...The Opportunity
Description
We're looking for a Clinical Data and Documentation Coordinator , working in Pharmaceuticals and Medical... ...Cambridge, Massachusetts, United States .
Works closely with Manager and Clinical Operations personnel to perform quality...
Suggested
...Rose International
Position Number: 464270
Job Title: QA Documentation Specialist
Job Location: Newton, MA, USA, 02466
Work... ...).
• Ensuring that all changes and associated documents are managed in accordance with internal and external standards, policies,...
Suggested
Hourly pay
Temporary work
Shift work
...Job Description
Manager, Global Clinical Supply Management
This is what you will do:
The Manager, Clinical Supply plans, establishes... ...contract providers.
Manage Quality Systems required documentation, including on-time open and close of Deviations,...
Suggested
Contract work
For contractors
Document Processing needs no experience
Document Processing requires:
Interview times M-F 4-5p
Ability to lift up to 20-40 pounds... ...set by the Clients.
Ability to sit and or stand for long periods of time.
Perform other tasks as needed assigned by management
Suggested
...The Opportunity:
As Clinical Project Manager, you will be accountable for managing clinical studies that will lead the biopharma industry... ...program teams.
* You will contribute to or author key study documents including, but not limited to, protocols, informed consent...
Suggested
...meticulous and detail-oriented Engineering Documentation Specialist to join our team. The ideal... ...What will you do?
Change Control Management: Utilize Oracle for initiation of... ...are supported by real science, robust clinical evidence, and an unrelenting focus on patients...
Suggested
Work experience placement
Local area
...Description
Job Description Position Summary:
The Director Trial Master File (TMF) and Clinical Documentation spearheads the vision and strategy for records management of clinical trial documents. They are accountable for leadership of the TMF organization, including...
Suggested
Local area
Flexible hours
...product candidates from our platform into clinical studies, including vimseltinib and DCC-3... ...best practices including risk-based management
Work closely with GCP/GLP/GVP functional... ...management files and other relevant documents as needed
Escalate issues of critical...
Suggested
Contract work
Temporary work
For contractors
Summer work
Summer holiday
Flexible hours
...their personal and professional ambitions.
The Senior Clinical Trials Manager/Clinical Trials Manager (CTM) is responsible for leading the... ...study drug distribution and accountability processes and documentation
* Oversight of study start-up, study management, data cleaning...
Suggested
Holiday work
Temporary work
Local area
Immediate start
Remote job
...respect, diversity, teamwork, excellence and innovation in their work activities and interactions.
Among other tasks the clinical pharmacy manager:
- Promotes staff's clinical development
- Guides clinical pharmacists' interventions with other health professional...
Suggested
Day shift
Weekday work
POSITION SUMMARY:
TScan Therapeutics is a clinical-stage biotech seeking to revolutionize... ...are looking for a Senior Clinical Data Manager to oversee data management activities across... ...edit checks
~Develop data management documents to support study execution (e.g. Data...
Suggested
Flexible hours
...lead with the desire to work on novel ideas. As a Director Clinical Data Management, this individual will report to the Senior Director... ...data management policies, SOPs, processes, clinical systems, documents, and other tools.
What you'll do
Serve as data management...
Suggested
Holiday work
Temporary work
Immediate start
...Description
We're looking for a QA Document Coordinator , working in... ...Client
Our client is an award-winning clinical development company. Improving lives globally... ...and administrative experience
Project management skills
Ability to work independently...
Suggested
Shift work
...Sr. Clinical Trial Manager 2019622 Location: Waltham, MA (Hybrid) Therapeutic Area: Auto Immune Job Overview: We are looking for a talented... ...and external stakeholders
Operational input into study documents such as synopsis, protocol, Informed Consent, CRFs, CRF Completion...
Suggested
...Position: LTSS - Clinical Care Manager
Department: BAP Program
Schedule: Full Time
POSITION SUMMARY:
The LTSS Clinical Care... ...visits with selected Enrollees as appropriate.
Completes documentation in the medical management information system in a timely...
Suggested
Full time
Temporary work
Work experience placement
Remote job
Work from home
Home office
...Chief Pharmacy Officer and Associate Chief Pharmacy Officer, Clinical Pharmacist Manager supports mission and goal achievement, organizational... ...matter expert buy in to improve direct patient care.
• Documents pharmacist interventions and reviews collated reports periodically...
Local area
Shift work
...oversight, coordination, and execution of clinical trials in support of clinical programs... ...with the Sr. CTM and/or Clinical Program Manager and is responsible for oversight,... ...participates in development of clinical study documents including ICF, monitoring plans, recruitment...
Contract work
Flexible hours
3 days per week
...urgent care, so we're there for pets when they need us most. Our clinics are designed with pets and people in mind: warm, friendly, and... ...up - and we're looking for a collaborative Veterinary Clinic Manager to join our team.
Our Veterinary Clinic Manager will lead our...
Full time
Local area
Immediate start
...Job Posting Description
The Hematology Clinical Research Group at the Dana-Farber/Boston... ...Center is seeking a clinical research manager. Ground-breaking research within the group... ...Assumes responsibility for essential document compliance for entire portfolio. Implements...
Work experience placement
...Overview
Responsible for aspects of clinical development planning and strategy, clinical... ...study related materials, relationship management between study sites and vendors (in particular... ...use, enrollment of subjects, regulatory document flow, study timelines, all budgetary and...
