) – Data Management plans and implements the capture, cleaning and storage of all Amgen clinical study and trial management... experience Or Associate's degree and 8 years of clinical experience Or High school diploma/GED and 10 years of clinical...
The Senior Clinical Research Associate will play a key role in proactively helping the conduct of pre-market and post...Title: Sr. Clinical Research Associate Location: Sunnyvale, CA Duration: 12+ Months Client...
The Senior Clinical Research Associate will play a key role in proactively helping the conduct of pre-market and post...Description: Sr. Clinical Research Associate Purposeful Onsite Sunnyvale, CA Billrate - BR - BR Company...
The Senior Clinical Research Associate will play a key role in proactively helping the conduct of pre-market and post... will be required to work closely with clinical study managers, clinical trial assistants (CTAs) and data management for the conduct...
mollis, est non commodo luctus, nisi erat porttitor ligula. Clinical Research Associate - Oncology - West Location...__ ICON Strategic Solutions * __vacancyopjusttionswidget.opt-Remote Working __ Remote Senior Talent Acquisition Business...
. Job Description Are you looking for a patient-focused, innovation-driven company that will inspire you and empower you to shine? Join us as an Associate Medical... strategy for the overall global clinical development of assigned Takeda pipeline compound(s) taking into consideration the...
POSITION OBJECTIVES: The Associate Medical Director leads and drives strategy for the overall global clinical development... decision making to clinical development issues. This individual interacts with and influences R&D senior leadership decision...
(such as Trial Master File (TMF), Clinical Protocols and Reports). May interact with RA/QA in responding to audits and FDA inquiries... experience of the clinical trial process including study design and conduct; clinical data management systems; clinical trial...
(such as Trial Master File (TMF), Clinical Protocols and Reports). May interact with RA/QA in responding to audits and FDA inquiries.... Solid understanding and demonstrated experience of the clinical trial process including study design and conduct; clinical...
and activities required for and related to clinical trial initiation, maintenance and completion Strong verbal and written... program-specific late development biomarker/translational plans, responsible for aiding in creation of clinical protocols...
. Conducts daily work and clinical trial activity in accordance with Good Clinical Practice Guidelines. Adapts behavior to the... today! This job evaluates, initiates, and maintains activities related to the conduct of clinical trials with the assistance and guidance...
of clinical trial data throughout the full lifecycle of multiple clinical trials according to the Code of Federal Regulations... device accountability and reconciliation. Assist senior staff in development of study-specific forms and trial-specific...
(such as Trial Master File (TMF), Clinical Protocols and Reports). May interact with RA/QA in responding to audits and FDA inquiries... rapport with team members, peers, and management. Solid understanding and demonstrated experience of the clinical trial...
on , , , , and . Job Description The Senior Manager, Clinical Data and Reporting Standards (CDARS) proactively participates in the development of data... and reporting standards in support of AbbVie’s portfolio of clinical trials and ensures AbbVie’s conformance to CDISC standards...
on , , , , and . Job Description The Senior Manager, Clinical Data and Reporting Standards (CDARS) proactively participates in the development of data... and reporting standards in support of AbbVie's portfolio of clinical trials and ensures AbbVie's conformance to CDISC standards...
Position: Senior Manager/Associate Director, Regulatory Affairs (EDG-2025026) Location: Boston, MA Job Id: 186... # of Openings: 1 Senior Manager/Associate Director, Regulatory Affairs About Edgewise Therapeutics: At Edgewise...
clinical trial in coordination with other care providers. To perform this job successfully, an individual must be able..., & oversight of investigational drug administration schedule and conducts daily work and clinical trial activity in accordance...
, and confirms eligibility of subject to participate in clinical trial Perform informed consent process or ensures that the informed... studies through phone contacts and personal interviews Schedule subject participation in research clinical trial...
. As the Senior Global Program Clinical Head (GPCH), you are the clinical lead and will serve as a key member of the Global... in program(s). Lead a cross functional team through the creation of clinical components of key documents (e.g., Clinical Trial...
of clinical trial sites across the drug development lifecycle. We offer integrated strategic/operational consulting... clinical trial budget documents. Perform prospective reimbursement (coverage) analysis according to CMS National Coverage...