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Lead exploration and application of advanced AI models, develop and deploy AI solutions, and lead MLOps processes. | Experience with state-of-the-art NLP algorithms, cloud platforms, Python, and customer-facing roles. | We are looking for someone that has been in a customer facing role and worked on projects similar to ChatGPT; experience with genAI videos and genAI product design. AI Architect Responsibilities: • Work in a team of machine learning engineers of different specializations to prototype and ship world class algorithms that are state of the art. • Lead the exploration and application of Large Language Models and Generative AI, venturing into new areas within these fields, including multi modal capabilities. • Lead MLOps, automating ML pipeline, including the training, testing, deployment, monitoring, and scaling of AI models. AI Architect Requirements: • NLP/AI Building Software to release to customers • Experience with Cloud Technologies- AWS and GCP preferably • Experience with state-of-the-art NLP algorithms and AI models, Multi-modal LLMs, Multi-modal contrastive learning, Foundation models, Diffusion based models and parameter efficient fine tuning of LLMs • Programming- expertise in programming languages such as Python • Strong Customer Facing experience Department: Preferred Vendors This is a part time position

Lead and oversee global clinical programs, ensuring high-quality data collection, regulatory compliance, and strategic integration of clinical development plans. | PhD/MD/PharmD with 10+ years biopharma drug development experience including clinical trial leadership, strategic planning, and regulatory knowledge. | As Head of Medical Science, you will play a critical role in shaping the scientific vision and medical strategy of our client. Reporting directly to the Chief Medical Officer, you will lead efforts to bridge clinical science and pre-clinical development, ensuring alignment with our mission to deliver transformative therapies to patients. This involves high level strategic planning as well as significant hands-on responsibilities to support our growing pipeline. Core responsibilities include overseeing the design, oversight, and reporting of clinical trials that meet the highest standards of excellence for ethics, scientific merit, and regulatory compliance. Key Responsibilities • Management of overall study planning, study execution, and delivery of multiple global clinical programs. Including but not limited to oversight of and accountability for the collection of high-quality clinical data. • Oversee review and interpretation of efficacy and safety data. Contribution to clinical trial safety oversight by participating in safety review and analysis of clinical trial data consistent with Safety Review Plan. • Close collaboration with Clinical Operations, Toxicology/Pharmacology, Preclinical, Regulatory, Biostatistics, and outside contractors to ensure the successful strategic integration of clinical development plans and strategies. • Contribute to authoring, review, and approval of required clinical study protocols, clinical study reports (CSRs), sections of regulatory documents such as Investigators' Brochures, briefing books, safety updates, IND/CTA submission documents, and responses to Health Authorities' questions. • Collaboration with CMC/clinical suppliers to provide clinical trial supply assumptions and contribution to design and packaging of supplies for clinical trials. • Communication with internal and external teams in a high impact, highly visible fashion through written and verbal means. Qualifications: • PhD, PharmD, or MD • Minimum 10+ years of biopharmaceutical industry drug development experience, early through late-stage development, including the design and conduct of early and late phase clinical studies. CNS/Neuroscience experience strongly preferred. • Proven ability to lead a multidisciplinary team toward a successful outcome. • Previous experience successfully leading a clinical development team/matrix team with responsibility for studies in multiple geographic regions. • Excellent strategic and project management skillset with drug development programs • Ability to work with the Senior Management Team and other external audiences such KOLs and regulatory bodies. • Ability to thrive in highly entrepreneurial biotech environment, with some prior experience in a small/medium size company an advantage. • "Hands-on", "roll-up-the-sleeves" when necessary, leader who understands the need for involvement in a small company environment while recognizing when to delegate and seek results from the team. • Thorough understanding of country-specific, FDA (and equivalent), ICH and GCP guidelines as well as cross-functional clinical processes including data management, pharmacovigilance, biostatistics, medical writing, and study reporting. • Excellent interpersonal, communication, negotiation and influencing skills. • Experience having managed significant accelerations and challenges in clinical programs is desirable. • Ability to travel domestically and international (up to 10% of the time)

Support clinical quality team with data management, issue resolution, reporting, and process improvement to enhance patient care quality and compliance. | Bachelor's degree, 2+ years relevant experience, healthcare or clinical setting preferred, proficiency with Microsoft Office and data platforms like Salesforce. | Job Overview: We are looking for a detail-oriented and proactive Clinical Quality Associate to support our Clinical Quality team. This role is integral to assisting the Clinical Quality Manager and enhancing clinical processes aimed at improving patient care quality, provider satisfaction, regulatory compliance, and overall safety. You will be responsible for accurate data collection, effective issue resolution, and timely reporting to maintain and elevate clinical standards. Key Responsibilities: • Provide administrative and data management support to the Clinical Quality Manager and team. • Maintain clinical data systems, including managing the Salesforce dashboard and associated workflows. • Address and respond to patient inquiries, privacy concerns, reportable events, provider requests, and patient care cases swiftly and accurately. • Collect, organize, and analyze data related to clinical quality, patient safety, and incident reporting. • Investigate patient and client complaints to facilitate timely and effective resolution. • Collaborate with internal teams to prioritize and handle client requests and feedback. • Deliver timely and accurate reports to both internal and external stakeholders. • Assist in developing and implementing processes to improve clinical quality and compliance. • Perform additional duties and special projects to support clinical quality goals. Qualifications: • Bachelor's degree or equivalent experience in a related field. • Minimum of 2 years of relevant work experience; healthcare or clinical setting experience is a plus. • Knowledge of medical terminology and coding is beneficial but not essential. • Strong organizational and analytical skills with attention to detail. • Ability to adapt quickly in a fast-paced environment while meeting deadlines. • Excellent communication, problem-solving skills, and the ability to work independently and within a team. • Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint) and experience with data management platforms (e.g., Salesforce). • Interest in healthcare, clinical quality, and emerging technologies. This is a contract position