The Biomedical Clinical Scientist is responsible for scientific oversight, data integrity and quality of clinical trial(s) in support of the development strategy for programs within the clinical development. ROLE RESPONSIBILITIES • Clinical scientist for assigned studies maintaining current scientific and clinical knowledge in the specific therapeutic and disease area(s) of assignment. • Effectively partners with other clinical and medical colleagues, clinical operations and other functional lines for the successful implementation and execution of the clinical trial(s) within the assigned program. • Responsible for scientific oversight, data integrity and quality of the clinical trial(s). • Represents the study team in governance meetings and submissions, partners with/supports the clients Development lead/Medical Director regarding study and disease area strategy. • Support Authoring protocols, study level informed consent documents, and contributes to authoring of IBs, site training materials, clinical study reports, regulatory responses, and other clinical and regulatory documents; supports preparations for Health Authority meetings, participates as appropriate. • Sets the clinical data review strategy and leads the team in the collection of quality data and review of emerging clinical data and trends; reviews and queries data; presents and discusses relevant data to appropriate teams, governance bodies, and other internal and external stakeholders. • In close partnership with medically qualified colleague/s, analyzes the emerging safety profile of the drug, keeping the clinical and safety colleagues informed of changes in the safety profile as they occur in the assigned trial(s). • Follows relevant SOPs and regulations, has an excellent understanding of and complies with applicable trainings, seeks opportunities to further improve quality and efficiency of clinical procedures; leads or actively participates in portfolio- and client level workgroups aimed at optimizing clinical development procedures; may be a subject matter expert for a relevant SOP or procedure. QUALIFICATIONS • Science degree (PhD, PharmD, or equivalent) and minimum of 7-year Clinical Research experience in Pharma-Biotech/CRO, OR BA/BS and minimum of 10-year Clinical Research experience in a similar role in industry/CRO. • Clinical Research experience in the phase 3/pivotal space across various therapeutic areas, ideally on the side of the Pharma/Biotech and with a track record of successful regulatory submission, inspection, and regulatory approval. • Excellent knowledge of clinical procedures, ICH guidelines, GCP and familiarity with FDA, EMA, and global regulations. • Demonstrates a passion for helping patients with cancer and for the science of oncology, Inflammation and rare diseases. • Proven analytical skills with the ability to work on large data sets. • Effective communication, presentation, and organizational skills to ensure coordinated and timely delivery. • Demonstrated scientific writing skills and excellent communication skills (written and spoken) in English; scientific productivity via publications, posters, abstracts and/or presentations. • Embraces evolving technologies and adopts best practices aimed at improving the efficiency and quality of clinical development; proficient with basic IT; efficiently using a computer and telecommunications • Has a global collaborative perspective and mindset works well in a diverse team environment with colleagues from diverse cultures, backgrounds, and geographies. both as a leader and a key contributor; works effectively with internal and external partners and investigators/medical professionals. • Has extensive understanding of related disciplines, e.g., clinical operations, safety, biostatistics, regulatory, study management, pre-clinical, pharmacology, quality assurance. • Candidate demonstrates a breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact.