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- CADRE TRANSATLANTIQUE: TRANSFERT DE DONNÉES CLINIQUE
- Impact du règlement européen sur l’étude phase IV
- Attaché de recherche clinique oncologie (H/F) – Clermont-Ferrand
- Technicien d’étude clinique en Oncologie (H/F) – Bordeaux
- Que diriez-vous d’un Battle de la recherche clinique
- When a company uses anonymisation, does the GDRP apply to it?
- When the sponsor requests a pre-screening list, is it possible to initial the patient’s name before the patient has signed an informed consent?
- GDRP : Can the DPO be based outside the European Union?
- Can a patient request the deletion of data from his/her medical record?
- Should clinical study technicians take the steps related to the GDRP ? Who should carry out these procedures?
- GDRP : Can an impact assessment be made after once the processing has begun?
- Is there an GDRP certification? How can I prove that my company is GDRP compliant?
- Who must notify the CNIL of a violation?
- GDRP/clinical research: Do patients have the right to retrieve their data in order to transfer it to a concurrent company?
- How do I become a DPO (Data Protection Officer)?
- Comprendre les textes législatifs ou règlementaires en recherche clinique
- Informed Consent Forms (ICF) and Patient infrormation Sheet: 10 Tips to acheive your goals
- Which profession is the most suitable for a PhD?
- The earthquake: Invalidating the Privacy Shield and clinical research (Now, what?)
- Clinical Research: How format can change a CRF presentation for the better?
- 2 years of experience as CRA, how to quickly become a project manager
- VLOG Forum Biotechno Paris 2020
- This is the first monitoring visit what is your priority?
- How can I be sure that the CRA job is for me ?
- Strategy : What immediate evolution for an CRA ?
- Interview de Jules : Le métier d’ARC?
- How to train in different pathologies when you are a Clinical Study Coordinator at the hospital?
- Challenge #30: Zen GCP audit!
- Challenge # 29: Tips from an experienced ARC !!!
- Challenge #28:What are the essential tools for quality monitoring?
- Challenge #27: My patient was enrolled, he did not have the criteria, what should I do?
- Challenge #26 : Fraud in clinical trials, what to do?
- Challenge #25 : My patient received the wrong treatment or the wrong dose, What should I do?
- Challenge #24 : Can I retrieve ethnic data from the CRF in France?
- Challenge #23 : L’ALCOAC, comment l’appliquer dans le monitoring?
- Challenge # 22: There is no such thing as the lost of sight!
- Challenge # 21: Centrifuge, refrigerator, freezer in clinical studies, what should you check?
- Challenge # 20: What to check when signing an informed consent form?
- Challenge #18: In France, should you ask for the diplomas of the investigators?
- Challenge # 16: Essential document: What should your investigator’s CV contain?
- Challenge # 15: Monitoring visit: Laboratory kits, What to check?
- Challenge # 14 Monitoring visit: The investigator site file, What to check?
- Challenge # 13 Do I have the right to retrieve the patient’s initials via the CRF?
- Challenge # 12 Anonymization and pseudonymization? What is the difference?
- Challenge # 17: Monitoring at the pharmacy, what to check?
- Challenge #11 The person who signed the consent is a resident physician. What to do?
- challenge # 10 The doctor signed the consent, he is not on the delegation log
- challenge # 9 I am replacing a CRA permanently, What to check?
- challence # 8 a SAE during the weekend. the declaration did not take place within 24 hours. What to do?
- Challenge # 7 No AE grade and no link to the product under study in the medical file. What to do?
- Challenge #6 My patient’s medical record is lost! What can I do?
- Challenge # 5 Multiple nurses are working on my clinical study, I don’t have their CV !!
- Challenge # 4 The concomitant treatments are missing in the source file, what to do?
- Challenge # 3 The medical file is in electronic version, What should I pay attention to?
- Challenge # 2 My investigator refuses to put certain adverse events in the CRF
- Challenge # 1 – Do the investigator and the patient have to sign the consent on the same day?
- Mon premier entretien d’embauche collectif!
- TEC freelance avec 1 an d’expérience, est ce possible?
- Je cherche un stage de master 1, les CROs ne me répondent pas, que faire?
- Trophée afro-créoles 2019: Lauréate Innovation et société
- Podcast: La priorité d’une première visite de monitoring
- “Interview: La coiffure afro impactera-t-elle sur votre embauche
- Podcast: CRF papier ou électronique à présenter
- Regarde notre nouvelle vidéo « collaborActeurs ».
- How do I finance my CRA training?
- J-2 de la présentation de notre vidéo Corporate
- J-4 du lancement de notre vidéo Corporate Pharmaspecific
- What is CRA’s clinical research and business ?
- How do I find an CRA position in my area?
- How to become an CRA if you have a foreign diploma ?
- Pourquoi as-tu besoin d’un coaching pour trouver un emploi ?
- How can you find an CRA job when you have no experience at all ?
- How to find a position in CRO or in a pharmaceutical laboratory ?
- Where to find companies to apply ?
- J’ai le statut d’étudiant étranger, difficile pour moi de trouver une embauche en France
- CPF: le dispositif de formation pour les salariés
- Comité d’éthique à l’étranger, la différence avec la France
- Connaissez vous Les Bonnes Pratiques De Data Management?
- Soumission dossier au CPP: Utilisez la nouvelle plateforme CNRIPH
- I have a Ph.D. in biology, the employees won’t hire me
- Case study SAE unreported for several weeks, what to do ?
- Small or large CRO, which strategy to choose ?
- Do I pay so much for CRA training?
- Strategy : to become a freelancer, Good or Bad Idea ?
- Strategy: CRA CRO or CRA presta, what is the difference/benefit?
- Case Study – Disaster, Consent is Lost !
- Le Canada : l’envie d’avoir une expérience de travail Internationale
- Mon Investigateur est exécrable que faire ?
- I can’t find a CRA job, I’m stressed, what should I do?
- La journée type d’un technicien en étude clinique
- Votre mémento est disponible, commandez le dès maintenant
- ANNONCE : Troisième édition du mémento sur les recherches cliniques
- Bookez votre agenda du 31 Janvier 2019. The place to be
- Failure to complete the Master’s degree in clinical research, what can I do ?
- Arrivée imminente du mémento sur la recherche biomédicale
- I’m afraid of failure!
- Voici quelques histoires malchanceuses d’une ARC
- Protected: SONDAGE SALAIRE – RECHERCHE CLINIQUE – 23 AVRIL 2018 – MAJ 19Jan19
- En 2018, à combien le salaire en recherche clinique
- Le consentement des mineurs en recherche clinique
- Double aveugle (Double Blind) ou double insu
- La fin de traitement dans la recherche clinique
- Motiver son équipe à donner le meilleur d’eux-mêmes
- Au cœur du métier d’attaché en Recherche Clinique
- 5 points sur la négociation avec les centre d’investigation
- Délégation log : un outil de délégation de tâches
- Que signifie : SUSARS, CIOMS, Medwatch, VAERS
- La chaine France O invite Vanessa Montanari
- Pharmaspecific training est officiellement ouvert!
- Comité de surveillance et de suivi de données (DSMB)
- Partagez votre propre expérience en tant qu’ARC
- CRF – eCRF : L’utilité d’un cahier d’observation papier ou électronique
- Bonne nouvelle, le nouveau site est dans les starting-blocks!
- Food and Drug Administration 1572 : quand l’ utiliser?
- Rôle de l’investigateur coordinateur en recherche clinique
- Réponses aux questions de Ines, Laetitia, Jalila et Nathalie
- Vendredi 15 Décembre: Invitation pour un escape Game à Paris
- C’est décidé, je pars au Canada ! : Interview d’un expatrié
- Documentaire sur la recherche clinique : First in Human
- Ecoutez l’interview de Vincent DIEBLOT, directeur du F-CRIN
- CRO (Contract research organization)
- ANSM: agence d’évaluation, d’expertise et de décision
- Réunion en recherche clinique gratuite à ne pas manquer !
- Photo or no photo on my CV ?
- Qu’est ce qu’on entend par effet indésirable?
- Le contenu des étiquettes requis par la Loi
- Guide de bonnes pratiques de fabrication
- Les points à revoir dans un contrat d’essai clinique
- Remboursement des prises en charge liés à la recherche
- L’appel aux patients: Quand et comment parler au patient
- Watch out for your messages on Linkedin
- Médical Science Liaison (MSL): les réponses de François
- The 3 priorities not to be forgotten in monitoring.
- SOciety of Clinical Research Associates (SOCRA), nous sommes membres
- Think about recruitment companies
- I can’t find a job in CRA position, why is that ?
- What level of education is required to become a CRA ?
- Why to keep in touch with former managers ?
- Conseils pratiques pour bien manager une équipe d’ARC
- The Best Time to Find a CRA Job
- The 3 things missing from your CRA CV
- D’ici 10 ans: évolution professionnelle des ARCs et TECs
- Tout savoir sur le métier d’ARC, regardez cette vidéo
- SOUVENIR, SOUVENIR…LA JOURNEE DE LA RECHERCHE CLINIQUE 2017
- Pharmaspecific : Poste d’ARC Guadeloupe/Martinique, Octobre 2017
- Assemblée plénière du 26 juin 2017 organisée par le Comité de Patients en Recherche Clinique en Cancérologie
- Des questions à poser? Medical Science Liaison vous répondra
- Les comités de surveillance en Recherche Clinique
- Est-ce que ton certificat d’assurance est conforme ?
- l’e-CRF : un outil essentiel et incontournable pour les ARC
- Jooble: une plateforme de recherche d’emploi 2.0
- Comment écrire de SUPER procédures opératoires standardisées?
- En quoi consiste la nouvelle méthodologie de recherche MR-003
- Partie 2 : La vigilance dans les essais cliniques
- Se former ou suivre un stage pour devenir ARC
- Jardé law, in practice: The IRB and the ANSM
- Q&A (3): Contract in CR, Freelance, medical monitor
- Testimonial of Laura, The challenge 2016 (mentoring)
- My answers to your questions on CRA profession (Part 2)
- My answers to your questions on the CRA profession (Part 1)
- My challenge 2017
- Christmas Q&A: Chapter 2 (Part 2)
- Christmas Q&A: Chapter 2 (Part 1)
- Q&A – Chapter 1
- The 4 Values to Succeed as a CRA
- Christmas FAQ [Completed]
- Single contract, the record!
- Congratulations to the winner of the Crazy Pic!
- Monitoring at the pharmacy, the pillars of success!
- Collabore avec Pharmaspecific en tant qu’apporteur d’affaires
- What is ISO9001 certification ?
- What is ISO9001 certification?
- Un ARC et le paysage asiatique d’essais cliniques
- I cannot organize my workflow, how do I?
- Is it possible to switch from CRC to CRA-CRO ?
- Zen CRA, how to improve your well-being at work?
- Pharmaspecific goes green
- 20 Septembre: anniversaire du Blog de la Recherche Clinique
- How to attract promoters and CROs?
- Clinical site coordinator, how to avoid protocol deviations in my center?
- Mentoring: Good news!
- I crumble under the mails, how to get out alive?
- This is hell, I resume my colleague’s studies!
- Help, I have a consent to monitor!
- Hospital CSC or CRO CSC ?
- The ALCOA, ALCO … WHAT?
- At the intersection of clinical research actors
- Are you freelance? Collaborate with Pharmaspecific!
- How to choose a provider in clinical research?
- I need a helping hand!!!
- View the 2nd edition of the free eBook Mosio! We participated in drafting!!
- Role and tasks of a clinical data manager
- How to improve the recognition of the CRC profession ?
- 8 essential points for a comprehensive monitoring report
- 5 tips for a successful CRA interview
- How to succeed your implementation visit?
- The best clinical research conferences of TED.com
- Mentoring of our winner : Laura
- CRA and CRC, 7 practical tips on SAE …
- Why are CROs reluctant to hire hospital CRAs ?
- Mentoring session with Marthe, CRA trainee
- Mentoring session with Jonathan, future CRA
- 5 things to know when you’re a CRA
- It is decided, I am going to Africa!
- How the transverse management will change your CRA and CSC work?
- Accident in clinical trials and compensation for victims
- I am co-author of a clinical research memento, come help us!
- How to prepare an audit without stress?
- Medical Science Liaison, a conversion for the CRAs?
- Les recettes d’une visite de monitoring réussie
- Le « SMO » : Site Management Organization, qu’est-ce que c’est ?
- The 2014 European Directive
- The 2016 challenges
- After the MR-001, the MR-002…
- Invalidation of Safe Harbor, what to do?
- Oncology Planet
- The ICH on the fingertips
- A Resume in order to be recruited
- How to organize yourself when you are a “home-based” CRA?
- The whole truth about the CRA profession
- You are CRA and / or PM, how to get a pay raise?
- All I need to know to become a CRA
- Succeeding his telephone interview
- The 3 best smartphone apps for CRA
- Electronic informed consent
- The Cooperator Groups in Oncology (CGO): who are they?
- The “perfect” FDA 1572 form
- Your study : BMR or routine care?
- Clinical Research: alert of the public opinion and Senators
- What do investigators expect from CRA and Site Study Coordinator?
- 10 essential tools for a monitoring of quality!
- Clinical research and medical devices, how to go about it?
- Project manager and CRA manager, let’s explain the words!
- The patients committee in clinical research, a definite advantage for promoters
- CRA and CRC, how to choose the right Job?
- The risk-based monitoring: a new method for quality control?
- Clinical trials insurance, how to choose it well?
- Our best tips to recruit investigators effectively
- Always with my “Dorosz”
- All recipes to boost inclusions
- Drop outs, don’t exist!
- The MR-001, what is it and how to respect it?
- Small CROs, where to find them to apply?
- Keys for a successful closure visit!
- How to use Linkedln, Twitter and Viadeo to find a CRA job?
- How to succeed in reconciling personal and professional life when one is CRA monitor?
- “It’s decided I’m going to England”: Interview with an expatriate CRA
- Information note and informed consent, the main points
- 5 trick questions to be absolutely prepared for your CRA interview
- The patient reimbursement: who is charge and how does it work?
- Profession CRA sheet: My testimony at the APEC (French Association for the executives employment)
- What changes to the CRA and SSC profession in France in 10 years?
- How to communicate effectively with your investigator, your CRC and your pharmacist?
- Memento of biomedical research relating to a medicinal product for human use – Laurence Culine
- Top 5 ways to find a CRA job
- Remote monitoring…the evolution of the Clinical Research Associate profession (CRA)
- The 10 Commandments of clinical project manager
- Hospital single contract: real benefit to the French clinical research?
- Spoken English: 3 tips, at low cost
- The Top 10 job websites for CRAs
- How to become a freelance CRA ? (Part 3)
- How to become freelance ARC ? (Part 2)
- How to become a freelance CRA? (Part 1)