Sort by
Refine Your Search
-
Listed
-
Category
-
Country
-
Program
-
Field
- Medical Sciences
- Computer Science
- Economics
- Engineering
- Business
- Biology
- Science
- Mathematics
- Education
- Materials Science
- Arts and Literature
- Social Sciences
- Chemistry
- Humanities
- Environment
- Law
- Electrical Engineering
- Physics
- Linguistics
- Design
- Earth Sciences
- Psychology
- Sports and Recreation
- 13 more »
- « less
-
, medium and long-term strategic development, and signpost best practice to produce, protect and track our IP and knowledge. Possessing a degree or relevant experience in a medical or healthcare subject and
-
(Scholarly Practitioners), or IP (Instructional Practitioners). Instructor Responsibility: Temporary faculty members are responsible for adherence to and implementation of university and system-wide policies
-
) under the First-Team programme, project no. FENG.02.02-IP.05-0012/25, “EcoCool: Eco-Friendly Semiconductor Cooling Solution with Dual-Use Applications”, co-financed by the European Union under
-
August; FCT, IP Research Grant Regulation, approved by Regulation N.º 234/2012, published in the II Series of the Diário da República of June 25, 2012, amended and republished by Regulation No. 326/2013
-
tools and a catalogue of the capabilities of IDIVAL's research groups, offering them strategic support. Prepare reports on results, impact monitoring and sustainability analysis of European actions
-
, protocol submissions, and SOPs. May train others in these policies and processes. Is responsible for all aspects of managing and documenting Investigational Product (IP); including arrival, storage, tracking
-
EC2, S3, and IAM; centralized desktop and server management tools such as SCCM, Intune, JAMF. Skill configuring and maintaining an IP network including DNS and DHCP servers; Ethernet hardware and
-
dependents Exclusive staff discounts Continuous improvement and innovation Professional development through training and education A diverse and inclusive workplace And much more! As the Systems Administrator
-
assigned. Adheres to and contributes to the development of documentation standards, policies, practices, procedures and security plans. Ensures clear, concises, and timely reports are generated. Manages time
-
. Operations: Recognizes when typical agreements (MTAs, CDAs, DUAs, DTAs, etc.) are necessary and alerts appropriate parties. Prepares FDA regulatory submissions in collaboration with ORAQ, including development