Associate Director of Vendor Management

Who is BlueRock?BlueRock Therapeutics LP is an innovative clinical-stage biotechnology company specializing in cell therapy. Our mission is to develop groundbreaking medicines for individuals affected by neurological and ophthalmic disorders. Our lead investigational therapies, bemdaneprocel (BRT-DA01) for Parkinson’s disease and OpCT-001 for primary photore…

We are seeking a proactive and detail-oriented Data Management Vendor Manager Associate to join our dynamic team. In this role, you will be responsible for overseeing vendor relationships and ensuring seamless data management processes. Your contributions will be essential in fostering collaboration and optimizing performance across various projects.

We are seeking a detail-oriented Contracts Assistant specializing in Clinical Vendor Management to join our dynamic team. In this role, you will support the vendor management function by ensuring compliance with contractual obligations, assisting with contract negotiations, and maintaining accurate records for all vendor agreements. Your proficiency in contract management software and your keen eye for detail will be critical in this position.

Join Integrated Resources, Inc. as an Administrative Contracts Assistant specializing in Clinical Vendor Management. This pivotal role involves supporting our clinical operations team by managing contract processes, ensuring compliance, and facilitating communication between various stakeholders.

We are seeking an experienced and strategic Associate Director of Supply Chain Management to join our dynamic team at Korrobio. In this pivotal role, you will oversee the development and execution of supply chain strategies that align with our company objectives. You will lead initiatives to optimize processes, enhance efficiency, and drive cost savings across our supply chain operations.Your leadership will be crucial in fostering collaboration with internal teams and external partners to ensure seamless logistics, procurement, and inventory management. You will also play a key role in driving innovation and implementing best practices within the supply chain function.

Harvard University is seeking an innovative and strategic Associate Director of Research to lead groundbreaking research initiatives. The ideal candidate will possess a deep understanding of research methodologies, strong leadership skills, and a passion for academic excellence. This role involves collaborating with faculty and students to enhance research output and drive impactful scholarship.

We are seeking a dynamic and experienced Associate Director of Real Estate to join our growing team at Turner Townsend. In this pivotal role, you will lead and manage real estate projects, ensuring the delivery of high-quality outcomes while maintaining client satisfaction. You will work closely with clients to understand their needs, develop strategic plans, and oversee the execution of real estate initiatives. Your expertise in project management and real estate development will be crucial in driving project success.

Join Sobi as the Associate Director of European Supply Chain Management, where you will play a pivotal role in optimizing and managing our supply chain operations across Europe. You will lead a team of professionals, driving efficiency and ensuring that our products reach patients in a timely and effective manner. This is an exciting opportunity to contribute to the healthcare sector and make a meaningful impact.

Amylyx Pharmaceuticals is on a bold mission to revolutionize the treatment of diseases that have significant unmet needs. While others may see obstacles, we actively pursue opportunities with urgency, rigorous scientific methods, and a steadfast commitment to the communities we serve. As a clinical-stage company, we are currently targeting conditions such as post-bariatric hypoglycemia (PBH), Wolfram syndrome, and amyotrophic lateral sclerosis (ALS).Our mission is driven by our talented team, united by core values that include being audacious, curious, authentic, engaged, and accountable, fostering a culture of compassion. At Amylyx, we have assembled a highly experienced group dedicated to action, as the communities we serve cannot afford to wait. If you share our passion and are committed to addressing some of the most challenging problems in medicine, we invite you to explore this opportunity and apply.The OpportunityThe Clinical Data Management team at Amylyx Pharmaceuticals is in search of an Associate Director, Clinical Data Programmer. In this role, you will collaborate across functions to deliver hands-on data management support, programming expertise, and technical leadership. You will be responsible for developing, maintaining, and validating clinical databases, as well as executing computer programs to access, visualize, and report clinical trial data, adhering to clinical plans, ICH guidelines, and regulatory standards. As the Associate Director of Clinical Data Programming, proficiency in programming languages is essential for creating both textual and graphical representations that facilitate data cleaning and review.

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.

At Flagship Pioneering, we are pioneering advancements in biotechnology, creating innovative platform companies that aim to transform the world. We unite visionary scientific minds with entrepreneurial leaders and provide the necessary capital to boldly tackle humanity's most pressing health and sustainability challenges. Our work spans vital areas, including cancer detection and treatment, as well as nature-positive agriculture. What distinguishes Flagship is our unique ability to advance biotechnology by integrating life sciences innovation, company creation, and capital investment. This unprecedented approach unites our scientific founders, entrepreneurial leaders, and professional capital managers around a streamlined process that fosters innovation for the greater good of people and the planet. Our portfolio has made significant strides in addressing critical global issues: from rapidly vaccinating billions against COVID-19 to curing persistent diseases, enhancing health outcomes, preventing illness, and boosting agricultural resilience and sustainability. Flagship has been honored twice on FORTUNE’s “Change the World” list and recognized by Fast Company as one of the World’s Most Innovative Companies. Why Choose Flagship?At Flagship Pioneering, we offer inspiring leadership, a vibrant company culture, competitive compensation, comprehensive benefits, generous paid time off, a beautifully designed office stocked with unlimited snacks and daily free lunches, and meaningful work that promotes endless career growth.

Harvard University is hiring an Associate Director of Strategic Sourcing in IT to shape the university’s approach to acquiring technology resources. This position guides procurement strategy, leads sourcing projects, and works with IT teams to secure solutions that fit Harvard’s evolving needs. What you will do Direct strategic sourcing projects for IT products and services Negotiate contracts and oversee supplier partnerships Work with IT departments to understand their requirements and align procurement activities Promote efficiency and support innovation in technology sourcing Role impact This role contributes to Harvard’s mission by ensuring the university has access to dependable and effective technology. Decisions made in this position will influence operational efficiency and help foster ongoing innovation across campus.

The Opportunity:Relay Therapeutics is in search of an experienced and strategic regulatory leader to join our expanding regulatory team. In this pivotal role, you will define and implement groundbreaking regulatory strategies aimed at accelerating the development and approval of our innovative pipeline. As the global regulatory lead for relevant project teams, you will develop and execute comprehensive strategies for developmental programs. You will also be the primary liaison with the FDA, leading cross-functional teams to ensure successful domestic and international regulatory submissions, including IND, CTA, NDA, and MAA submissions.Your Role:Collaborate closely with regulatory, research, and development teams to design and implement innovative regulatory strategies for our dynamic programs, including both non-clinical and clinical regulatory strategies tailored to specific products.

Join Integrated Resources, Inc. as an Associate Director of Trial Master File Management, where you will play a pivotal role in overseeing the integrity and management of trial documents. You will be responsible for ensuring compliance with regulatory standards and optimizing document workflows to enhance trial efficiency.

Nuvalent seeks an Associate Director of Clinical Operations to join the team in Cambridge, MA or work remotely. This leadership role guides the execution of clinical trials, ensuring every step aligns with regulatory standards and internal protocols. The position partners with cross-functional teams to develop and deliver on clinical strategies, overseeing studies from planning through closeout. What you will do Direct clinical trial operations for multiple concurrent studies Maintain compliance with all regulatory requirements and company procedures Work closely with colleagues across departments to create and implement clinical strategies Supervise all aspects of study management, from initiation to completion Oversee budgets, timelines, and resource planning for clinical programs Mentor and guide junior staff within clinical operations Requirements Significant experience in clinical operations and project management Background working in pharmaceutical or biotechnology organizations Demonstrated ability to manage budgets and timelines Experience mentoring or managing team members

Harvard University is seeking a dynamic and strategic leader for the position of Associate Director of Development Administration. In this pivotal role, you will be responsible for overseeing various administrative functions within the Alumni Relations and Resource Development departments. You will work closely with senior management to implement effective strategies that enhance our fundraising initiatives and strengthen alumni engagement. Your expertise will be crucial in streamlining operations and ensuring that our development efforts are efficient and impactful.

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.

About BlueRock TherapeuticsBlueRock Therapeutics LP is at the forefront of cell therapy innovation, dedicated to developing groundbreaking treatments for neurological and ophthalmic disorders. Our clinical-stage investigational therapies, including bemdaneprocel (BRT-DA01) for Parkinson’s disease and OpCT-001 for primary photoreceptor diseases, represent a significant leap in medical science. Founded in 2016 through a partnership between Versant Ventures and Leaps by Bayer, we are driven by a culture of resilience, urgency for transformation, integrity, and a deep commitment to community.Our VisionWe specialize in harnessing the potential of universal pluripotent stem cells, guiding their differentiation into functional cells for allogeneic cellular therapies aimed at a wide range of conditions. Our passion lies in advancing cellular and gene therapy, ultimately improving the lives of millions of patients by delivering innovative treatment options.We are on the lookout for dynamic individuals who thrive in a collaborative and vibrant environment, and who are dedicated to pioneering cellular therapies that can transform patient outcomes.As we continue to make strides in cellular therapies, we are inviting an exceptional professional to join our Clinical Development team, playing a crucial role in overseeing preclinical, translational IND-enabling, and clinical development activities for our neurology programs.The Associate Medical Director of Neurology will lead scientific and medical initiatives for our neurology programs. Reporting directly to the Vice President of Clinical Development, this individual will collaborate closely with program leads and subject matter experts to enhance our development pipeline. The ideal candidate will serve as a clinical and scientific authority, fostering both internal and external partnerships to drive program success.

Amylyx Pharmaceuticals is dedicated to pioneering innovative treatments for diseases with significant unmet needs. We view challenges as opportunities, driving our mission with urgency, robust scientific inquiry, and a steadfast commitment to the communities we serve. As a clinical-stage company, we focus on addressing conditions such as post-bariatric hypoglycemia (PBH), Wolfram syndrome, and amyotrophic lateral sclerosis (ALS).Our mission is powered by our talented team, guided by core values of audacity, curiosity, authenticity, engagement, and accountability—fostering a culture of care. We are assembling an experienced group of individuals ready to take meaningful action, as the communities we support cannot afford to wait. If you share this passion and are committed to addressing some of the toughest challenges in medicine, we invite you to explore this exciting opportunity and apply.The OpportunityThe Associate Director of Healthcare Professional Marketing will play a pivotal role within our Marketing team, spearheading the healthcare professional (HCP) engagement strategy for the launch of avexitide aimed at treating post-bariatric hypoglycemia (PBH). This position will concentrate on identifying, understanding, and engaging key segments of HCPs, including thought leaders and early adopters, to enhance awareness of PBH and the therapeutic role of avexitide. This individual will collaborate closely with our sales force and field-facing teams, including Thought Leader Liaisons (TLLs), to ensure aligned, educational, and impactful engagement with the HCP community. Through the development of tailored promotional strategies and educational initiatives, you will enhance the HCP's comprehension of PBH, promote informed clinical discussions, and facilitate successful product adoption at launch.This is a remarkable opportunity for a strategic, collaborative, and results-driven HCP marketer to establish a high-impact engagement platform in a complex and underserved therapeutic landscape.

As an Associate Medical Director specializing in Drug Safety and Pharmacovigilance at Nuvalent, you will play a pivotal role in ensuring the safety and efficacy of our pharmaceutical products. You will be responsible for leading safety assessments, developing risk management strategies, and overseeing the pharmacovigilance processes to comply with regulatory requirements. Your expertise will contribute to the overall mission of improving patient outcomes through innovative therapies.