Clinical Regulatory Affairs Jobs
ClinCrowd - Waltham, MA, United States
Extensive knowledge of non-clinical and clinical development, regulatory guidelines of FDA, ICH, EMA, EU NCAs, MHRA and other international...
from: linkedin.com - 5 days ago
Stratacuity: Proven Scientific Placement - Waltham, MA, United States
Job Overview: This role involves developing regulatory strategies, leading interactions with regulatory authorities, overseeing regulatory...
from: linkedin.com - 4 days ago
SystImmune - Redmond, WA, United States
with cross-functional teams, including research, clinical development, biostatistics, and regulatory affairs, to define biomarker strategies and integrate companion diagnostics into clinical trial protocols
from: linkedin.com - 4 days ago
SystImmune - Redmond, WA, United States
, clinical development, biostatistics, and regulatory affairs, to define biomarker strategies and integrate companion diagnostics into clinical trial protocols. Generate technical documentation, including
from: linkedin.com - 4 days ago
Eclaro - Lawrence, NJ, United States
communications to additional documents and activities such as: Dear Health Care Professional letters, Clinical Overview for Type II variation, Periodic Benefit-Risk Evaluation regulatory document submissions
from: linkedin.com - 5 days ago
Medix™ - Deland, FL, United States (+1 location)
and industry standards. Lead the screening of eligible participants for clinical trials. Collaborate with cross-functional teams, including research coordinators, data managers, and regulatory affairs, to ensure
from: linkedin.com - 10 days ago
HonorHealth - Scottsdale, AZ, United States
, patient engagement and regulatory affairs Execute research protocols according to FDA regulations and GCP guidelines Evaluate patient’s eligibility for clinical trials Adhere to industry standards
from: linkedin.com - 12 days ago
GForce Life Sciences - , CA, United States
are harmonized and ensure delivery of high-quality data and analysis results for regulatory submissions Lead discussions and interacts with members of the Data Management and Clinical Affairs teams to align
from: linkedin.com - 11 days ago
GAP Solutions, Inc. - Bethesda, MD, United States
site monitoring, regulatory compliance, protocol development, clinical research, clinical trials, and protocol writing. Experienced in data monitoring, data integrity, patient care, recruitment
from: linkedin.com - 13 days ago
Kelly Science, Engineering, Technology & Telecom - Irvine, CA, United States
Regulatory Affairs Specialist (hybrid) Kelly Science and Clinical FSP is currently seeking a medical device Regulatory Affairs Specialist II for a long-term engagement in Irvine, CA
from: linkedin.com - Yesterday
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