Bench Scientist

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.

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.

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.

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.

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 our innovative team as a Senior Scientist where you'll drive critical research projects and make a significant impact in the field. We are seeking a highly motivated individual with a passion for scientific discovery and a strong background in relevant disciplines.

We are seeking a motivated and detail-oriented Bench Scientist to join our dynamic team in Cambridge. This entry-level position is an excellent opportunity for recent graduates or those new to the field of scientific research. As a Bench Scientist, you will play a crucial role in conducting experiments, analyzing data, and contributing to innovative projects. If you are passionate about science and eager to learn, we encourage you to apply!

Join Artech Information Systems LLC as a Scientist in Cambridge, where you will contribute to groundbreaking research and innovative solutions in a collaborative environment. Your expertise will help drive scientific advancements and enhance our projects.

AbbVie is seeking a talented and motivated Associate Scientist II or Scientist I to join our dynamic In Vivo Pharmacology team in Cambridge. As part of our innovative research environment, you will play a crucial role in advancing our understanding of pharmacological mechanisms through in vivo studies. This position offers an exciting opportunity to contribute to groundbreaking research that has the potential to transform patient care.

As an Associate Scientist III, you will play a crucial role in advancing our scientific research initiatives. You will collaborate with cross-functional teams to design, execute, and analyze experiments that contribute to our innovative projects. Your expertise will help drive our mission forward, ensuring that we continue to push the boundaries of scientific discovery.

Join our dynamic team at Integrated Resources Inc. as an Associate Scientist II, where you will play a crucial role in advancing our innovative projects. In this position, you will engage in various scientific experiments and analyses, contributing to the development of cutting-edge solutions.

We are seeking a motivated and detail-oriented Bench Scientist to join our dynamic team in Cambridge. In this role, you will be responsible for conducting experiments, analyzing results, and contributing to various research projects. This is an excellent opportunity for a recent graduate or entry-level professional to gain valuable experience in a laboratory setting.

Join Integrated Resources Inc. as an Associate Scientist I, where you will contribute to innovative scientific research and development projects. As a pivotal part of our team, your role will involve conducting experiments, analyzing data, and collaborating with multidisciplinary teams to advance our scientific objectives.

We are seeking a highly motivated and detail-oriented Associate Scientist I to join our dynamic team in Cambridge. The ideal candidate will assist in the design and execution of experiments, analysis of data, and contribute to various projects within our research initiatives.

Join Integrated Resources Inc. as an Associate Scientist where you will engage in groundbreaking research and contribute to innovative projects. This role offers an exciting opportunity to work in a collaborative environment, driving advancements in our scientific endeavors.

We are seeking a highly motivated and detail-oriented Research Scientist to join our innovative team in Cambridge. In this role, you will conduct groundbreaking research, analyze data, and contribute to the development of new solutions in our field. You will work collaboratively with cross-functional teams to drive projects from ideation to execution, ensuring scientific rigor and excellence.

Your Contribution at Lila At Lila, we are assembling a dynamic and empowered AI safety team dedicated to proactively addressing the potential risks associated with scientific superintelligence. This team will collaborate closely with all core departments, including science, model training, and lab integration, to craft a customized safety strategy that aligns with our unique objectives and deployment methods. Key responsibilities will encompass the development of technical safety strategies, engagement with the broader ecosystem, and the creation of essential technical documentation, including risk assessments and capability evaluations. Your Key Responsibilities Design and execute evaluations to identify scientific risks—focusing on both established and emerging threats—from state-of-the-art scientific models integrated with automated physical laboratories. Develop initial proof-of-concept safety measures, such as machine learning models designed to detect and mitigate unsafe behaviors from scientific AI models and physical laboratory outputs. Gain a comprehensive understanding of various model capabilities, primarily within scientific contexts but also extending to non-scientific domains (e.g., persuasion, deception) to shape Lila's overarching safety strategy. Engage in high-quality research initiatives as needed to evaluate and restrict scientific capabilities effectively. Qualifications for Success A Bachelor's degree in a relevant technical field (e.g., computer science, engineering, machine learning, mathematics, physics, statistics) or equivalent experience. Proficient programming skills in Python and hands-on experience with machine learning frameworks (such as Inspect) for large-scale evaluations and structured testing. Demonstrated experience in constructing evaluations or conducting red-teaming exercises pertaining to CBRN/cyber risks or frontier model capabilities, encompassing both unsafe and benign attributes. Background in designing and/or implementing AI safety frameworks in cutting-edge AI enterprises. Exceptional ability to communicate intricate technical concepts and issues to audiences without technical expertise. Desirable Qualifications A Master’s or PhD in a field pertinent to safety evaluations of AI models within scientific areas or another technical discipline. Publications in AI safety, evaluations, or model behavior at leading ML/AI conferences (such as NeurIPS, ICML, ICLR, ACL) or model release documentation. Experience exploring risks arising from novel scientific advancements (e.g., biosecurity, computational biology) or utilizing specialized scientific tools (e.g., large-scale foundational models in science).

AbbVie Inc. is seeking an Associate Scientist II with a focus on In Vivo Pharmacology to join the team in Cambridge. This position supports research that aims to improve patient outcomes through new drug discovery. Role overview The Associate Scientist II will perform in vivo experiments and handle data analysis as part of ongoing research projects. Collaboration with colleagues from different scientific backgrounds is a key part of this role. Key responsibilities Conduct in vivo pharmacology experiments as part of drug discovery initiatives Analyze and interpret experimental data to support research goals Work closely with cross-functional teams to drive projects forward Location This position is based in Cambridge.