Maintain and culture multiple cell lines Participate in protocol development and optimization of cellular assays Conduct reporter assays to assess cellular signaling events Regularly perform gene expression, protein detection analysis Maintain accurate and detailed laboratory records Collaborate with team members on research projects Qualifications Currently enrolled as a

Implementing statistical analyses using SAS and performing quality review of SAS programs and deliverables for in house analyses as well as out sourced programming deliverables Build SAS datasets from clinical databases, external data sources, and other data sources, utilizing SDTM and ADaM guidelines. Produce and/or validate tables, listings, figures, and analysis datase

Technical Support and Troubleshooting Provide the highest level of technical support and guidance to research teams, addressing both hardware and software issues. Work closely with researchers to integrate new technology and tools that enhance research capabilities. Train staff on new IT systems and best practices. System Administration & Integration Install, configure, a

Independently author, review, and manage clinical documents as the lead medical writer. Lead strategy discussions for document development and contribute to medical writing process development. Manage contract medical writers. Primary Responsibilities Independently authors high quality, scientifically accurate, complex clinical documents, ensuring consistency between rela

Lead the biostatistics team, including recruiting, developing, and retaining top talent Lead the development and delivery of statistical methodology, biostatistical subject matter expertise, statistical tools/applications development to support the development and marketing of new medicines Partner with key stakeholders/functions to ensure the timely delivery of high qual

TheCTA is responsible forsupporting the Clinical program teams and may assist the teams across multipleclinical studies. The CTA would also participate in broader clinical operationsactivitiesand initiatives such as the development and refinement of new processes. Responsibilities Clinical Study and Program Support ~70% Support clinical study teams in the delivery of key

Signal detection, evaluation, and management from clinical trials Perform data analysis to evaluate safety signals and write up/ present analysis and results Collaborate with other applicable functional areas, including but not limited to Biostatistics, Clinical, Quality, Regulatory Affairs to identify, evaluate and manage safety signals Assure oversight for the review of

Ensures high quality and on time submissions, including for INDs, IMPDs, CTAs and BLAs, that align with company strategies and Health Authority requirements. This includes planning, coordination and tracking the CMC dossier towards submission milestones. Interact with cross functional departments to ensure deliverables are met according to the corporate goals. Coordinate

The Senior Director, Scientific Communications is a seasoned Medical Affairs professional with an established track record of creating, leading, and delivering high impact scientific publication and communication program(s). S/he will oversee publication planning and execution along with being an integral part of Program Team(s) across the Keros portfolio. Areas of focus

Perform in vitro and ex vivo research bench work RNA isolation and expression analysis by qRT PCR Perform in vitro assays to confirm the expression and activity of candidate therapeutic proteins (Western Blot, ELISA) Perform antibody staining and flow cytometic analysis of hematopoietic cells Maintain clear, accurate records of lab work and summarize results as needed in

As a Director/Senior Director of Toxicology , you will play a critical role in ensuring the safety and efficacy of our pharmaceutical biologics. You'll lead and oversee toxicology programs, from target identification to GLP (Good Laboratory Practice) toxicity studies, supporting clinical development and eventual market approval. Your expertise will be essential in identif

We are seeking a Sr. Manager/Associate Director MSAT Drug Substance to join our team. The ideal candidate will have a deep understanding of biologics drug substance production (upstream and downstream), tech transfer, and regulatory submission support. The candidate will engage and work with external partners (CDMOs) to ensure successful cGMP manufacturing campaigns and p