Associate/Senior Associate at Flagship Pioneering | Cambridge, MA

Join Integrated Resources Inc. as a Senior Associate in Pharmacovigilance, where you will play a crucial role in ensuring drug safety and regulatory compliance. We are seeking a detail-oriented professional who is passionate about pharmacovigilance and eager to make a significant impact in the pharmaceutical industry.

Join our dynamic team at Integrated Resources, Inc. as an Associate Director of Pharmacovigilance. In this pivotal role, you will oversee the safety and efficacy of pharmaceutical products, ensuring compliance with regulatory standards and advancing our commitment to patient safety.Your expertise in pharmacovigilance will guide our strategic initiatives, collaborating with cross-functional teams to enhance product safety and regulatory submission processes.

We are seeking a highly skilled Associate Director of Drug Safety and Pharmacovigilance to join our dynamic team at Nuvalent. This pivotal role involves overseeing drug safety operations, ensuring compliance with regulatory requirements, and enhancing the pharmacovigilance strategy. The ideal candidate will possess a deep understanding of drug safety processes and a passion for advancing patient safety in the pharmaceutical industry.

Join Integrated Resources, Inc. as a Pharmacovigilance Scientist and contribute to the safety and efficacy of pharmaceutical products. In this role, you will be responsible for monitoring, assessing, and reporting adverse effects associated with drug therapies. Your expertise will directly impact patient safety and regulatory compliance while collaborating with cross-functional teams.

Scholar Rock, Inc. is a pioneering biopharmaceutical firm dedicated to the discovery, development, and delivery of transformative therapies for individuals suffering from serious diseases with significant unmet medical needs. As a recognized leader in the biology of the transforming growth factor beta (TGFβ) superfamily of proteins, Scholar Rock is committed to advancing innovative treatments where the modulation of protein growth factors is crucial. Over the last decade, we have developed a robust pipeline aimed at redefining the standard of care for neuromuscular conditions, cardiometabolic disorders, cancer, and other diseases where growth factor-targeted therapies can radically change patient outcomes. Scholar Rock is the first and only company to demonstrate clinical proof of concept for a muscle-targeted treatment in spinal muscular atrophy (SMA). Our commitment to unlocking unique therapeutic strategies is driven by our proprietary platform, which has generated novel monoclonal antibodies designed to modulate protein growth factors with remarkable precision. By leveraging cutting-edge scientific advancements in therapeutic areas that have historically been overlooked by conventional treatments, Scholar Rock tirelessly works to create new avenues for patient care. Discover more about our innovative approach at ScholarRock.com and follow us on @ScholarRock and LinkedIn.Position Overview:The Senior Medical Director of Drug Safety & Pharmacovigilance plays a critical role within the company, significantly influencing the development and lifecycle management of drug projects. This position is responsible for defining and implementing safety strategies and providing expert guidance during both pre- and post-approval phases for assigned products. The Senior Medical Director will proactively lead risk management initiatives in compliance with global regulatory standards, continuously evaluating safety data, conducting signal detection, and managing the safety profiles of compounds. Additionally, this role will involve close collaboration with cross-functional teams to achieve project objectives within established timelines and quality standards.

Join Integrated Resources Inc. as a Senior Drug Safety Associate and contribute to the vital field of drug safety and pharmacovigilance. In this role, you will play a key part in monitoring and ensuring the safety of pharmaceutical products, working closely with cross-functional teams to assess risk and implement safety measures.

As a Pharmacovigilance Coordinator at Integrated Resources, Inc., you will play a critical role in ensuring the safety and efficacy of pharmaceutical products. You will be responsible for the monitoring, assessment, and reporting of adverse drug reactions, working closely with healthcare professionals and regulatory bodies.This position requires strong analytical skills, attention to detail, and a commitment to maintaining the highest standards of patient safety.

AbbVie is seeking a highly skilled Associate Director to lead our Safety Operations Portfolio. This pivotal role involves overseeing safety operations while ensuring compliance with regulatory requirements. The ideal candidate will possess exceptional leadership skills and a strong background in pharmacovigilance.Join our dynamic team and contribute to advancing healthcare solutions that enhance patient safety and improve health outcomes. This is an exciting opportunity for professionals looking to make a meaningful impact in the pharmaceutical industry.

As a Drug Safety Associate at Integrated Resources Inc., you will play a crucial role in ensuring the safety and efficacy of pharmaceutical products. You will be responsible for monitoring and evaluating adverse events, coordinating safety reports, and contributing to the overall pharmacovigilance efforts within our organization. Your attention to detail and analytical skills will be vital in supporting our commitment to patient safety.

Join BioMed Realty as a Senior Associate in Leasing, where you'll be at the forefront of driving our property leasing efforts. In this pivotal role, you will engage with clients, negotiate lease agreements, and ensure that our leasing strategies align with company goals. Your expertise will be essential in fostering relationships with key stakeholders and contributing to our growth in the life sciences real estate sector.

We are seeking a highly motivated Senior Research Associate to join our dynamic team at Integrated Resources, Inc. In this pivotal role, you will conduct advanced research, analyze data, and contribute to innovative projects that drive our mission forward. If you are passionate about scientific research and eager to make an impact, we want to hear from you!

We are seeking a talented and dedicated Senior Research Associate to join our dynamic team in Cambridge. In this role, you will contribute to innovative research projects and collaborate with interdisciplinary teams to drive impactful findings.

Join our dynamic team at Integrated Resources Inc. as a Senior Operations Associate. In this pivotal role, you will be responsible for optimizing operational processes and enhancing productivity. Collaborate with cross-functional teams to drive continuous improvement initiatives and deliver exceptional results. Your analytical mindset and problem-solving skills will be crucial in identifying opportunities for operational efficiencies.

Your Contribution at Lila Sciences Lila Sciences is actively seeking a dedicated (Senior) Research Associate to become an integral part of our dynamic Life Sciences team. This pivotal role will be centered around the formulation of lipid nanoparticles (LNPs), their functionalization with targeting ligands, and the characterization of the resulting targeted LNPs (tLNPs). The ideal candidate will possess substantial hands-on experience in LNP formulation and characterization, bioconjugation, protein characterization, and automation technologies. Your expertise will significantly enhance our understanding of the delivery space, enabling a high-throughput closed-loop screening cascade for tLNPs. You will work collaboratively with professionals across protein, cell biology, automation, chemistry, machine learning, and data science teams to establish advanced tools for targeted nucleic acid delivery. Your Key Responsibilities Design, execute, and characterize LNP formulations utilizing various scales and mixing modalities (e.g., DLS, ribogreen, TNS). Develop and optimize high-throughput ligand conjugation and purification methodologies, leveraging automation and robotics to maximize throughput. Collaborate with cell assay and antibody experts to screen candidates across diverse tissue targets in in vivo models. Engage with chemists, biologists, engineers, and data scientists to document processes, share insights, and refine best practices in autonomous flow chemistry. Create, implement, and uphold Standard Operating Procedures (SOPs) for both existing and emerging lab processes. Your Qualifications for Success MSc in Chemical Engineering, Biomedical Engineering, Pharmaceutical Sciences, or a closely related field with 3+ years of hands-on experience in targeted LNP production or a BSc with 5+ years of relevant experience. Industry experience is highly desirable. Strong proficiency in bioanalytical techniques (e.g., DLS, fluorescence spectroscopy, electrophoresis, in vitro assays). Experience in protein and antibody design and characterization. Familiarity with automation and high-throughput workflows is preferred. Exceptional troubleshooting, communication, and collaboration skills, with a proven ability to work effectively across interdisciplinary teams. About Lila Sciences Lila Sciences is at the forefront of innovation as the world's first scientific superintelligence platform and autonomous laboratory focused on life sciences, chemistry, and materials science. We are pioneering a new era of limitless discovery by harnessing AI capabilities to enhance every facet of the scientific method. Our mission is to leverage scientific superintelligence to address humanity's most pressing challenges.

Join our dynamic team at Integrated Resources, Inc. as a Senior Associate. This role offers an exciting opportunity to contribute to impactful projects and collaborate with talented professionals. As a Senior Associate, you will leverage your expertise to drive our initiatives forward, ensuring excellence in all aspects of our work.

Join Integrated Resources, Inc. as a Senior Associate in Controlled Document Management. In this pivotal role, you will oversee the management of critical documents to ensure compliance and operational excellence. Your expertise will contribute significantly to our projects, delivering high-quality results while maintaining stringent regulatory standards.

Join Lila Sciences as a Senior Research Associate or Associate Scientist in the Protein Science department, focusing on our cutting-edge Antibody Platform. You will play a crucial role in advancing our research initiatives, contributing to the development of innovative antibody-based therapeutics. This position offers the opportunity to collaborate with a talented team dedicated to scientific excellence and the pursuit of transformative solutions in healthcare.

Your Impact at Lila Sciences Join our innovative high-throughput autonomous chemistry team as a Senior Research Associate / Associate Scientist. This hands-on position bridges the fields of organic and inorganic synthesis, advanced characterization, and laboratory automation. You will design and implement high-throughput experiments, synthesize small molecules, and conduct thorough downstream analysis alongside senior scientists. Your efforts will contribute to translating ambitious product objectives into scalable experimental workflows that significantly influence our company's growth. This role provides a unique opportunity to engage with automated chemistry platforms, giving you real ownership of experiments that shape our scientific strategy and direction. Ideal candidates are execution-oriented, excel in dynamic laboratory settings, and are passionate about developing deep technical skills while making impactful contributions to the future of chemical discovery at Lila Sciences. What You’ll Be Building Independently conduct experiments for the synthesis, purification, and characterization of organic and inorganic small molecules. Optimize reactions, develop methodologies, and analyze analytical data to inform project decisions. Convert initial concepts into reliable, functional experiments. Utilize retrosynthetic analysis to assist in the synthesis of target molecules. Operate Schlenk lines, gloveboxes, and various inert-atmosphere systems for sensitive materials. Employ PAT tools (UPLC, LCMS, NMR, IR, Fluorescence, DLS) to monitor reactions, ensure quality control, and produce high-quality data for machine learning workflows. Leverage automation and AI-driven technologies to streamline workflows and reduce experimental turnaround times. Collaborate with engineers, ML scientists, and stakeholders to validate model-recommended conditions, analyze trends, troubleshoot challenges, and clearly communicate results through reports, discussions, and presentations. Maintain meticulous documentation of results, ensuring accurate digital records while adhering to EHS and laboratory best practices. What You’ll Need to Succeed M.S. in Chemistry or a related field (such as organic, organometallics, or catalysis) with a minimum of 2 years of relevant laboratory experience, or a B.S. with 5 years of experience. Hands-on experience in organic and inorganic synthesis, purification processes, chromatographic techniques, and product analysis. Strong grasp of retrosynthesis, reaction mechanisms, and method optimization workflows. Proficiency in utilizing laboratory automation tools and systems. Excellent problem-solving skills and the ability to work collaboratively in a team-oriented environment.

About UsAt Stone King, we are a forward-thinking and purpose-driven law firm dedicated to serving the Business & Social Enterprise, Charity, Education, Faith, and Private Client sectors. Our collaborative culture and core values are deeply rooted in our commitment to doing right by our clients, our communities, and our team members. This dedication, alongside our passion for the sectors we engage with, has positioned Stone King as a national leader in our areas of expertise.The OpportunityWe are excited to invite applications for the role of Senior Associate Solicitor within our dynamic and ambitious Construction team. This position offers the flexibility of being based at any of our offices, complemented by hybrid working arrangements. Occasional travel to other offices or client sites may be required depending on project demands.Joining our team means the opportunity to advance your career in a highly respected national firm. You will have the chance to work with a distinguished client base and closely collaborate with our nationally acclaimed Education team, consistently recognized as Tier 1 by clients and holding individual accolades in both Chambers and Legal 500.In addition to your work in the Education sector, you will also engage in a variety of non-contentious construction matters across other sectors, particularly within the Charity and Business communities.Reasons to ApplyBe a Key Player: Become an integral part of a team during an exciting period of growth.Collaborative Environment: Join an ambitious, friendly, and national firm where our culture and values are central to our operations. We believe our people are our greatest asset and continuously strive to create the best workplace.Comprehensive Benefits: Enjoy excellent benefits focused on well-being and professional development.Flexible Working: We are proud signatories of the Mindful Business Charter, demonstrating our commitment to mental health and well-being. We are eager to support our team members in achieving a healthy work/life balance and are open to discussing flexible working arrangements with prospective candidates.Key ResponsibilitiesYour general duties will include, but are not limited to:Efficiently manage your own caseload, while delegating tasks and providing supervision to junior team members as necessary.Build and nurture relationships with both existing and prospective clients, ensuring exceptional service delivery.Foster a collaborative and collegial work environment within your immediate team and the broader firm.Communicate effectively and promptly with both colleagues and clients.Engage in continuous professional development, staying informed about legal trends and changes in the field.Deliver high-quality work for colleagues and clients alike, adhering to the highest professional standards.