TechMojo Solutions
From TechMojo Solutions's careers page
Status: listed on the employer's own careers page when we last checked (daily). Confirm on their site before applying.
We are looking for a Clinical Project Manager to serve as the Regional Lead and the tactical owner of study execution in the assigned countries.
Each of us cares about someone who will need medicines. That’s why our vision is to repeatedly beat the odds to deliver breakthrough medicines to patients that need them. We pursue truth and scientific rigour and have the courage to work at the edge of the unknown. We are looking for a Clinical Project Manager to serve as the Regional Lead and the tactical owner of study execution in the assigned countries. You will lead a cross-functional team to deliver on our clinical trials while maximizing our clinical trial footprint across specific regional health networks and trial sites. You are a leader who can simultaneously drive global strategy at the site level and mentor your teammates as needed. H ow you might spend your days Leading cross-functional country- and regional-level study teams to ensure clinical supply and regulatory goals are aligned Developing and maintaining the Country or Regional Execution Plan(s) to ensure local site activation meets global milestones Managing the execution of clinical trials, serving as the primary liaison in the assigned countries Identifying and qualifying high-performing private research sites to diversify our profile beyond traditional academic centers Overseeing the operational implementation of protocols, ensuring site-level execution matches scientific intent Navigating the specific regional ethics landscape to ensure competitive start-up at our local sites W e’d love to hear from you if You have 8+ years of relevant hands-on experience in clinical research, in addition to a Bachelor’s degree in a related field You have 5+ years as a Project Manager leading multi-center trials and 3+ years as a CRA You have a strong understanding of ICH-GCP and TGA regulations, and bring hands-on experience managing Phase I-III clinical trials within the Australian regulatory and HREC approval landscape You have experience with advanced CTMS, eTMF, and EDC platforms, using these tools to drive data-driven decision-making You are able and willing to travel (~15%) for co-monitoring/quality control visits and territory development You are an outstanding communicator, team player, and relationship builder You continue to be inspired by working with teammates and partners to bring innovative medicines to patients, and are known for your attention to detail, timelines and creative thinking You have a passion for science, operational excellence, and innovation W hat we offer In addition to base salary and 12.5% superannuation, we offer equity and an annual bonus dependent on team and company performance. You will also have an AUD $1,500 annual Active Lifestyle Allowance, annual leave and an extended summer closure, as well as professional development opportunities. Scientific and technical mentorship is a priority. And you’ll find a strong sense of community and connections across AbCellera through our work, clubs, and socials. A bout AbCellera Creating medicines is the most important work we can do. We are a clinical-stage biotechnology company focused on discovering and developing antibody-based medicines in the areas of endocrinology, women’s health, immunology, and oncology. We have built a platform for advancing antibody drug programs from target to clinic, and we are using it to build our internal pipeline. Today, our pipeline includes two drug candidates in clinical development, two preclinical development candidates (DCs) in Investigational New Drug (IND)-enabling activities, and more than 20 active discovery programs across multiple modalities and indications. We believe that when tenacious people share a vision and work together, they can truly have a positive impact. That’s why we hire for character and intelligence, not just for CVs or experience. We look for people with drive and energy. People we trust. People who need to know their days are being well spent. That their work really matters. In the end, our success will be measured by the impact of our medicines. To apply Please submit your application through our website and refer to Job ID 23395 in your cover letter. We receive a large volume of applications and are only able to contact those who are selected for an interview. All communication from our Talent Discovery team will come from an @abcellera.com email address.
A free account lets you apply, save this job, see how well you match and check your resume against it.
Scores your resume against this job the way resume scanners do: the job's hard and soft skills, searchability, recruiter tips and formatting.
Create a free account to see your score. Your resume stays in this browser until then, and we never store it.
Already a member? Sign in