BioSpace, Inc.
Associate Medical Director, Clinical Science, GI TAU
BioSpace, Inc., Cambridge, Massachusetts, us, 02140
Associate Medical Director, Clinical Science, GI TAU
Join us as an
Associate Medical Director, Clinical Science, GI TAU
at
BioSpace . Job Overview
Position based in Cambridge, MA, focused on leading and driving global clinical development strategies within Takeda's Gastrointestinal & Inflammation Therapeutic Area Unit. Key Responsibilities
Lead clinical teams as Global Clinical Lead or represent Clinical Science on project teams. Support the development of clinical strategies, protocols, and regulatory submissions. Monitor and interpret clinical data, make development decisions, and adapt strategies accordingly. Oversee clinical study design, execution, and data interpretation. Manage external relationships with key opinion leaders and regulatory agencies. Evaluate potential business opportunities and lead negotiations for alliances or in-licensing. Lead and mentor staff, participate in internal task forces and cross-functional teams. Qualifications
MD or equivalent with at least 5 years of relevant clinical research experience. Experience leading matrix teams and cross-functional collaboration. Strong communication, negotiation, and strategic planning skills. Knowledge of regional/global regulatory requirements and GCP/ICH guidelines. Additional Information
This role is classified as a hybrid position per Takedas policy. Compensation ranges from $194,800 to $306,130, depending on experience and qualifications. Takeda is an equal opportunity employer committed to diversity and inclusion. #J-18808-Ljbffr
Join us as an
Associate Medical Director, Clinical Science, GI TAU
at
BioSpace . Job Overview
Position based in Cambridge, MA, focused on leading and driving global clinical development strategies within Takeda's Gastrointestinal & Inflammation Therapeutic Area Unit. Key Responsibilities
Lead clinical teams as Global Clinical Lead or represent Clinical Science on project teams. Support the development of clinical strategies, protocols, and regulatory submissions. Monitor and interpret clinical data, make development decisions, and adapt strategies accordingly. Oversee clinical study design, execution, and data interpretation. Manage external relationships with key opinion leaders and regulatory agencies. Evaluate potential business opportunities and lead negotiations for alliances or in-licensing. Lead and mentor staff, participate in internal task forces and cross-functional teams. Qualifications
MD or equivalent with at least 5 years of relevant clinical research experience. Experience leading matrix teams and cross-functional collaboration. Strong communication, negotiation, and strategic planning skills. Knowledge of regional/global regulatory requirements and GCP/ICH guidelines. Additional Information
This role is classified as a hybrid position per Takedas policy. Compensation ranges from $194,800 to $306,130, depending on experience and qualifications. Takeda is an equal opportunity employer committed to diversity and inclusion. #J-18808-Ljbffr