Clinical Operations Head Salary at Lantheus Medical Imaging Inc BETA

COMPANY OVERVIEW AIRNA is a biotechnology company with a mission to transform lives, one RNA edit at a time. AIRNA is pioneering the discovery and development of RNA editing therapeutics to realize the therapeutic potential of base editing for patients with rare and common diseases. RNA editing modality is poised to lead the next generation of RNA therapeutics by bringing the precision of gene editing technology with a potent and safe medicine that can be conveniently re-dosed and manufactured. Our RESTORE+™ platform is based on groundbreaking research by academic co-founders Thorsten Stafforst (University of Tübingen) and Jin Billy Li (Stanford University), who were the first to elucidate a therapeutic approach for precise editing of RNA. AIRNA has received $90 million in Series A financing from world class venture capital firms, including Forbion and Arch Venture Partners, and is headquartered in Cambridge, MA with research operations in Tübingen, Germany. JOB DESCRIPTION The Head of

At HAYA Therapeutics, we are revolutionizing RNA-guided genome-targeting therapies to treat fibrosis, heart failure, and other serious diseases associated with aging. Our innovative platform leverages long non-coding RNAs (lncRNAs)—key regulators within the “dark matter” of the genome—to develop first-in-class, highly specific therapies that modulate gene expression and restore cellular function. Recognized for our innovation, HAYA received the prestigious Innosuisse Certificate for Sustainable Growth and has been nominated as TOP Innovative Companies in Switzerland 2025. As a fast-growing biotech, we offer an entrepreneurial, science-driven environment where you’ll have a direct impact on shaping our pipeline and advancing RNA medicine. We are a collective of scientific-minded professionals who thrive on curiosity, collaboration, and the relentless pursuit of progress. We’re committed to making Haya the best place you’ll ever work - where your growth is just as important as our shared

Location: Bedford, MA (Onsite) Focus: Rare Disease Job Overview: The Clinical Trials Manager oversees moderate-complexity clinical trial execution, ensuring adherence to protocol, budget, and regulations, while addressing issues and supporting process improvements. Primary Job Responsibilities: Oversees Phase 1-3 clinical studies, ensuring adherence to timelines, budgets, and plans with CRO and vendor collaboration. Leads the selection and qualification of Investigators and vendors. Contributes to the development of clinical study protocols and documents. Develops operational plans and maintains timelines through coordination with internal teams. Identifies and mitigates study risks, ensuring alignment with stakeholder expectations. Manages drug supply coordination with CMC for consistent site delivery. Assists in budget management and financial forecasting for resource allocation. Enhances operations through project management skills, improving performance and SOPs. Primary Job Requir

Director, Quality Systems Job Type: Permanent Location: Waltham, MA. Site based Salary: Up to $230K + Bonus + Benefits The company is a cutting-edge clinical-stage biotechnology company mainly dedicated to the Nephrology space. They have a dynamic pipeline of groundbreaking therapies. As the Director, Quality & Compliance, you will take a leading role in advancing and overseeing the Quality Management System to align with relevant global regulatory standards and company business goals. This position offers significant visibility within the organization. Responsibilities Oversee companywide GxP training programs, aligning training requirements with job functions. Lead the development and maintenance of the audit and inspection readiness programs. Contribute to the continuous improvement of the inspection readiness program and new initiatives. Develop, review, and monitor quality agreements and contracts. Manage GxP Training, Supplier Management, and documentation systems. Support the Qu

Position Summary: The Associate Director, Quality will be responsible for the development, management and continuous improvement of Quality Systems at Upstream to ensure its products and processes are compliant to regulatory, functional area and customer requirements. Partner with all areas of the business to understand and address their needs/issues. Interface with all areas of the business to elevate potential issues to management and drive continuous improvement efforts. Provide expertise and leadership in implementing a quality system management function for clinical and commercial products. Key Responsibilities: Provide Expertise on implementation and maintenance of the QualityManagement System (QMS), both electronic and paper based, including but not limited to SOPs, document control,product complaints, training, change management and quality event management (deviations and CAPAs) Administer documents for clinical and commercial operations that are compliant and fit for purpose.

We are hiring a Statistical Programmer Consultant on a contract basis. This role will be remote based. This is a W2 position. The Consultant will provide timely support to the project team on all statistical programming matters according to the project strategy. Programs SDTM/ADaM/TLFs for the studies, write datasets specification, QC datasets and tables. Identifies and communicates changes in project requirements that may affect key deliverables. Responsibilities Involved in the programming activities on multiple projects/ studies across various therapeutic areas, both internally and externally by CROs Creates and reviews annotated CRF to SDTM datasets Provides support in balancing conflicting priorities, promoting communication and adequate information flow to motivate, encourage and align people with the company' s strategic objectives Functions as a positive role model for setting high expectations for quality, creativity and project ownership Works collaboratively with Clinical Op

**By joining Bio-Techne, youll join a company with a powerful and positive purpose of enabling cutting-edge research in Life Sciences and Clinical Diagnostics. Bio-Techne, and all of its brands, provides tools for researchers to further treat and prevent disease worldwide.** By joining Exosome Diagnostics, a Bio-Techne brand (NASDAQ: TECH), you will have an impact on future cutting-edge research. Exosome Diagnostics is a liquid biopsy company that harness the power of Exosomes as a multi-analyte component of Liquid Biopsies. Bio-Techne, and all of its brands, provides tools for researchers in Life Sciences and Clinical Diagnostics. **Schedule:** Monday Friday, Possible Saturday **The Opportunity** This position will be responsible for planning and executing on partnered development projects for both internal and external collaborations. Technology transfer, operationalization, verification, and validation, of nucleic and protein assays are all in scope. Secondary responsibilities may i

Manager, Clinical Operations SanegeneBio Woburn, MA Company Overview: SanegeneBio is a clinical-stage biotechnology company developing innovative RNAi-based genetic medicines. Our proprietary LEAD™ (Ligand and Enhancer Assisted Delivery) RNAi platform drives a growing pipeline across cardiometabolic and complement-mediated diseases. With R&D operations in Boston, Suzhou, and Shanghai, we are committed to scientific excellence, integrity, and collaboration. Position Overview: We are seeking a highly organized and experienced Clinical Operations Manager to join our dynamic clinical research team. The ideal candidate will possess a robust background in managing clinical trials, particularly in the areas of nephropathies, including IgA Nephropathy (IgAN), C3 Glomerulopathy (C3G), and other related kidney diseases. This role will involve overseeing the planning, execution, and management of clinical trials, ensuring compliance with regulatory requirements, and maintaining high standards of