counsel, Clinical R&D Legal, will be an integral part of a solutions-oriented team of attorneys and paralegals that supports advancement of AbbVie's pipeline and delivery...