Novotech Jobs in Australia

About the Role · The Project Manager - Early Phase is primarily responsible for the planning and management of all contracted responsibilities for assigned early phase projects and to act as the primary contact between Novotech and its clients. · Based anywhere in AU · Responsibi ...

The Senior Clinical Research Associate (SCRA) is primarily responsible for ensuring the rights and wellbeing of trial participants are protected and the reported trial data are accurate complete and verifiable from the source documents. · This role would suit a SCRA who has had e ...

Job Title: Project Manager Early Phase Clinical Trials · About the Role: · The Project Manager - Early Phase is primarily responsible for planning and managing all contracted responsibilities for assigned early phase projects. · Determine project feasibility, considering the need ...

Description · The Clinical Research Associate (CRAII - CRAIII), is primarily responsible for ensuring the rights and wellbeing of trial participants are protected and the reported trial data are accurate, complete, and verifiable from the source documents. The CRA is the primary ...

Description · About the Role · The Project Manager – Early Phase is primarily responsible for the planning and management of all contracted responsibilities for assigned early phase projects and to act as the primary contact between Novotech and its clients. · Responsibilities · ...

Associate Clinical Data Manager · About the Role: · The Associate Clinical Data Manager is responsible for planning, conducting and managing all aspects of data management for a clinical trial according to client specifications. · This role involves developing Trial Supply Manage ...

The Senior Clinical Research Associate (SCRA) is primarily responsible for ensuring the rights and wellbeing of trial participants are protected and the reported trial data are accurate, · complete,and verifiable from the source documents.This single sponsor (FSP) role will be ba ...

The Project Specialist assists PMs in managing project deliverables. · We are looking for people who are passionate about working clinical research and biotech, · including people who identify as LGBTIQ+, have a disability or have caring responsibilities.Assist the PMs to manage ...

Regulatory Start-Up Specialist — Australia · A leading clinical research organization in Australia is seeking a Regulatory Start Up Associate to manage the planning and preparation of regulatory applications. The ideal candidate will have a background in clinical, pharmacy, or li ...

Description · The Clinical Research Associate (CRAII - CRAIII), is primarily responsible for ensuring the rights and wellbeing of trial participants are protected and the reported trial data are accurate, complete, and verifiable from the source documents. The CRA is the primary ...

The Clinical Research Associate (CRAII - SCRA) is responsible for ensuring the rights and wellbeing of trial participants are protected. · ...

The Regulatory Start Up Associate is primarily responsible for planning, preparation and review of country and site level ethics and regulatory authority applications and submissions during project start-up. · ...

We are building a high‑caliber drug development consulting group to partner with biotech and pharma sponsors on integrated product development plans, · global regulatory strategy, · clinical protocol and development design, · CMC, · clinical pharmacology, · nonclinical strategy, ...

About the Role · The Project Manager - General Medicine is primarily responsible for the planning and management of all contracted responsibilities for assigned projects and to act as the primary contact between Novotech and its clients. This role requires previous CRO experience ...

The Project Manager - Early Phase is primarily responsible for the planning and management of all contracted responsibilities for assigned early phase projects. · ...

The Regulatory Start Up Associate is primarily responsible for planning, preparation and review of country and site level ethics and regulatory authority applications and submissions during project start-up, · in compliance with ICH-GCP local regulatory requirements to ensure tim ...

The Clinical Research Associate (CRAII - CRAIII), is primarily responsible for ensuring the rights and wellbeing of trial participants are protected and the reported trial data are accurate, complete, and verifiable from the source documents. The CRA is the primary contact betwee ...

About the Project Manager Role · The primary responsibility is to plan and manage contracted responsibilities for assigned projects, acting as the main point of contact between Novotech and clients. This role requires previous CRO experience, ideally in cell therapy. · Key Respon ...

A key role in our Novotech clinical research organization is the Regulatory Start-Up Specialist, Clinical Trials. This position involves overseeing ethics and regulatory submissions during project initiation. · Key responsibilities of this job include ensuring compliance with all ...

The Clinical Research Associate (CRAII - CRAIII), is primarily responsible for ensuring the rights and wellbeing of trial participants are protected and the reported trial data are accurate, complete, and verifiable from the source documents. The CRA is the primary contact betwee ...