Clinical QA

Role & responsibilitiesShould perform sample processing smoothly as well as project execution with in assign time.Should handle instrument as well as QA observation.Should coordinate with Group members/ Group leader/ Lab managerShould be able to inspect raw data as per defined procedure.Should report inspection result properly.Should verify calibration...

QA Team Lead Summary: This Senior-level position requires extensive hands-on experience with designing, implementing and overseeing testing solutions as well as the ability to apply these concepts across various technology platforms (web-based, client-server, service oriented, legacy/mainframe, middleware components, etc.). Either the practical experience...

Role & responsibilitiesShould know to perform internal auditing.Should know to perform in-process & retrospective study audits.Should be able to perform qualification documents review.Should do SOP reviews.Should review calibration & validation documents.Preferred candidate profileExperience of 3-4 years with CRO experience only.Experience of Clinical...

Our corporate activities are growing rapidly, and we are currently seeking a full-time Software Testing Manager to join our Information Technology team in Mumbai. This position will manage a team of software testing engineers and software validation projects to implement effective and high quality software solutions. Responsibilities Lead validation staff in...

Responsible for development, implementation, maintenance, and overall success of the company's quality and regulatory programs and strategies, including articulating quality standards and objectives, developing methods to embed quality into the product development and manufacturing processes, establishing vendor relationships and quality standards, and...

Hiring Certified & Non certified Coders for multiple specialitiesDuration- 6 months of Probation with possible full-time role in futureKey ResponsibilitiesReview and abstract medical charts with precision and accuracyValidate HCC codes based on clinical documentation and coding guidelinesMaintain a daily production target of:o 120 charts for abstraction-only...

One of our client based at Mumbai (Reputed MNC Company) is looking for below positionsRole & responsibilities1. Asst Manager / Manager/Sr. Manager - Biologics Regulatory Affairs (Clinical Trials)-2 positionsJob Location: Govandi (East ), Mumbai (alternate Saturday working)Desired Qualification: M.Pharm/B.PharmDesired Work Experience: 5-10 yearsJob...

Qualification - MBBS with MD/DNB-RadiologyExperience - 2-5 yearsFemale PreferredHe / She will direct day to day functioning of the Department in accordance with the current standards, regulations and best practice guidelines.He / She will directly supervise the clinical care of patients coming to Department and ensuring their proper disposal.He /She will...

Contract: Permanent Full-TimeClosing Date: 05/12/25We are seeking Senior Regulatory Submissions Managers to play a pivotal role in shaping how regulatory submissions are managed within our new Veeva RIMS platform.This is a high-impact opportunity to influence process design, system configuration, and regulatory compliance across a global organization.The...

Job Overview:Manages the document classification under Smart Inbox and ARC review (as applicable) as well as document deletion.Summary of Responsibilities:•Maintains an understanding of applicable regulatory requirements.•Managing electronic Trial Master Files (eTMF), (Trial, Country, and Site artifacts) for clinical studies in accordance with TMF...