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Associate Director, Pharmacovigilance Scientist

Deciphera Pharmaceuticals, Inc.

Full-time|On-site|Waltham

As the Associate Director of Pharmacovigilance, you will play a crucial role in ensuring the safety and efficacy of our pharmaceutical products. You will lead a team dedicated to monitoring and evaluating adverse drug reactions, while also collaborating closely with regulatory bodies to uphold our commitment to patient safety. Your expertise will contribute …

Apr 6, 2026

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Medical Director of Pharmacovigilance

Deciphera Pharmaceuticals, Inc.

Full-time|On-site|Waltham

Join Deciphera Pharmaceuticals as a Medical Director of Pharmacovigilance, where you will play a pivotal role in ensuring the safety of our products. Reporting directly to the Senior Medical Director, this position is based in our Waltham office and is integral to our commitment to patient safety.As a Medical Director, you will oversee global pharmacovigilance activities for both marketed and investigational products. Your responsibilities will include the comprehensive review and analysis of safety data, identification of safety signals, and management of the benefit-risk profile for assigned compounds. You will keep senior management informed about safety issues and may represent Deciphera at various internal and external meetings.The ideal candidate will thrive in an entrepreneurial environment and demonstrate the flexibility to contribute to the safety understanding of our compounds throughout their lifecycle. You will engage with multiple levels of management and play a critical role in advancing our pharmacovigilance initiatives.Key Responsibilities:Lead ongoing safety surveillance, benefit-risk assessments, and risk management for assigned products.Provide pharmacovigilance expertise to support decision-making based on risk/benefit evaluations and data analysis.Conduct medical reviews of adverse event reports for both marketed and investigational products, ensuring adherence to procedures and timelines.Ensure consistent and high-quality medical interpretation in adverse event case assessments.Support cross-functional teams with protocol-related medical guidance, including safety topics and patient eligibility considerations.Contribute to the development of protocols, Investigative Drug Brochures, Informed Consent Forms, and Case Report Forms.Review trial-related adverse events and ensure consistency in assessment.Participate in team meetings and vendor discussions as necessary.Support audits and inspections as a subject matter expert for assigned programs.Provide training to team members and vendors regarding product safety and medical review processes.Complete tasks in a timely manner, notifying relevant parties of any necessary changes.Engage in scientific literature review for periodic safety reports and signal detection.

Mar 13, 2026

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Associate Research Scientist at mindlance2 | Waltham

mindlance2

Full-time|On-site|Waltham

We are seeking a passionate and detail-oriented Associate Research Scientist to join our innovative team at mindlance2. In this role, you will contribute to groundbreaking research initiatives, collaborating with a team of experts to drive scientific discovery.

Jun 22, 2016

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Associate Director/Director of Analytical & GMP Quality Assurance Operations

Crescent Biopharma

Full-time|On-site|Waltham, MA

At Crescent Biopharma, we aspire to transform the landscape of oncology by developing cutting-edge therapies tailored for cancer patients. Our innovative pipeline includes a leading PD-1 x VEGF bispecific antibody, alongside state-of-the-art antibody-drug conjugates. By harnessing diverse therapeutic modalities and established targets, we aim to expedite the development of potentially groundbreaking treatments, whether as standalone interventions or in combination therapies targeting various solid tumors. For more insights into our mission and vision, visit our website and connect with us on LinkedIn and X.We are currently in search of an Associate Director or Director of Analytical & GMP Quality Assurance Operations. In this pivotal role, you will oversee and guide the QA functions related to analytical development, quality control operations, and GMP quality activities across our clinical-stage biologics and ADC programs. Collaboration with cross-functional teams, including CMC, Analytical Sciences, Quality Control, and Technical Operations, as well as external manufacturing and testing partners, will be key to ensuring compliance with phase-appropriate GMP standards, maintaining data integrity, and ensuring inspection readiness within a dynamic outsourced operational framework. Your strategic vision will be instrumental in shaping Crescent's analytical quality strategy and driving the disciplined execution of core quality systems that align with our aggressive development timelines.

Mar 10, 2026

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Associate Director of Access Strategy

Sobi

Full-time|On-site|Waltham

As the Associate Director of Access Strategy at Sobi, you will play a pivotal role in shaping the strategies that enhance patient access to our innovative therapies. This position requires a strategic thinker who is passionate about improving healthcare accessibility and is adept at navigating the complexities of the healthcare landscape. You will work closely with cross-functional teams to develop and implement access strategies that align with our organizational goals and promote patient-centric outcomes.

Apr 30, 2026

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Pharmacology Scientist/Senior Scientist

Biocytogen Boston Corp

Full-time|On-site|Waltham, Massachusetts, United States

Biocytogen Boston Corp is on the lookout for a dynamic and skilled Pharmacology Scientist or Senior Scientist to enhance our preclinical research capabilities in both in vivo and in vitro settings. Our focus spans across immunology, immuno-oncology, metabolic diseases, and neurology. This position is perfect for individuals with extensive knowledge in pharmacological studies, disease model development, and cell-based assays who are excited about assessing innovative therapeutic agents for our clients.The right candidate will play a vital role in our growing CRO team, engaging in experimental work as well as strategic project management to support our biotech and pharmaceutical collaborators.Key ResponsibilitiesIn Vivo PharmacologyDesign and create animal models, conducting in vivo experiments to assess the biological effectiveness of new therapeutic compounds.Lead in vivo service projects and preclinical studies, serving as Project Manager or Study Director.Conduct animal handling, tumor inoculation, drug administration via various routes, blood and tissue collection, tumor measurements, and PK/PD studies.Develop and execute internal model-building projects while characterizing diverse humanized mouse models.Provide troubleshooting support and technical mentorship to junior team members.Work closely with the BD/Sales team to strategize client project planning and technical discussions.Deliver presentations of project outcomes to clients and internal stakeholders; draft comprehensive scientific reports and summaries.Guide and support the development of junior research associates.In Vitro and Ex Vivo PharmacologyIndependently establish, validate, and execute a wide variety of in vitro and ex vivo assays, which include:Immune cell profiling from blood and tissues.Functional assays utilizing primary cells (T cells, NK cells, macrophages).Cytokine profiling, cytotoxicity, and apoptosis assays.Innovate new assay technologies by reviewing scientific literature and adapting methodologies from partnerships and internal collaborations.Perform flow cytometry (FACS), ELISA, Western blot, qRT-PCR, and multiplex cytokine analyses.Contribute to the design and execution of in vivo pharmacology studies from an in vitro perspective.Present research results in internal meetings and contribute to external scientific discussions.

Dec 22, 2025

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Associate Director, Regulatory Affairs CMC

AbbVie Inc.

Full-time|On-site|Waltham

Join AbbVie as an Associate Director in Regulatory Affairs with a focus on Chemistry, Manufacturing, and Controls (CMC). In this pivotal role, you will lead cross-functional teams to ensure compliance with regulatory requirements while advancing our innovative therapies. As a leader, you will drive the development of CMC submission strategies, collaborate with internal and external stakeholders, and support the overall regulatory strategy for our product pipeline.

Apr 30, 2026

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Associate Director of Sales Operations

Deciphera Pharmaceuticals, Inc.

Full-time|On-site|Waltham

Deciphera Pharmaceuticals, Inc. is on the lookout for a seasoned Associate Director of Sales Operations to spearhead and enhance our field-facing operational strategies. This pivotal role will support the establishment of a high-performing Commercial field team, particularly focused on facilitating a successful brand launch. The successful candidate will ensure compliance, efficiency, and data-driven insights within field operations across our Hematology Franchise, playing a crucial role in ensuring operational readiness for product launches and ongoing excellence initiatives in the field.Key ResponsibilitiesFormulate and implement field operations strategies that align with both commercial and medical objectives.Manage field technology platforms including CRM systems, roster management, and reporting tools in collaboration with the IT department.Oversee territory design, roster management, and alignment processes to ensure compliance with coverage models.Coordinate onboarding operations with Training, HR, and Compliance teams.Direct the creation of field reports, dashboards, KPI tracking, and business insights.Ensure all field operations processes adhere to FDA, OIG, and corporate compliance standards.Lead continuous improvement initiatives aimed at enhancing scalability, efficiency, and quality.Collaborate effectively across functions including Sales, Marketing, Medical, Compliance, IT, HR, Legal, and Finance.

Feb 25, 2026

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Associate Director of Clinical Operations

Oruka Therapeutics

Full-time|$182K/yr - $208K/yr|Hybrid|Waltham, Massachusetts, United States

Oruka Therapeutics is developing biologics designed to change the treatment landscape for chronic skin conditions such as plaque psoriasis. The company focuses on long-lasting relief for patients, aiming for outcomes like disease clearance with infrequent dosing. Their pipeline includes proprietary antibodies created by Paragon Therapeutics, targeting the underlying causes of dermatologic and inflammatory diseases. More details about their work can be found at www.orukatx.com. Role overview The Associate Director of Clinical Operations will manage the setup and execution of clinical trials, supporting the Director of Clinical Operations within a specific therapeutic area. This position oversees multiple studies, combining strategic planning with day-to-day operational involvement to keep clinical programs on track and within budget. Responsibilities include handling operational details, anticipating challenges, and implementing solutions to ensure trial progress. The role requires someone who can move between leadership and hands-on work, maintaining a player/coach mindset throughout. What you will do Oversee all phases of clinical trial setup and execution across several studies Support the Director of Clinical Operations in a designated therapeutic area Balance strategic planning with direct, hands-on involvement in daily operations Identify and resolve operational challenges to maintain study timelines and budgets Requirements Demonstrated integrity and sound judgment in clinical operations Ability to shift between high-level oversight and direct involvement as needed Strong commitment to study goals and a collaborative approach Adaptability and resourcefulness in a biotech setting This hybrid role is based in Waltham, Massachusetts, with an expectation of three days onsite each week. The team values learning, growth, and a positive, inclusive culture.

Apr 22, 2026

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Associate Director of Program Leadership & Management

Deciphera Pharmaceuticals, Inc.

Full-time|On-site|Waltham

Deciphera Pharmaceuticals is excited to invite applications for the role of Associate Director of Program Leadership & Management. In this pivotal position, you will provide exceptional leadership and strategic direction to our Development and Commercial Program Teams. Collaborating closely with the Program Lead, you will be instrumental in advancing programs from early to late-phase clinical development and lifecycle management. The ideal candidate will exhibit a comprehensive understanding of drug development, thrive in ambiguous situations, and possess outstanding communication skills to foster effective collaboration within program teams and across the organization.This role demands a high level of cross-functional teamwork, engaging with both internal and external partners. You will be responsible for leading daily program management activities, including the formulation and implementation of the program's Integrated Development Strategy. A deep understanding of overall program strategy and critical path activities, as well as risk identification and mitigation planning, is essential.Key ResponsibilitiesStrategic Partnership with the Program Lead (50%)Collaborate with the Program Lead to develop and execute strategic, integrated development plans through effective leadership of Program Teams.Provide clear guidance on product development requirements to align with the expectations of external customers and business stakeholders.Monitor program progress and related KPIs, identifying gaps and risks while offering strategic recommendations.Support the execution and ongoing reassessment of development strategies in line with the overall corporate strategy.Operational Excellence Across Program Teams (50%)Facilitate program team meetings to ensure productive and efficient discussions.Ensure timely and clear communication of program strategies and progress to relevant stakeholders.Coordinate the integration of sub-teams to enhance the effectiveness of Program Teams.

Nov 17, 2025

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Scientist/Senior Scientist - Preclinical Antibody Drug Development

Biocytogen

Full-time|On-site|Waltham, Massachusetts, United States

Join the innovative team at Biocytogen, where we are dedicated to advancing the field of antibody drug development. We are actively seeking talented and driven scientists to enhance our antibody discovery team. This pivotal role focuses on optimizing therapeutic antibody binders derived from our cutting-edge RenBiologics program, which boasts a comprehensive library of therapeutic antibodies targeting a vast array of druggable genes. The ideal candidate will apply state-of-the-art antibody engineering methods to enhance binding affinity, specificity, stability, and therapeutic efficacy. Your contributions will play a vital role in the development of antibodies across multiple therapeutic domains, including immuno-oncology, inflammatory and autoimmune disorders, neurology, cardiovascular diseases, and metabolic conditions.

Jan 9, 2026

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Associate Director, CMC-Pharma Product Group

AbbVie Inc.

Full-time|On-site|Waltham

Join AbbVie as an Associate Director in our CMC-Pharma Product Group, where you will play a pivotal role in leading cross-functional teams to drive the development and manufacturing of high-quality pharmaceutical products. Your expertise will be crucial in ensuring compliance with regulatory standards and enhancing our product portfolio.

May 1, 2026

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Associate Director, Downstream, Manufacturing Sciences and Technology (Biologics)

Oruka Therapeutics

Full-time|$175K/yr - $200K/yr|Hybrid|Waltham, Massachusetts, United States

About Us:Oruka Therapeutics (Nasdaq: ORKA) is at the forefront of developing innovative biologics aimed at revolutionizing the treatment of chronic skin disorders. Our mission is to empower patients suffering from conditions such as plaque psoriasis by providing opportunities for significant disease clearance with minimal dosing frequency, potentially just once or twice a year. Leveraging a unique portfolio of advanced antibodies engineered by Paragon Therapeutics, we target the fundamental mechanisms contributing to plaque psoriasis and other dermatologic and inflammatory conditions. Learn more about our vision at www.orukatx.com.As we expand our core team, we are seeking passionate professionals who aspire to be part of a transformative journey, not just a job. If you are eager to make a positive impact and contribute to a vibrant, inclusive company culture, we want to hear from you.Job Title: Associate Director, Downstream, Manufacturing Sciences and Technology (Biologics)Location: Hybrid – Waltham, MA, with a requirement to be in-office 3 days a week.Position Overview:We are looking for a dynamic and skilled leader in Manufacturing Science and Technology (MSAT) to spearhead downstream late-stage and pivotal optimization, scale-up, and transfer of manufacturing processes. In this role, you will be responsible for process development, troubleshooting production challenges, data analysis, and ensuring adherence to regulatory standards to uphold product quality. The successful candidate will play a critical role in late-stage drug substance manufacturing and process validation activities to support BLA submissions. This position requires adaptability in a fast-paced environment, along with the ability to draft high-quality reports, finalize source documents, and actively participate in regulatory submissions. Join us as a vital member of a growing team dedicated to advancing best-in-class biotherapeutics.

Mar 30, 2026

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Associate Director of Financial Planning & Analysis

Crescent Biopharma

Full-time|On-site|Waltham, MA

The Associate Director of Financial Planning & Analysis at Crescent Biopharma is based in Waltham, MA. This role plays a key part in shaping financial planning at both the corporate and program levels, with a focus on budgeting and forecasting. Role overview This position partners with teams across the company, including R&D and Program Management. The Associate Director helps guide financial decisions that support Crescent Biopharma’s strategic goals and ongoing projects. What you will do Lead corporate and program-level budgeting and forecasting processes Collaborate with cross-functional teams to provide financial insight and analysis Support strategic planning by delivering accurate financial data and recommendations Location This role is located in Waltham, MA.

Apr 21, 2026

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Scientist/Senior Scientist in Upstream Process Development & Manufacturing (Biologics)

Oruka Therapeutics

Full-time|$130K/yr - $208K/yr|Hybrid|Waltham, Massachusetts, United States

About Oruka Therapeutics Oruka Therapeutics (Nasdaq: ORKA) develops biologics for chronic skin conditions. The company’s mission centers on helping patients with diseases like plaque psoriasis achieve lasting relief, aiming for high rates of disease clearance with infrequent dosing, sometimes just once or twice a year. Oruka’s portfolio features proprietary antibodies from Paragon Therapeutics that target the underlying mechanisms of plaque psoriasis and other dermatologic or inflammatory disorders. More information is available at www.orukatx.com. Role Overview: Scientist/Senior Scientist, Upstream Process Development & Manufacturing (Biologics) Oruka Therapeutics is hiring a Scientist or Senior Scientist to support upstream manufacturing operations in Waltham, Massachusetts. This position focuses on process development and the delivery of clinical trial materials produced at Contract Development and Manufacturing Organizations (CDMOs). The role works closely with the CMC team and collaborates with colleagues in downstream processing, analytical development, drug product, Quality Assurance, regulatory affairs, and program management. This position contributes to CMC strategy and supports the development of biotherapeutics in an innovative and growing team environment.

Apr 17, 2026

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Associate Director of Statistical Programming - Permanent Hybrid Role

ClinChoice

Full-time|Hybrid|United States

Are you looking for an opportunity to work closely with a single sponsor while benefiting from the stability and growth opportunities provided by a global CRO? Join our team at ClinChoice, where we believe it's the best of both worlds. ClinChoice is actively seeking an Associate Director of Statistical Programming for a permanent position in a hybrid work model. This role offers a unique chance to lead crucial statistical strategies within a vibrant and fast-paced environment. This position is hybrid, preferably requiring candidates to travel to our client’s location in Waltham, MA. We are looking for a seasoned Associate Director of Programming to spearhead programming initiatives, develop scalable processes, and guarantee the delivery of high-quality outputs for regulatory submissions.

Feb 5, 2026

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Associate Director, Medical Science Liaison (MSL), Rheumatology

Zenas Bio

Full-time|$181.6K/yr - $227K/yr|On-site|Waltham, MA

Zenas Bio is a pioneering clinical-stage global biopharmaceutical company dedicated to revolutionizing the treatment landscape for patients suffering from autoimmune diseases. Our strategic approach is rooted in the expertise of our seasoned leadership team, combined with a rigorous methodology for acquiring and developing promising product candidates worldwide. We are advancing two late-stage molecules, obexelimab and orelabrutinib, which we believe have the potential to provide significant clinical benefits. Obexelimab, our flagship candidate, is a bifunctional monoclonal antibody targeting both CD19 and FcγRIIb, designed to inhibit the activity of B cells implicated in various autoimmune diseases while preserving them. The unique administration method of obexelimab as a self-injected subcutaneous treatment may effectively tackle the underlying mechanisms involved in chronic autoimmune conditions. Orelabrutinib stands out as a potentially best-in-class oral Bruton’s Tyrosine Kinase (BTK) inhibitor, offering a highly selective approach to managing CNS-penetrant inflammation and disease progression in Multiple Sclerosis (MS). Additionally, Zenas is developing early-stage candidates, including an innovative oral IL-17AA/AF inhibitor and a brain-penetrant TYK2 inhibitor, both showing promise in the field.We are in search of exceptional talent who share our dedication to improving patient outcomes and possess a proven track record in the global acquisition, development, and commercialization of pharmaceutical products. Join our fast-paced environment where you will have the chance to grow both personally and professionally while contributing to our mission of leading the charge in immunology and autoimmune disease treatment, grounded in our core values of Transparency, Relationships, Urgency, Excellence, and TRUE Innovation!Territory: MidAtlantic (NY, NJ, PA, OH)Position Summary:The Associate Director, Medical Science Liaison (MSL) for Rheumatology at Zenas Bio serves as the field-based representative of our Medical Affairs team. MSLs are scientifically trained professionals with robust clinical and scientific backgrounds, committed to providing the healthcare community with balanced, scientifically rigorous information. This role reports directly to the Executive National Director of US MSLs.Key Responsibilities:Identify, establish, and nurture professional relationships with international, national, regional, and local key opinion leaders and allied healthcare professionals.

Apr 7, 2026

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Scientist II - Innovative Research Role

Artech Information Systems LLC

Contract|On-site|Waltham

Join our dynamic team at Artech Information Systems LLC as a Scientist II, where your expertise will contribute to cutting-edge research and innovation. We are seeking a detail-oriented and motivated individual to engage in scientific projects that push the boundaries of technology and discovery.

Jan 25, 2016

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Scientist II

Artech Information Systems LLC

Contract|On-site|Waltham

Join Artech Information Systems LLC as a Scientist II, where you will play a pivotal role in advancing our innovative solutions. As a mid-senior level scientist, you will be involved in cutting-edge research and development projects, utilizing your expertise to drive results and contribute to our team's success.

Jan 26, 2016

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Scientist II

Artech Information Systems LLC

Contract|On-site|Waltham

We are seeking a highly skilled and motivated Scientist II to join our dynamic team. In this role, you will leverage your expertise to contribute to innovative research and development projects. The ideal candidate will possess a strong background in scientific methodologies and a passion for advancing knowledge in their field.

Jan 18, 2016

Scientist II

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