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Senior Trial Manager/Trial Lead

Accountable for all operational aspects of assigned clinical trial.s. executed by GBS Clinical Trial Services on behalf of Novartis Organizations. ......Clinical......tocol generation to clinical...... for the writing of clinical...... View more..

Clin Ops Quality Specialist-

PurposeConduct on site risk assessment visits with CRAs to investigate risks associated with the conduct of clinical trials and the ......e-identified by the Clinical...... Operations Quality Manager......it whenrequested by Clinical...... View more..

Technical Specialist UP TSU project

Develop liaison with State health officials, and District health officials to strengthen Family Planning training centers and develop new District ......e complete range of clinical......clinical......rdization exercises clinical...... View more..

Lead-Clinical Data Manager- SR

Job Description:- Ensure quality and timely clinical data delivery for multiple CPO local studies and projects outsourced to international Contract ......rance review of key clinical......rve as Project Data Manager......Management input to Clinical...... View more..

Senior Medical Writer

Job Description :The Senior Medical Writer researches, creates, and edits all documents associated with clinical research. Responsibilities also include: acting ......countabilitiesWrite clinical......briefing documents, clinical......, interim and final clinical...... View more..

Senior Medical Writer

Job Description :The Senior Medical Writer researches, creates, and edits all documents associated with clinical research. Responsibilities also include: acting ......countabilitiesWrite clinical......briefing documents, clinical......, interim and final clinical...... View more..

Senior Medical Writer

The Senior Medical Writer researches, creates, and edits all documents associated with clinical research. Responsibilities also include: acting as primary ......countabilitiesWrite clinical......briefing documents, clinical......, interim and final clinical...... View more..

Clin Ops Quality Specialist

RESPONSIBILITIES As a monitor, undertake normal activities as described by the Senior CRA job description with additional training in riskmanagement, ......it whenrequested by Clinical...... Operations Quality Manager...... recommendations to Clinical...... View more..

Sr Clin Process Specialist

Apply clinical research expertise to provide project related assistance across complex and multiple project.s., sites and project teams. Lead teams ......and practices, good clinical......rics. Mentor/ coach Clinical......holders and/or line manager...... View more..

Senior Medical Writer

Job DescriptionThe Senior Medical Writer researches, creates, and edits all documents associated with clinical research. Responsibilities also include: acting as ......countabilitiesWrite clinical......briefing documents, clinical......, interim and final clinical...... View more..

Senior Medical Writer

Job Description :The Senior Medical Writer researches, creates, and edits all documents associated with clinical research. Responsibilities also include: acting ......countabilitiesWrite clinical......briefing documents, clinical......, interim and final clinical...... View more..

Senior Medical WriterApply

Job Description :The Senior Medical Writer researches, creates, and edits all documents associated with clinical research. Responsibilities also include: acting ......countabilitiesWrite clinical......briefing documents, clinical......, interim and final clinical...... View more..

Clinical Trial Assistant (CTA)

JOB FUNCTIONS/RESPONSIBILITIES: To provide general administrative support to the Clinical Operations Department and assistance to Project Manager.s. and Project Director.s.. ......Clinical......ls. To support the Clinical......th the roles of the Clinical...... View more..

Clinical Research Assoicate

Description:Ensure that clinical studies within Centralized Clinical Operations are conducted in accordance with the protocol, standard operating procedures, Good Clinical ......ompliance with Good Clinical......lity issues to Lead Clinical......lyst, Site Monitor, Clinical...... View more..

Senior Medical Writer

Key AccountabilitiesWrite clinical documents for submission to regulatory authorities, including but not limited to: briefing documents, clinical development plans, previous ......, interim and final clinical......ical document .CTD. clinical......capacity of project manager...... View more..

Sr Clinical Trial Assistant

Description- Completes appropriate protocol and fundamental clinical research training including the requirements of GCPs/ICH guidelines and applicable local regulations. - ......g multiple types of clinical......ement.- Assists the clinical......iling, archiving of clinical...... View more..

CRA III

A brief summary of duties you will be involved in as a CRA:1. Communication - Maintains timely and effective communication ......nitors all types of clinical...... Forms according to Clinical......onitoring. Performs clinical...... View more..

Sr Clinical Trial Assistant

Description- Completes appropriate protocol and fundamental clinical research training including the requirements of GCPs/ICH guidelines and applicable local regulations. - ......g multiple types of clinical......ement.- Assists the clinical......iling, archiving of clinical...... View more..

Sr Clinical Trial Assistant

Completes appropriate protocol and fundamental clinical research training including the requirements of GCPs/ICH guidelines and applicable local regulations.- Assists CTL ......g multiple types of clinical......ment. - Assists the clinical......iling, archiving of clinical...... View more..