EPM Scientific’s Post

Struggling to find top-tier Clinical Operations talent for your projects across Europe? 🌍💼 In the dynamic world of clinical research, agility is key. As a seasoned Clinical Operations professional with a rich tapestry of experience in freelance contracting, I understand the pulse of this industry and the importance of having the right people on board. 🚀 I've had the privilege of leading and collaborating on diverse clinical trials, ensuring they run smoothly, efficiently, and in compliance with stringent regulations. My journey has taken me across various European landscapes, giving me a unique perspective on the nuances of regional clinical practices and the ability to adapt swiftly to different regulatory environments. 📊🔬 If your Clinical Research Organisation is on the lookout for someone who can hit the ground running, manage cross-functional teams, and drive your trials towards success, let's connect. I offer the flexibility of freelance contracting with the commitment of a full-time advocate for your clinical objectives. 🤝 Let's discuss how my expertise can align with your project needs and elevate your operational capabilities. Drop a comment, send a DM, or simply hit 'Like' if you're interested in a collaboration that bridges the gap between talent and opportunity. 🌐✨ #ClinicalOperations #FreelanceExpertise #ClinicalResearchEurope #HRS #Science

Navigating the CRA Talent Maze Finding top-notch CRAs is no small feat! As a Clinical Research Line Manager, you know the stakes are high. That's why I'm here - to connect Europe's best with your visionary projects, on terms that flex with your needs: freelance or contract Having worked alongside some of the brightest in the field, I've seen firsthand the impact a skilled CRA can make. Their meticulous attention to detail, unwavering commitment to compliance, and their pivotal role in driving forward clinical research are just irreplaceable. But the quest for such candidates can feel like searching for a needle in a haystack So here's my proposition: Let's streamline this search. With a robust network across Europe's clinical research landscape, I bridge the gap between your project demands and the freelancers who can meet them head-on. It's about precision pairing - ensuring that every professional I connect to your team isn't just a good fit but the right fit Say goodbye to endless CV sifting and hello to a tailored selection of candidates ready to deliver. With expertise spanning across the EU, I navigate the complexities of clinical standards, local regulations, and varied healthcare systems to secure the freelance CRAs who aren't just qualified - they're primed to excel #ClinicalResearch #CRA #FreelanceOpportunities #ContractWork Let's reshape the future of clinical trials together. Drop a comment, connect, and let the collaboration begin! #HRS #Science

Navigating the CRO landscape? As Europe's CRO sector surges ahead, the hunt for top-tier freelance and contract talent is fiercer than ever. But what if I told you there's a goldmine of opportunity just waiting to be tapped? Having worked with industry leaders, I bring a fresh perspective to your clinical trials. I'm all about sharpening that competitive edge with strategic insights and flawless execution. Think less jargon, more action! I'm seeking collaboration with innovative CROs across Europe. Let's blend your scientific prowess with my operational agility to drive your projects to new heights. Together, we can shape the tapestry of groundbreaking medical advancements! Drop a message if you're on the lookout for dedicated expertise, or tag someone who is! Let's connect and explore a partnership that propels us forward. #CRO #FreelanceTalent #ClinicalResearch #Science #HRS

Navigating the EMEA CRO landscape? In the swiftly evolving world of Clinical Operations, Medical Affairs, and Biometrics, staying ahead means securing top-tier freelance talent at a moment's notice. As specialists in providing freelance contractors, we offer the agility and expertise your projects demand. Building a successful project team isn't just about filling seats. It's about finding minds that breathe life into your groundbreaking initiatives. Whether it's a clinical trial or a vital data analysis, each freelance professional brings a unique skill set and adaptability to your enterprise. We understand that in the realm where precision is non-negotiable, the right staffing decisions can catapult your operations from routine to revolutionary. How do we do it? By fostering partnerships rooted in trust and performance, ensuring our contractors not only match your needs but exceed them. Because every patient counts. Because every data point matters. To the CROs in EMEA: What is the key challenge you face in assembling your dream team for critical projects, and how can we unlock that door together? #CRO #ClinicalOperations #MedicalAffairs #Biometrics #EMEA #FreelanceTalent #HRS #Science

MedComms Advent Calendar, Day 1: Patient Information Leaflets (#PIL) & Informed Consent Forms (#ICF) PILs are those handy leaflets that come with your medications, explaining what they do, how to take them, and the side effects to watch out for. Then there's ICFs - the forms you sign before a treatment or procedure. They make sure you know exactly what's happening, the risks, and the benefits. It's all about making choices that you're comfortable with. Both PILs and ICFs are all about keeping you informed and involved in your healthcare journey. 🌟🌟 Welcome to my new seasonal series - the #MedCommsAdventCalendar, where I'll highlight different types of materials I've had the privilege of working with over the past year. Hopefully, I will have the chance to do it again in 2024!😉😉 – – – – – – – ✍ I write about #MedicalTranslation and #MedicalWriting, sharing tips and strategies for freelancers and clients. 🔵 Follow my hashtag #YourPortuguesePatientPartner for insights, updates, and behind-the-scenes glimpses of my work. Plus: #️⃣ MedCommsFAQ for questions frequently asked by clients in medical communications. Share your answers! #️⃣ FridayClinicalCorner for a brief breakdown of clinical research terms from my work week. Join me every Friday! #️⃣ MondayMedCommsTip for weekly bite-sized recommendations on crucial aspects of medical writing and translation. Start your week right! 🟢 Follow or Connect with me! (Don't forget to hit the 🔔 at the top of my profile.) 👉 Now running the #MedicalTranslationMentoring program.

🔍 Exploring the Benefits of Medical Affairs Senior Interim Contractors! 💼 Looking to enhance your Medical Affairs team's capabilities? Consider the value that senior interim contractors can bring to the table: 🔹 Immediate Engagement: Leverage MSLs with specialized knowledge and networks for seamless KOL engagement from day one. 🔹 Strategic Support: Tap into the expertise of Medical Affairs leaders to mentor and coach Field Medical on effective KOL engagement and devise comprehensive launch strategies. 🔹 Digital Innovation: Initiate digital strategies with pilot projects designed and implemented by Medical Affairs experts for future scalability. 🔹 Project Flexibility: Enjoy the flexibility of engaging contractors based on your project needs – whether full-time, part-time, or for specific durations. With Medical Affairs Interim Contractors, you can drive your business forward without the commitment of additional headcount. Let's discuss how these experts can add value and propel your projects to success! 💡💪 Reach out to me at [email protected] Healthcare Professionals Group #MedicalAffairs #InterimContractors #HealthcareInnovation 🚀👩⚕️

✳ Today, I would like to explore the key components of creating a robust Clinical Evaluation Report (CER) for submission to the NMPA! ✳   The content of the CER should include the following elements:   1️⃣ Product description and R&D background: This section includes the basic information, scope, and R&D background of your medical device, as well as the working principle, existing diagnostic or therapeutic methods and clinical applications. The relationship of the device to existing diagnostic or therapeutic methods, clinical efficacy and intended clinical benefits should also be addressed.   2️⃣ Scope of the clinical evaluation: This section describes the scope of the clinical evaluation.   3️⃣ Clinical evaluation approach: Explain your clinical evaluation approach (see one of my previous posts for more information).   4️⃣ Analysis and evaluation with the clinical data of medical devices of the same type: This section should provide a basic description, demonstration of equivalence, and summary, evaluation, and analysis of the clinical data of the equivalent device. See my previous post for more information.   5️⃣ Conclusion: Summarize the results and demonstrate the safety and performance of your medical device.   6️⃣ Clinical evaluators: The expertise and roles of the evaluators involved.   7️⃣ Other issues to be addressed (if applicable): Address any other relevant issues.   ❗ What is your CER’s goal? To demonstrate the safety and intended performance of your medical device.❗ Keep this in mind while preparing the CER. With a well-structured clinical evaluation report that meets NMPA requirements, you will pave the way for successful market entry in China. ❓ What challenges have you faced in preparing a Clinical Evaluation Report for NMPA submission ❓   ------------------------------------------------------------------------------------- If you are looking for a freelance Medical Writer, writing clinical evaluation documents for medical devices that secure compliance with regulatory requirements, please contact me 📨 .    #MedicalDevices #RegulatoryCompliance #NMPA #ClinicalEvaluationReport #ClinicalEvaluation #RegulatoryWrititng #MedicalWriting

Ever wondered what it's like to transition from a Medical Doctor's traditional path into the world of Freelance #MedComms Consultancy? In our latest article, Dr Ana Hutanu shares her experience of transitioning into the role of a Freelance MedComms Consultant, outlining the key advantages of this role, from increased flexibility to the opportunity to build meaningful client relationships: https://buff.ly/3XfZuCm #freelancejobs #medicalcommunications #medcommsjobs #consultancy

The medical field is one of the most heavily regulated industries and relies on strict adherence to many policies, procedures, and other documentation. Ensuring compliance is tough, but clear communication can make all the difference. Click the link to learn more about the benefits of medical documentation services today! https://lnkd.in/ekTtWCNw #medical #documentation #services #technicalwriting

Alert: venting post! Please tell me I am not the only one who spends a ton of time taking care of the medical needs of an elder family member. Last week, I spent close to 15 hours; this week, it will be around 12. I can do it because I work for myself, and as a medical writer, I am somewhat familiar with medical terminology, so I don't feel that lost. How does the rest of the world do this? Like people with full-time jobs who are not MDs and not familiar with medical jargon? I just spend 2.5 hours on the phone simply scheduling medical appointments. Can this be outsourced?