TRABAJO GLOBAL REGULATORY SUBMISSIONS PROJECT BARCELONA, BARCELONA

The rid will work closely with therapeutic area (ta) vp, executive regulatory science directors, global regulatory leaders (grls) and regulatory affairs directors...

Specialized focus on digital regulatory science, clinical medical affairs, pv (pharmacovigilance), sustainability, and other science-related project activities...

Portfolio strategy: contribute to the broader therapeutic area strategy global commercialization strategy development: formulate and implement global commercialization...

The global development medical director and counterpart global development scientist work collaboratively in the clinical aspects underpinning a product...

The candidate will lead all regulatory submissions... broad understanding of the evolving clinical landscape in hematology/oncology lead the overall development...

Establish key relationships internally with clinical project teams, and externally with regulatory bodies and external service providers...

Demonstrated project management skills... the employee carries out this role in accordance with departmental sops, corporate policy and other legal and regulatory...

Transperfect has global headquarters in new york, with regional headquarters in london and hong kong... more than global organizations employ transperfect’s globallink®...

Provide expert scientific input into the preparation of regulatory documents and interactions with regulatory authorities... the objectives of the global development...

You will provide expert medical input into the preparation of regulatory documents and interactions with regulatory authorities... as a global development medical...

Provide/roll out guidance and training to the western europe business relating to regulatory requirements... accountabilities include: work with manufacturing plants...

• manage product transfer projects both in coordination with plant consolidations and as a separate project... as a diverse, global team, we work together to solve...

Key responsibilities: • providing expert safety input to the clinical development program for assigned projects/products, participating as an active member of the...

• extensive knowledge of clinical research regulatory requirements (incl ich-gcp) and demonstrated abilities in clinical study management processes and clinical/drug...

Supports or leads interactions with global medical affairs, marketing companies, commercial, and regulatory functions in collaboration with gch/gcpl to ensure cross...

• lead cross-functional teams, manage resources, and maintain project schedules and budgets... • review engineering designs & drawings, construction and commissioning...