Bristol Myers Squibb Senior Clinical Trial Monitor in Victoria, Australia
At Bristol Myers Squibb, we are inspired by a single vision – transforming patients’ lives through science. In oncology, hematology, immunology and cardiovascular disease – and one of the most diverse and promising pipelines in the industry – each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference.
Senior Clinical Trial Monitor
BMS is seeking an experienced and energised clinical research professional with strong communication and relationship building skills to oversee the progress & conduct of clinical trials. This is a great opportunity to join highly energetic and supportive environment within a clinical operations team globally recognised for its excellence in delivering transformational medicines for patients in multiple therapeutic areas
BMS is Australia's fastest growing pharmaceutical company with a rapidly expanding suite of innovative therapies and indications. We're committed to improving patient outcomes and the Senior Clinical Trial Monitor will perform a vital role in driving drug access for patients.
Collaborating with internal and external stakeholders to identify new potential investigators & assesses suitability
Recommending sites during site feasibility and/or site selection processes
Conducting pre-study and site initiation visits – setting up vendors during study start up period
Setting up vendors during study start up period
Developing and maintaining site relationships to serve as the primary point of contact & training support
Proactively identifying and resolving potential problems across all levels
Engaging with colleagues to assist in the resolution of more complex issues
Coaching to enhance the performance of the broader team
Serving as a key resource to colleagues by providing guidance, leading training and acting as a mentor
Reviewing site activities and quality whilst conducting monitoring activities following the plan, procedure, protocol, guidelines and local regulations
Performing unblinded site Monitor activities to protect the blind of the study
Managing multiple protocols across multiple therapeutic areas
Ensuring completeness and quality of data and its availability and currency
Motivating and influencing sites to meet study objectives with a flexible communication style
Anticipating, identifying and proactively supporting the resolution of issues that arise, & escalating as appropriate
Preparation and submission of written reports
Essential Skills & Qualifications:
Strong administration background with organisation and time management skills
Experience in Clinical Trial Monitoring with demonstrable leadership, mentoring and coaching capability
General knowledge of software systems and web-based applications with a willingness to learn
Basic knowledge of the clinical research process is ideal, as well as budgeting and finance management
Tertiary qualifications (or equivalent) in a health / biological sciences or administration related field
Around the world, we are passionate about making an impact on the lives of patients with serious diseases. Empowered to apply our individual talents and diverse perspectives in an inclusive culture, our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.
Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives.
Company: Bristol Myers Squibb
Req Number: R1540955
Updated: 2021-06-23 02:53:25.392 UTC
Bristol Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, pregnancy, citizenship, marital status, gender expression, genetic information, political affiliation, or any other characteristic protected by law.
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