About the Role The Associate Director Information Technology will be responsible for the global service delivery framework. Collaborate and engage service delivery from other functions to develop a cohesive and consistent ESM framework. Collaborates with and seeks
The Regulatory Start-Up Associate II (RSA) are responsible for the planning, preparation, and review of country- and site-level ethics and regulatory authority submissions during the start-up phase of clinical trials, and, where applicable, throughout maintenance and close-out.
Passionate about biotech? So are we. At Novotech, youll work with innovative biotech and pharmaceutical sponsors who are deeply invested in their science and passionate about their molecules. As we continue to grow across Early Clinical Development and
The Inhouse Clinical Research Associate (IHCRA) provides in-house support to the clinical team according to project requirements, ICH GCP guidelines, local or global regulatory requirements and Novotech or Client SOPs. Responsibilities: Support the clinical team’s inhouse activities
The Regulatory Start-Up Associate (RSA) and Regulatory Start-Up Lead (RSL) are responsible for the planning, preparation, and review of country- and site-level ethics and regulatory authority submissions during the start-up phase of clinical trials, and, where applicable,
About us BeOne is a global oncology company that is discovering and developing innovative treatments that are more affordable and accessible to cancer patients worldwide. With a broad portfolio, we are expediting development of our diverse
The Clinical Research Associate (CRA), 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
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to
About the role The Project Manager is primarily responsible for the planning and management of all contracted responsibilities for assigned projects. Act as primary contact between Novotech and client. Leads and oversees the execution of clinical
About the role The Project Manager is primarily responsible for the planning and management of all contracted responsibilities for assigned projects. Act as primary contact between Novotech and client. Leads and oversees the execution of clinical
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Join Us as an Assistant Clinical Research Associate – Make an Impact at the Forefront of Innovation! At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact
The Role: Joining Moderna offers the unique opportunity to be part of a pioneering team thats revolutionizing medicine through mRNA technology, with a diverse pipeline of development programs across various diseases. As an employee, youll be
The Clinical Lead/associate Clinical Lead provides direction and guidance to the project team, coordinate site management and monitoring activities, and communicating status of these activities to the PM. Regional Clinical Lead responsibilities may include, but are not
Patent Attorney -Chemical/Chemistry (Associate-Senior Associate) Surpass your own ‘limits’ Empowering Career. Unbeatable mentors. Enviable clients. Exciting growth opps. Life friendly/part WFH. Premier IP firm. $90,000-$200,000+ Generous bonus $. SYDNEY/MELBOURNE OR BRISBANE. YOUR NEW EMPLOYER Our client is an
Patent Attorney (Life Sciences/Bio Tech/Bio Chemistry/Biology) DARE TO SOAR to YOUR MAX Empowering+ Enviable Career. Elite multi-award winning firm. LIFE +Play+ flexibility+ $+generous BONUS+PERKS. SYDNEY. THE FIRM Our client is an internationally renowned multi-award winning elite
At Australian Biotechnologies, we’re proud to be Australia’s leading manufacturer of allograft implants, honouring the gift of donation and improving the wellbeing of patients nationwide. Our products support a wide range of surgical procedures, helping clinicians
Parkville/hybrid opportunity | Close to public transport Full or part time 2-year contract | 0.8-1.0 considered Supportive on the job development | Join a passionate team About Orygen Orygen is Australia’s Centre of Excellence in
Vendor Management Manager: The Vendor Management Manager will act as the primary point of contact for Novotech for project-related vendor management across the company. Establish and maintain vendor database, including vendor CDAs/MSAs. Communicate with project teams
The Regulatory Start-Up Associate (RSA) and Regulatory Start-Up Lead (RSL) are responsible for the planning, preparation, and review of country- and site-level ethics and regulatory authority submissions during the start-up phase of clinical trials, and, where applicable,
About the Role The Associate Director, IT Compliance is responsible for organising, leading and continuously improving Novotech’s IT Compliance function across a global CRO environment. The role provides leadership for IT governance, compliance assurance, audit readiness, vendor