Annabelle Lewis’ Post

Is your LinkedIn profile working hard enough for you? Your profile is your digital CV and often a recruiter’s first impression, so it's important to invest time in optimising it. Let’s break it down: Headline • You have 220 characters to craft a compelling headline. Be precise; include your current role and key skills. e.g. Clinical Project Manager | Oncology Specialist Summary • Use the first three lines to grab attention, as they are visible without clicking 'See more...'. • Here, you want to highlight your expertise, career goals, and your unique value proposition. e.g. Passionate Clinical Research Professional with over 5 years of experience in managing complex clinical trials. My mission is to drive innovation in healthcare through meticulous research and unwavering commitment to patient safety. Experience • This is where you showcase your achievements. • Focus on results and impact rather than just listing responsibilities. • Use Feature = Result e.g. Managed a Phase III oncology trial, resulting in a 25% increase in patient recruitment compared to previous studies. Other Tips: • Highlight your skills and seek endorsements from colleagues. • Use relevant industry keywords to enhance visibility.

Big CRO vs Small CRO What's the difference If you're considering a Career in Clinical Project Management Here's What You Need to Know! 🟢 At Large CROs: • You'll dive deep into specific therapeutic areas or trial phases. • PMs manage large-scale trials spanning multiple sites and diverse patient populations. • You'll have access to advanced tech and standardized processes due to the scale. • PMs typically engage with high-profile pharmaceutical clients and navigate complex global regulations. • There is more of a focus on project management aspects due(overseeing tasks) to varied roles within the organization. 🟢 At Small CROs: • PMs wear multiple hats, handling diverse tasks and engaging directly in various trial aspects. • You're expected to adapt swiftly to changing project needs and market demands, demanding agility and resourcefulness. • PMs Directly liaise with clients, offering personalized and direct interactions. • You typically have more of an opportunity to gain a comprehensive understanding through exposure to various tasks. • Resources are often more limited, so creative problem-solving is a key attribute to highlight when interviewing Neither is better or worse. It depends on the preference Choose wisely based on your preference for specialization, adaptability, and direct client engagement. Your choice shapes your clinical project management journey! ________________ 👋 Looking for tips, tricks, and resources to help with your job search? → Follow #CGATips → Visit my profile page and hit [Follow] → Smash the 🔔 to be notified when I post → Subscribe tomy YouTube Channel for Weekly Video Tips → Need help? DM me! #ClinicalResearch #CareerPathways #ProjectManagementSuccess

Friends, Colleagues, and Fellow Travelers on the road of life, As some of you may know, Kite Pharma recently made the difficult decision to lay off nearly 7% of their global workforce. Unfortunately, the hybrid in-house Project Management Org/Talent Accelerator that I led was eliminated as part of this change. As such, I now find myself one of many who are in search of new opportunities in a very difficult job market. For those of you who might not be fully acquainted with my background: over the past 10 years, I have grown into a highly skilled Technical Operations leader, with strong management experience in Supply Chain, Quality Operations, and Project/Portfolio Management. Augmenting this is an additional 3 years in Clinical Operations working with both product and sponsor to ensure optimal study execution. Here's just a few of my career highlights to date: -         Spearheaded a Tech Ops focused business rotation dept in the Cell Therapy space (Supply Chain, Quality, Process Dev, MSAT, Biz Ops, and more), mentoring and developing over a dozen junior Project Managers with international impact -         Designed, developed, and deployed an enterprise-wide Order Management System and companion Lot Release Prioritization “SWAT team”, leading to the elimination of a Drug Substance backlog of over 100 lots and the reduction of the Drug Product lot backlog by greater than 50% -         Headed up all Commercial and Clinical planning and operations activities for Dupixent, a Regeneron blockbuster program. This included leading collaboration planning and threat mitigation efforts with ex-US strategic partner Sanofi -         Collaborated with a team of SME’s and PM’s to rapidly bring Regeneron’s life-saving REGN-COV2 anti-COVID monoclonal antibody treatment to market under an Emergency Use Authorization My humble request to all of you is this: if we’ve worked together in the past and you were impressed with the quality or character of my work, would you please consider authoring a recommendation for me via my LinkedIn page? It could go a long way towards helping me earn my next opportunity to make an impact. Additionally, if you should become aware of any open opportunities that you think might be a good fit at companies where you still maintain contacts, would you please consider making a connection? I am currently in search of roles from the Director to Senior Manager level, in the realms of Supply Chain, Quality, and Project/Portfolio Management. I would also be very excited to discuss any Relationship Management/Business Development positions as well. Thank you all in advance for your continued support through these difficult times. I look forward to our future collaborations!

As a Clinical Operations Manager, I am privileged to play a key role in driving clinical trials forward, providing new indications and delivering robust scientific evidence to advance medical research. The Importance of Clinical Operations Management: Clinical operations management is at the heart of successful clinical trials. It encompasses planning, organizing, directing, and controlling the resources and processes necessary to conduct a study. The Pillars of Our Mission: Planning and Coordination: Developing detailed study plans and coordinating the efforts of multidisciplinary teams to ensure each phase is executed efficiently and on time. Site Management: Ensuring rigorous selection of clinical sites, training and supporting on-site teams, and monitoring compliance with protocols and regulations. Quality Oversight: Implementing quality control systems to guarantee data integrity and patient safety, while adhering to Good Clinical Practice (GCP) standards. Risk Management: Identifying potential risks, developing mitigation plans, and responding swiftly to challenges to minimize disruptions and deviations. Communication and Collaboration: Maintaining open and effective communication with stakeholders, including researchers, sponsors, regulators, and internal teams, to ensure synergy and transparency throughout the project. In Conclusion: Being a Clinical Operations Manager means being at the intersection of science, strategy, and management. Each day brings its challenges and opportunities, and it is with passion and determination that we work to advance clinical research. #ClinicalOperations #ClinicalTrials #Pharma #Innovation #Healthcare

I could not help it, I did a quick analysis 📊 on something that interests me.   According to data on LinkedIn job posts, currently the most sought-after #skills for those aspiring to venture into #projectmanager roles within the Healthcare sector in the UK, are: Project Management, Communication, Project Planning/Project Plans, Project Delivery, and Negotiation. If your focus is on opportunities within #pharmaceutical companies, the top three in-demand skills remain consistent: Project Management, Communication, and Project Planning/Project Plans. Additionally, expertise in Clinical Trials and Stakeholder Management enhances your profile in this sector. 🎯 #projecmanagement is a highly transferable skill, and understanding your audience's needs can significantly elevate the value you bring to the #team

Understanding project management nuances in clinical research is essential. Here's a quick guide to spotting differences in Project Manager profiles between CROs and pharma/biotech: 🔬 CROs: Juggling multiple projects, CRO Project Managers excel in client-facing roles and adaptability, managing diverse stakeholder expectations. 💼 Pharma/Biotech: Project Managers here focus on specific projects, aligning closely with organizational objectives. 🤝 Collaborative Dynamics: CROs emphasize client and vendor partnerships, while pharma/biotech values internal teamwork. 📈 Strategic Oversight: Pharma/biotech PMs align with broader goals, while in CROs the concentration is on client satisfaction. Recognizing these distinctions empowers tailored project management approaches. #clinicaltrials #clinicalstudies #projectmanagement #clinicalresearch #drugdevelopment

In healthcare & life sciences, project management is crucial for successful clinical research. As a Clinical Research and Regulatory Affairs Professional, I rely on strategic planning, effective communication, and meticulous attention to detail to manage projects. Agile methodologies help me optimize resources, streamline workflows, and proactively mitigate risks. One of my successful projects was implementing a Master Protocol Trial in oncology research. Coordinating with multiple stakeholders, designing a comprehensive protocol framework, and overseeing clinical trials across different phases were key to achieving timely recruitment and maintaining high data quality standards. My project management skills were also instrumental in driving efficient workflows for clinical sample management, collection, and analysis. By aligning projects with regulatory requirements and scientific objectives, I contribute to advancements in healthcare & life sciences. Let's connect and discuss how I can help drive your clinical research initiatives forward. #projectmanagement #clinicalresearch #healthcare #lifesciences

Throughout my career, I have gained valuable experience in the realm of clinical trials, particularly in the context of contract research organizations. With a strong background in leadership and a keen interest in advancing healthcare through well-executed trials, I have had the opportunity to contribute to various aspects of the clinical research landscape. One area of expertise I have developed is client management. Working closely with sponsors, I have successfully navigated the complexities of building strong relationships and meeting their expectations. I have honed my skills in understanding their unique needs, communicating effectively, and providing proactive support throughout the project lifecycle. Project oversight has been a critical component of my role. I have been entrusted with the responsibility of ensuring that trials are conducted efficiently and in compliance with regulations. From study initiation to close-out, I have guided multidisciplinary teams, fostered collaboration, and coordinated activities to ensure seamless execution of trials. Risk mitigation has always been at the forefront of my responsibilities. By assessing potential risks and implementing proactive strategies, I have successfully minimized the impact of unforeseen challenges on trial timelines and outcomes. This has involved developing comprehensive risk management plans and collaborating with cross-functional teams to ensure effective mitigation strategies are in place. Line management has been a part of my role, where I have overseen the performance and development of team members. With a focus on empowering and inspiring individuals, I have cultivated a culture of collaboration, accountability, and professional growth within my teams. Investigative site stewardship has been a significant aspect of my work. I have worked closely with research sites, nurturing relationships and providing ongoing support. By fostering effective communication and addressing site-specific needs, I have facilitated successful collaboration, resulting in efficient trial conduct and high-quality data collection. Lastly, my experience in strategic leadership has allowed me to contribute to the overall organizational vision and direction. By aligning clinical trial activities with larger business goals, I have facilitated decision-making processes and provided guidance on resource allocation and strategic initiatives. hashtag #ClinicalTrialsExpertise hashtag #ContractResearchOrganizations hashtag #ClientManagementExcellence hashtag #ProjectOversightSkills hashtag #PatientRecruitmentStrategies hashtag #MentoringLeadership hashtag #RiskMitigationSpecialist

🌟 Providing Vital Support to Biotech Companies in Europe 🌟 As a Biotech professional, I understand the critical need for skilled staff in Clinical Operations. 🌿 With the dynamic landscape of the industry, having the right team in place is essential for success. 🔬 At HRS, we specialise in meeting the contract staffing needs of Biotech companies across Europe. 💼 Our extensive network of experienced professionals can provide the expertise and support your organisation requires to thrive in this competitive sector. Whether you require clinical research associates, project managers, or other clinical operations specialists, we have the talent pool to cater to your unique requirements. 💡 With a focus on quality and efficiency, we aim to be your strategic partner in driving success and innovation. Let's collaborate to elevate your Clinical Operations to new heights! 💪 Interested in exploring how we can support your staffing needs? Drop a like or comment below to start the conversation. 🌍 #Biotech #ClinicalOperations #EuropeSuccess 🚀 #HRS #Science