Novotech Jobs in Australia

A leading contract research organization is seeking a senior project manager specializing in early-phase clinical research projects. · Key Responsibilities: · Oversight of planning and management of early phase clinical research projects · Coordination with cross-functional teams ...

Job Description: · The Regulatory Start-Up Associate is responsible for planning, preparation, review of country and site level ethics and regulatory authority applications. · This role will be based in Australia with hybrid working arrangements (2 days in the office). · ...

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 and biostatistic ...

The Regulatory Start Up Associate is primarily responsible for planning preparation review of country and site level ethics and regulatory authority applications and submissions during project start-up. · Serve as the primary point of contact for the Regulatory Start-Up Manager ( ...

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 ...

Job Description: · Determine project feasibility, considering the needs of the sponsor · Actively provide guidance and review scope of work, responsibilities, timelines and quality of deliverables · Understand the requirements of the Project Agreement and ensure Novotech performs ...

Job Description · As a Project Manager - Early Phase Clinical Studies, you will be responsible for planning and managing contracted responsibilities for assigned early phase projects. · Duties include determining project feasibility, providing guidance on scope of work and timeli ...

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

Project management involves planning coordinating resources establishing timelines ensuring quality deliverables understanding project risks managing stakeholders supervising vendor relationships maintain records of correspondence coordination review support study clinical clinic ...

The Statistical Programmer II is primarily responsible for undertaking all statistical programming tasks on one or more clinical studies under supervision. · ...

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, · Clinical pharmacology integration. · Mentor junior consult ...

The role involves protecting trial participants' rights. · Key Responsibilities: · Ensure accuracy in trial data · ...

A leading clinical research organization is seeking a Project Manager - Early Phase. The ideal candidate will have at least 5 years of experience in clinical research along with prior project management experience. · Main Responsibilities: · ...

About the Role: · The Project Specialist is a key member of the project team and has an established professional career path for high performers. · Responsibilities include managing project deliverables, cost control, and risk management activities. · Key Responsibilities: · Assi ...

Clinical Research Project Specialist · A leading clinical research organization is seeking a specialist to support project management in clinical research studies. · Manage project deliverables and timelines · Provide overall support to the project team · ...

The Associate Clinical Data Manager (Randomization and Trial Supply Management) is responsible for planning, conducting and managing of all aspects of data management for a clinical trial according to the client specifications, protocol, project plan... · ...

Project Management in General Medicine at Novotech · About the Role · Determine project feasibility considering client needs. · Provide guidance on scope of work, responsibilities, timelines and deliverables. · We are looking for an experienced Project Manager to lead our clinica ...

Key Responsibilities: · Define a Regulatory Start Up (RSU) strategy and prepare an RSU management plan. · Oversee the execution of regulatory start up for assigned projects in accordance with the agreed RSU strategy. · ...

We are building a high-caliber drug development consulting group to partner with biotech and pharma sponsors on integrated product development plans... · ...

Senior Clinical Research Associate · This role is designed to ensure the safety and accuracy of clinical trial data. · We are seeking a Senior Clinical Research Associate (SCRA) with a degree in clinical sciences and 4+ years of relevant experience. · The ideal candidate will be ...