ICH Jobs in USA

We are seeking a Senior Quality Control Specialist/ Auditor to support the implementation of M3 Wake Research quality initiatives. In this role you will conduct audits to ensure our operations comply with Standard Operating Procedures (SOPs) local and federal regulations ICHGCP guidel More...

We are seeking a Senior Quality Control Specialist/ Auditor to support the implementation of M3 Wake Research quality initiatives. In this role you will conduct audits to ensure our operations comply with Standard Operating Procedures (SOPs) local and federal regulations ICHGCP guidel More...

Job Title: Quality Engineer Stability Program (Temporary) Job Location: Saint Louis MO Job Type: Contract (6months with chance of converting to fulltime) Summary: We are looking for a temporary Quality Engineer focused on supporting the Stability Program. This role ensures the pro More...

Job Title Process Monitoring and Data Analytics Location Parsippany NJ Hybrid Onsite T/W/Th Working hours: 84:30 8:305 95:30 type of hours (most of team works 95) Responsibilities: Process Engineer/Validation Engineer having strong background in statistics process monitori More...

Our client is a leading biopharmaceutical company dedicated to developing therapies to better their patients lives and driven by an entrepreneurial mindset and a teamoriented culture. Position Overview The Vice President of Regulatory will oversee all aspects of Regulatory operations. More...

Medical guidance to site personnel and the project team regarding Protocol and other studyspecific medical aspects 24/7 medical consultancy support to investigators and project team Monitoring of patients safety and wellbeing:o Detection of trends and outlierso Signal detectiono Elig More...

Summary:The Clinical Program Director is a fulltime role responsible for overseeing clinical operations program development and mental health initiatives. This position ensures highquality patient care and treatment outcomes through leadership and collaboration with medical staff.Resp More...

Specjalista/Manager ds. Rozwoju Biznesu (brana spoywcza)Firma specjalizujca si w produkcji i dystrybucji wysokiej jakoci dodatkw spoywczych aromatw oraz ekstraktw. czy nowoczesne technologie z zaawansowan wiedz w zakresie chemii i technologii ywnoci dostarczajc rozwizania dopasowane d More...

About the Role: The Senior Director of Clinical Development will be instrumental in advancing clinical research strategies for obesity and liver disease candidates. This individual will ensure all programs meet stringent safety and quality standards required by the medical community a More...

About the Role: The Senior Director of Clinical Development will be instrumental in advancing clinical research strategies for obesity and liver disease candidates. This individual will ensure all programs meet stringent safety and quality standards required by the medical community a More...

DIRECTOR/SENIOR DIRECTOR OF REGULATORY CHEMISTRY MANUFACTURING AND CONTROLS (CMC)Company Overview:Mythic Therapeutics is a privately held clinical stage productplatform company building a pipeline of bestinclass antibody drug conjugates (ADCs) exhibiting a combination of unprecedented More...

Hi Hope all is well Please revert me with your updated profile if you like this JD to apply Quality Systems Specialist Hybrid role in Waltham MA ( Local only) Duration 5 months (with extension possible) Must Have vs. Plus 23 years exp. In biotech or regulated industry (require More...

The Clinical Trial Rater a mental health professional will be solely responsible for interviewing research participants and their informants/caregivers who are being evaluated to participate in a research study for various cognitive and behavior disorders.Including but not limited to More...

SummaryThe Director of Clinical Operations will leverage a strong scientific background and leadership expertise to advance programs from firstinhuman studies to laterstage development. This individual will integrate scientific clinical and business considerations into cohesive study More...

The Clinical Trial Rater a mental health professional will be solely responsible for interviewing research participants and their informants/caregivers who are being evaluated to participate in a research study for various cognitive and behavior disorders.Including but not limited to More...

In this role you will work with the Clinical Data team to interpret and organize clinical oncology data. Reporting to the Clinical Data Manager you will develop realworld data variables from structured and unstructured sources design data capture forms and establish procedures for dat More...

The Clinical Trial Rater a mental health professional will be solely responsible for interviewing research participants and their informants/caregivers who are being evaluated to participate in a research study for various cognitive and behavior disorders.Including but not limited to More...

The Clinical Trial Rater a mental health professional will be solely responsible for interviewing research participants and their informants/caregivers who are being evaluated to participate in a research study for various cognitive and behavior disorders.Including but not limited to More...

The Clinical Trial Rater a mental health professional will be solely responsible for interviewing research participants and their informants/caregivers who are being evaluated to participate in a research study for various cognitive and behavior disorders.Including but not limited to More...

The Clinical Trial Associate supports the clinical operations project team to ensure the smooth execution of clinical trial processes in compliance with regulatory guidelines and ICH/GCP standards. This role involves managing trial documents coordinating project activities and assisti More...