The Senior Medical Director, Clinical Development will be an essential contributor to the scientific, clinical, and operational scope of clinical development programs with an emphasis on study and program-specific activities. . The Senior Medical Director, Clinical Development will drive the design, planning, and implementation of study protocols for assigned investigational products and will play a key role in supporting related regulatory activ...
This is a full-time, one year contract role. . The Sr. Clinical Data Analyst will be responsible for creating fit-for-purpose analyses, visual data displays and dashboards from diverse data types to aid in internal data consumption and decision-making. This position will report into the Head of Clinical Data Sciences and will interact regularly with diverse stakeholders across the organization. Demonstrated abilities to prioritize work. to unders...
Summary. . The. Talent Acquisition. Specialist. is expected to be a conceptual thinker with fantastic organizational. . time management. . administrative and IT. skills. with the ability. to. adapt in a fast-paced environment. . To ensure success. having. strong problem solving and decision-making skills, effective at. multi-tasking. and. a. good understanding of the. recruitment process. is key. . Responsibilities. . Schedule interview. s. for o...
This is a full-time, one year contract role. . The Sr. Clinical Data Analyst will be responsible for creating fit-for-purpose analyses, visual data displays and dashboards from diverse data types to aid in internal data consumption and decision-making. This position will report into the Head of Clinical Data Sciences and will interact regularly with diverse stakeholders across the organization. Demonstrated abilities to prioritize work. to unders...
Summary. . The. Talent Acquisition. Specialist. is expected to be a conceptual thinker with fantastic organizational. . time management. . administrative and IT. skills. with the ability. to. adapt in a fast-paced environment. . To ensure success. having. strong problem solving and decision-making skills, effective at. multi-tasking. and. a. good understanding of the. recruitment process. is key. . Responsibilities. . Schedule interview. s. for o...
The Principal, Clinical Scientist will be an essential contributor to the scientific, clinical, and operational scope of clinical development programs with an emphasis on protocol-specific activities. The Principal Clinical Scientist will help drive the design, planning, and implementation of study protocols for assigned investigational products and will play a key role in supporting related regulatory activities. This role will work on cross-fun...
The Principal, Clinical Scientist will be an essential contributor to the scientific, clinical, and operational scope of clinical development programs with an emphasis on protocol-specific activities. The Principal Clinical Scientist will help drive the design, planning, and implementation of study protocols for assigned investigational products and will play a key role in supporting related regulatory activities. This role will work on cross-fun...
This position will provide technical outputs for the Small Molecule Analytical Sciences function within Arcus’ Pharmaceutical Development & Manufacturing organization. This onsite role will include laboratory testing responsibilities (non-GMP) in support of drug substance and drug product development. . This is a 1 year, 40 hour per week contract lab based 5 days a week in Hayward, CA. Seeking a collaborative mindset. . Responsibilities. Analysis...
The Sr. Clinical Trial Manager (CTM) Contractor will provide clinical study support to the Clinical Program Manager/Study Management Team Lead (SMTL) for one or more clinical studies, ensuring efficient delivery of clinical trials in a matrix environment. Key accountabilities include assuring successful conduct of clinical studies consistent with applicable regulations, guidelines and procedures, as well as supporting clinical project timelines, ...
The. Executive. Medical Director, Clinical Development will be an essential contributor to the scientific, clinical, and operational scope of clinical development programs with an emphasis on study and program-specific activities. . The. Executive. Medical Director will drive the design, planning, and implementation of study protocols for assigned investigational products and will play a key role in supporting related regulatory activities. . Thi...
Description. The primary responsibility for this position is to support quality oversight of change control and validation activities as related to regulated computer systems for 21 CFR Part 11 compliance. This individual will also work closely with internal stakeholders on improvement of Veeva platform systems for supporting various key quality processes such as internal/external audits, change control, deviation/CAPA, inspection management, pro...
Summary. . This position. will be. responsible for. developing. and implementing. comprehensive. worldwide patent strategies. and communicating. intellectual property. (IP). considerations. to multiple stakeholders. . . Responsibilit. ies. . Collaborate with scientific colleagues to. create. IP. strategies. which. drive business value. Prepare. high quality patent applications with the assistance of outside counsel. Develop a deep understanding o...
