LumaBridge

?? We’re Hiring! Clinical Research Associate (CRA), Senior CRA, and Contract CRA (3-6 months) ?? Are you passionate about advancing oncology clinical trials and ready for your next impactful opportunity in cancer research? LumaBridge is on a mission to bring life-changing therapies to patients faster, and we’re looking to expand our incredible team with CRAs, Senior CRAs, and a Contract CRA (3-6 months)! What We’re Looking For: ?? Experience monitoring oncology clinical trials (5+ years for Sr. CRA roles). ?? Strong background with CRO experience and site monitoring. ?? Proven ability to drive clinical studies forward with precision and excellence. ?? A collaborative, detail-oriented, and mission-driven mindset. Why LumaBridge? ?? We’re a team of passionate professionals dedicated to improving lives. ?? You’ll work in a supportive and innovative environment. ?? We’re committed to empowering our employees to grow their careers while making a real impact. If you’re ready to take the next step in your career and help lead the charge in advancing oncology research, we’d love for you to explore opportunities below on our careers page. Together, we can make a difference. ?? #ClinicalResearch #Oncology #CRA #SrCRA #WeAreLumaBridge #JoinOurTeam

LumaBridge is looking to bring on a Clinical Research Associate or Sr. Clinical Research Associate to help support our Phase I-III, Oncology-focused clinical trials. Please reach out if you are interested in joining this growing team! #LumaBridge #CRA

At LumaBridge, we navigate compliance for the biotech's that we support. One key aspect is the?Development Safety Update Report (DSUR), which has become a cornerstone for annual regulatory submissions. ???What is DSUR? The DSUR is a comprehensive annual report that provides a detailed overview of the safety profile of investigational drugs. It aligns with the guidelines set by the International Council for Harmonisation (ICH) and is designed to harmonize the reporting process across different regions. ???Why DSUR Matters: Enhanced Safety Monitoring:?DSURs offer a thorough evaluation of safety data collected during the reporting period, ensuring that any potential risks are identified and addressed promptly. Regulatory Compliance:?By adhering to DSUR guidelines, companies can meet the regulatory requirements of both the FDA, EU, and Japan streamlining the submission process. Global Harmonization:?The DSUR format promotes consistency and transparency in safety reporting, facilitating better communication between regulatory authorities and sponsors. ???Key Components of a DSUR: Executive Summary:?A concise overview of the report's findings. Cumulative Safety Data:?Detailed analysis of adverse events and safety signals. Clinical Trial Information:?Updates on ongoing and completed studies. Risk Benefit:?Strategies to mitigate identified risks. At LumaBridge we can leverage the DSUR framework, to assist in ensuring that our investigational drugs are developed with the highest standards of safety and efficacy. Let's continue to prioritize patient safety and regulatory excellence in our journey towards innovative clinical trial solutions. We?are ready and available?to support?your needs. Get in touch?by clicking the link here >?LumaBridge #RegulatoryAffairs #Pharma #DrugDevelopment #DSUR #Compliance #PatientSafety #biotech #oncology #cancer?#concepttoclinic

Today, February 4th, is World Cancer Day—a day of unity, awareness, and action. ?? ? At LumaBridge, we stand alongside patients, caregivers, and researchers in the fight against cancer. This disease has touched so many lives, challenging us with its hardships but also inspiring unwavering resilience and hope. ? We honor the strength of those who have faced cancer—those who continue to fight, those we have lost, and the loved ones who support them. Their stories fuel our commitment to advancing cancer research and providing access to innovative treatments. ? Today is a reminder that early detection, education, and groundbreaking research are key in the fight against cancer. Together, we can make a difference—through awareness, advocacy, and supporting scientific progress that brings us closer to a world without cancer. ? Let’s take this moment to spread compassion, offer support, and stand together in hope. ? #WorldCancerDay #TogetherWeCan #LumaBridge #Oncology #ClinicalResearch

?? We're Hiring: Quality Assurance Manager! ?? Key Responsibilities: ? Oversee audits, CAPAs, and inspection readiness. ? Develop and validate eQMS. ? Drive continuous improvement and compliance. What We Need: ? 7+ years QA experience (4+ in clinical research). ? Strong knowledge of FDA and ICH guidelines. ? Experience with eQMS platforms and vendor audits. ?? Apply below and join us in advancing clinical research excellence at LumaBridge! #Hiring #QualityAssurance #ClinicalResearch #LumaBridge #RemoteJob

?? We’re Hiring! Clinical Research Associate (CRA), Senior CRA, and Contract CRA (3-6 months) ?? Are you passionate about advancing oncology clinical trials and ready for your next impactful opportunity in cancer research? LumaBridge is on a mission to bring life-changing therapies to patients faster, and we’re looking to expand our incredible team with CRAs, Senior CRAs, and a Contract CRA (3-6 months)! What We’re Looking For: ?? Experience monitoring oncology clinical trials (5+ years for Sr. CRA roles). ?? Strong background with CRO experience and site monitoring. ?? Proven ability to drive clinical studies forward with precision and excellence. ?? A collaborative, detail-oriented, and mission-driven mindset. Why LumaBridge? ?? We’re a team of passionate professionals dedicated to improving lives. ?? You’ll work in a supportive and innovative environment. ?? We’re committed to empowering our employees to grow their careers while making a real impact. If you’re ready to take the next step in your career and help lead the charge in advancing oncology research, we’d love for you to explore opportunities below on our careers page. Together, we can make a difference. ?? #ClinicalResearch #Oncology #CRA #SrCRA #WeAreLumaBridge #JoinOurTeam

?? We're Hiring: Quality Assurance Manager! ?? Key Responsibilities: ? Oversee audits, CAPAs, and inspection readiness. ? Develop and validate eQMS. ? Drive continuous improvement and compliance. What We Need: ? 7+ years QA experience (4+ in clinical research). ? Strong knowledge of FDA and ICH guidelines. ? Experience with eQMS platforms and vendor audits. ?? Apply below and join us in advancing clinical research excellence at LumaBridge! #Hiring #QualityAssurance #ClinicalResearch #LumaBridge #RemoteJob

?? We're Hiring: Quality Assurance Manager! ?? Key Responsibilities: ? Oversee audits, CAPAs, and inspection readiness. ? Develop and validate eQMS. ? Drive continuous improvement and compliance. What We Need: ? 7+ years QA experience (4+ in clinical research). ? Strong knowledge of FDA and ICH guidelines. ? Experience with eQMS platforms and vendor audits. ?? Apply below and join us in advancing clinical research excellence at LumaBridge! #Hiring #QualityAssurance #ClinicalResearch #LumaBridge #RemoteJob

January is Cervical Cancer Awareness Month, and at LumaBridge, we want to raise awareness, promote prevention, and support those impacted by this disease. ? Cervical cancer is one of the most preventable cancers, yet it still affects thousands of women every year. Early detection through regular screenings, such as pap smears and HPV tests, is key to reducing the risk. ? Let’s join together to: ?? Encourage loved ones to schedule routine screenings. ??Educate on the importance of the HPV vaccine for prevention. ??Support ongoing research and awareness efforts to fight cervical cancer. ? Together, we can make a difference. Share this post to spread awareness and empower others! ?? ? #CervicalCancerAwarenessMonth #PreventionIsKey #WomensHealth #LumaBridgeCares

We like to celebrate when good things happen to our employees, especially when it is done by their own hard work. We at LumaBridge wanted to take a moment to celebrate one of our standout team members obtaining her Certification in Clinical Data Management (CCDM). This program is tailored to identify credible, trained and qualified CDM professionals. The CCDM certification is globally recognized credential for CDM professionals, demonstrating proficiency in core CDM competencies, including data collection, validation analysis, and regulatory compliance. We are extremely proud of Samantha Garritano, MS and all the hard work she's performed here at LumaBridge #oncology #CRO #cancer #clinicalresearch #innovator #womaninstem #biotech #clinicaldatamanagement