This role requires 3 days onsite in Cambridge, MA - Must be local or willing to relocate. Role responsible for operational activities, and leadership for the execution of the assigned clinical studies (Phases I-IV) under supervision. The role. Manages day-to-day activities of all aspects for the management of clinical studies, including study plans, timelines, resources, allocation and management of product (re-)supply, problem identification and...
This role requires 3 days onsite in Cambridge, MA - Must be local or willing to relocate. Role responsible for operational activities, and leadership for the execution of the assigned clinical studies (Phases I-IV) under supervision. The role. Manages day-to-day activities of all aspects for the management of clinical studies, including study plans, timelines, resources, allocation and management of product (re-)supply, problem identification and...
Senior Director level role that identifies unmet medical needs and develops medical plan to support development and commercialization of products. Leverages medical and scientific insights to develop medical plan for product(s) in hematologic malignancies, hematology and oncology area. Generates data plan, medical publication plan, and medical education plan to support development and commercialization of organization’s products (the Medical Affa...
To promote proper use by conducting necessary internal and external communication such as consultation with the domestic regulatory authority so that safety measures planned based on the risk/benefit evaluation of each product can be appropriately implemented based on the developed PV plan. To develop human resources for appropriate business operations and enhance organizational capabilities by improving the problem-solving skills and mutual assi...
Medical Director level role that provides strategic oversight for clinical development programs and associated clinical trials. Ensures the highest medical integrity and conduct of clinical studies in the execution and completion of the clinical and regulatory components of the program. Enhances and streamlines programs in the Clinical Development organization. Develops proactive strategies to prevent risk and promote safety of patients enrolled ...
Senior Director level role that identifies unmet medical needs and develops medical plan to support development and commercialization of products. Leverages medical and scientific insights to develop medical plan for product(s) in hematologic malignancies, hematology and oncology area. Generates data plan, medical publication plan, and medical education plan to support development and commercialization of organization’s products (the Medical Affa...
To promote proper use by conducting necessary internal and external communication such as consultation with the domestic regulatory authority so that safety measures planned based on the risk/benefit evaluation of each product can be appropriately implemented based on the developed PV plan. To develop human resources for appropriate business operations and enhance organizational capabilities by improving the problem-solving skills and mutual assi...
Medical Director level role that provides strategic oversight for clinical development programs and associated clinical trials. Ensures the highest medical integrity and conduct of clinical studies in the execution and completion of the clinical and regulatory components of the program. Enhances and streamlines programs in the Clinical Development organization. Develops proactive strategies to prevent risk and promote safety of patients enrolled ...
Role responsible for collaborating with and utilizing instructions/information from study managers or global project leaders to support Clinical Operations by ensuring the timely and effective implementation and maintenance of the clinical operational study documentation, in accordance with study timelines from study initiation through to study closeout. The role. Prepares, processes, distributes, updates and maintains (filing and archiving) clin...
