- Medtronic (Boston, MA)
- …**at Sr and Prin levels)** + Practical and demonstrated knowledge of project /program management practices desired for Senior and Principal Levels with the ... plan for educational programs for new and tenured sales representatives and clinical specialists to drive electrophysiology (EP) product procedure across the CAS… more
- Otsuka America Pharmaceutical Inc. (Boston, MA)
- …with 2 years' experience in regulatory affairs or related areas (eg, clinical development, project management, quality assurance, etc.) in pharmaceutical or ... associated regulatory challenges to the GRL, global regulatory team, assigned project teams, and internal/external functional business units as needed. Works… more
- Pfizer (Cambridge, MA)
- **ROLE SUMMARY** The Sr . Director, AI & Data is responsible for directly overseeing and organizing wide-reaching Pfizer initiatives through digital-wide initiatives, ... impact is through your direct work. As a people manager , you are responsible for leading and directing your...technical SME's towards a common technical vision. + Advise Senior leadership on emerging technology landscape externally and internally… more
- Beth Israel Lahey Health (Burlington, MA)
- …receives general oversight; support of research initiatives, regulatory guidance 3 . Sr . Clinical Research Coordinator / Clinical Research Coordinator ... providing mentoring, direction and guidance to research staff (eg, Clinical Research Coordinators). **Job Description:** **Essential Duties & Responsibilities**… more
- Bristol Myers Squibb (Devens, MA)
- …lives. Read more: careers.bms.com/working-with-us . **Position Summary** The ** Sr . Director, Analytical Science and Technology (ASAT) Analytical Excellence** ... platforms and enterprise software systems used in QC testing + Strong project management and organizational skills, able to coordinate multiple initiatives across… more
- Parexel (Boston, MA)
- …create, and edit all documents associated with clinical research. The Senior Medical Writer may operate as the project lead writer/submission coordinator ... contributions of multiple writers working on related documents. The Senior Medical Writer also facilitates process improvement and technical...level of training or performance of team members on project work. Provide line manager with input… more
- Parexel (Boston, MA)
- …content review. **Document Project Management** + Act in the capacity of project manager /lead for medical writing projects, which may entail serving as the ... **Job Summary:** The Senior Medical Writer will research, create, and edit...will research, create, and edit all documents associated with clinical research. Responsibilities also include: acting as primary client… more
- Parexel (Boston, MA)
- …+ Communicating and discussing issues related to review process with Line Manager / Project Leader/Designee + Interacting with internal and external stakeholders ... Join our dynamic Patient Safety team as a ** Senior Physician** where you'll leverage your medical expertise...medical expertise to ensure the safety of patients in clinical trials and post-marketing settings. In this pivotal role,… more
- CenterWell (Boston, MA)
- …**Roadmap Management** + Own and evolve the product roadmap for the clinical vertical, collaborating with senior leaders to ensure strategic alignment. ... Lead a dynamic team of product management professionals dedicated to advancing clinical operations and technology solutions. Drive the strategic roadmap for the … more
- Deloitte (Boston, MA)
- Healthcare Clinical Documentation Specialist - Senior Consultant Our Deloitte Regulatory, Risk & Forensic team helps client leaders translate multifaceted risk ... + Strategic Risk: Helping clients to embrace their most significant regulatory, clinical documentation, and operational risks, by enabling senior health care… more