Senior Clinical Data Manager Jobs in Cambridge, MA

Novo Nordisk - Cambridge, MA

of therapeutic drug programs from preclinical through clinical stages across the relevant assessment areas: proposed clinical benefit, mechanism, preclinical data, manufacturing, regulatory strategy, clinical

from: Pharmadiversityjobboard.com - 8 days ago

CyberCoders - Cambridge, MA

If you are a Manager, Data Management with Senior-level Clinical Data Management experience, please read on! Job Title: MANAGER - CLINICAL DATA MANAGEMENT Location: Cambridge, MA. Salary: $140k 140,000.00 - $180,000.00

from: cybercoders.com - 22 days ago

Clinical Dynamix, Inc. - Cambridge, MA, US

Operations. The sponsor oversight monitoring role plays a significant contribution to the clinical quality risk management strategy for the Company clinical programs. The senior manager of global monitoring

from: jobvertise.com - 30 days ago

Proclinical Staffing - Boston, MA, United States

Proclinical is seeking a dedicated Senior Clinical Trial Manager (CTM) to join our global Clinical Operations Department. The successful candidate will play a crucial role in managing and executing

from: linkedin.com - 10 days ago

Meet - Boston, MA, United States

Senior Manager/Associate Director - Clinical Data Management *Onsite 2x weekly in Boston, MA* Responsibilities: Lead data management expectations with CROs and partners Drive data management strategy

from: linkedin.com - 14 days ago

AbbVie - Waltham, Massachusetts

Responsible for the performance management of staff; supporting team in building and maintaining a high performing team, recruitment...

from: resume-library.com - 2 days ago

Stratacuity: Proven Scientific Placement - Waltham, MA, United States

Location: Waltham, MA (Hybrid) Therapeutic Area: Immuno-Oncology Job Overview: The Senior Manager/Associate Director, Biostatistics will lead statistical analyses for early development of clinical

from: linkedin.com - 19 days ago

Novo Nordisk - Lexington, MA

and optimize the way we do siRNA nonclinical development to ensure timely and adequate nonclinical regulatory documentation, safety assessments, and clinical trial support for our siRNA projects. The Senior

from: Pharmadiversityjobboard.com - 14 days ago