Project Manager

As a Clinical Project Manager, you will be in a key position of responsibility within the Company - directly accountable to our clients and executive management team as follows: 

• Planning and delivery of Novotech's contracted responsibilities for assigned clinical projects
• Client relationship management
• Leading the internal Novotech trial project team across the US region
• Managing the project budget, scope and project revenues
   

The role is broad and varied.  The ideal candidate will have exposure to a range of trials at various phases and stages with experience managing across the US.  As a Novotech PM you will have a key role in shaping our business and reputation as a highly regarded CRO.  

You will be part of an expanding team, due to our continued success in securing new studies.  There will be ample opportunity for diligent employees to progress their career and you will be working with some of the most experienced PMs in the industry.  Our clinical professionals are immensely talented and well regarded in their field and you will be working alongside these individuals on cutting-edge therapeutic solutions.

 

Qualification & Experience:
 

• Tertiary qualifications in clinical or a life sciences related field
• Expert knowledge of the drug development process; clinical trial process, ICH GCP, local and international regulatory requirements;
• Previous project management experience in clinical trial management in a CRO environment
• Excellent interpersonal, communication and team management skills
• Possess excellent risk management and problem-solving skills
• A conscientious attitude with a can-do attitude and prepared to work in a challenging environment
• A commitment to the development of innovative treatments
• A desire to provide excellent service and focused on positive patient outcomes
• Fluent in English

 

Find out more about working at Novotech at: www.novotech-cro.com/careers

Novotech is proud to offer a great workplace. We are committed to being an employer of choice for gender equality and providing an inclusive work environment where everyone is treated fairly and with respect. 

 

Our team members are passionate about what we do, but we understand work is only of the things that is important to them. We support our team members with flexible working options, paid parental leave for both parents, flexible leave entitlements, wellness programs and ongoing development programs.

 

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.

 

We are a Circle Back Initiative Employer and commit to respond to every application. We look forward to contacting you regarding your application.

Novotech is a leading Asia-Pacific biotech specialist CRO and consists of two operating brands, Novotech and PPC. Novotech is a clinical CRO with labs, phase I facilities, and drug development consulting services.
It has accumulated experience in over 3,700 clinical projects, including Phase I to Phase IV clinical trials and bioequivalence studies. Novotech is positioned to serve biopharmaceutical clients conducting clinical trials in Asia and globally.
As of September 30, 2021, Novotech had over 2,750 FTEs across 11 geographies in Asia-Pacific, the United States and the UK.
Novotech has offices in 11 geographies across the region, and site partnerships with key medical institutions.
Novotech provides clinical development services across all clinical trial phases and therapeutic areas including: feasibility assessments; ethics committee and regulatory submissions, data management, statistical analysis, medical monitoring, safety solutions, central lab services, report write-up to ICH requirements, project and vendor management. Novotech obtained the ISO 27001 certification which is the best-known standard in the ISO family providing requirements for an Information Security Management System. Together with the ISO 9001 Quality Management system, Novotech aims at the highest IT security and quality standards for patients and biotechnology companies.