Director, Clinical Jobs Near Waltham, MA

This individual will work in a highly matrixed team setting and ensures close collaboration with other PDT BU functions and relevant Takeda R&D functions to support project goals...

Building relationships with opinion leaders and through external alliances for partnered products when relevant, Presentation of data and scientific information to the organization and externally at a...

Ensure that goals and objectives for clinical development programs are met by providing strategic and tactical input by developing program specific goals, tracking metrics, producing and presenting su...

We are seeking a Director, Clinical Scientist, to play a pivotal role in supporting key oncology programs. This position will report to the VP, Head of Medical...

Plan, design, execute and report program-specific clinical pharmacology studies by working cross-functionally with Clinical Operations and Clinical Research. Work collaboratively with CRO’s/external...

Provide strategic input, management and oversight of clinical development pipeline across all therapeutic areas, managing several phase I/Ib/II and clinical pharmacology studies simultaneously...

Responsible to identify study/program issues by reviewing and monitoring emerging clinical safety and efficacy data; Develop sound, strategic solutions to issues and lead issue resolution...

Develop and implement medical/scientific strategy through strong engagement and learning from medical/KOL and patient communities

Maintain a high level of clinical and scientific expertise in the disease area(s) by reviewing the literature, attending medical/scientific meetings, and through personal interchanges with consultants...

Strategic guidance to phase 1-3 development programs and oversight of global clinical trial team(s) on assigned program(s). Protocol development from concept to final protocol...

Integrate the scientific rationale, regulatory requirements, product development plan, and commercial goals to build a solid strategic framework for the Clinical Development Plan (CDP). Establish appr...

Contributes to the business operations of the department by reviewing P&L statements, contributing to the budget planning for proposed initiatives, and overseeing that clinical and education activitie...

Responsible for overseeing the coordination, management, and operational aspects of Clinical Programs to secure the successful completion of projects within prescribed time frame and funding parameter...

Interact frequently with investigators to share new scientific and clinical data and maintain enthusiasm and engagement to optimize clinical trial enrollment...

Manage GCDM personnel, priorities, and workload on the preparation, validation, processing, reviewing, querying, dictionary coding, and maintenance of clinical data on individual clinical trials and r...

Supervise closely all major written deliverables (regulatory submissions, original articles, abstracts), and presentation materials.

Responsibilities: Develop multi-touch, multi-channel demand generation programs from concept to execution

Generating the data and evidence required to determine a medicine’s potential efficacy, safety profile, key areas of product differentiation and value to patient in the shortest possible timeframe; ga...

Lead the design and delivery of IT solutions to support business requirements. This will involve direct stakeholder interface with regards to development, design, delivery, testing, validation, and tr...

Responsible for representing Clinical Operations on cross-functional project teams and vendor/CRO operational meetings and ensuring compliance with operational standards and procedures...

Proven ability to design, manage and interpret outsourced non-clinical safety studies in rodent and non-rodent (NHP) species

Collaborate closely with clinical operations and be accountable for clinical trial conduct and timelines for associated key deliverables.

Develops and maintains strong knowledge of best regulatory practices, clinical pharmacology principles, PK/PD analysis methodology and drug development precedent...

Will be required to line manage other Clinical Scientists including project allocations/resource management, recruitment & selection, personal development and performance management; may be required t...

Responsible for the design, planning, oversight as well as the analysis, interpretation and reporting of results of Clinical Pharmacology studies.