BeiGene
Employer Industry: Biotechnology and Pharmaceutical Research
Why consider this job opportunity
Salary up to $97,800 annually
Eligibility for an annual bonus plan for non-commercial roles and an incentive compensation plan for commercial roles
Comprehensive benefits package including Medical, Dental, Vision, 401(k), FSA/HSA, Life Insurance, Paid Time Off, and Wellness programs
Opportunity to own shares of the employer's stock through discretionary equity awards and participation in the Employee Stock Purchase Plan
Work in a collaborative and innovative environment focused on fighting cancer
Chance to contribute to the improvement of clinical trial processes and infrastructure across the Americas
What to Expect (Job Responsibilities)
Support the delivery of study start-up and ongoing submissions within established timelines and quality standards
Drive the kick-off and completion of tasks from selection through activation of clinical sites
Manage document preparation and submission to central IRB for timely reviews
Assist in the collection and review of essential documents while maintaining CTMS data entry
Contribute to the development of local workflows to streamline output and enhance deliverables
What is Required (Qualifications)
Bachelor’s degree or higher in a scientific or healthcare discipline preferred
Minimum of 3 years of progressive experience in clinical research and clinical operations
Knowledge of ICH/GCP and relevant country regulations/guidelines
Strong written and verbal communication skills
Highly organized with the ability to prioritize tasks effectively
How to Stand Out (Preferred Qualifications)
Experience in the biotech, pharmaceutical sector, CRO, or clinical site environment
Diligence in follow-through and ability to work collaboratively in a team setting
Demonstrated initiative and an entrepreneurial mindset
Familiarity with Microsoft Office applications, including Outlook, Word, Excel, PowerPoint, and Teams
We prioritize candidate privacy and champion equal-opportunity employment. Central to our mission is our partnership with companies that share this commitment. We aim to foster a fair, transparent, and secure hiring environment for all. If you encounter any employer not adhering to these principles, please bring it to our attention immediately. We are not the EOR (Employer of Record) for this position. Our role in this specific opportunity is to connect outstanding candidates with a top-tier employer.
#J-18808-Ljbffr
Why consider this job opportunity
Salary up to $97,800 annually
Eligibility for an annual bonus plan for non-commercial roles and an incentive compensation plan for commercial roles
Comprehensive benefits package including Medical, Dental, Vision, 401(k), FSA/HSA, Life Insurance, Paid Time Off, and Wellness programs
Opportunity to own shares of the employer's stock through discretionary equity awards and participation in the Employee Stock Purchase Plan
Work in a collaborative and innovative environment focused on fighting cancer
Chance to contribute to the improvement of clinical trial processes and infrastructure across the Americas
What to Expect (Job Responsibilities)
Support the delivery of study start-up and ongoing submissions within established timelines and quality standards
Drive the kick-off and completion of tasks from selection through activation of clinical sites
Manage document preparation and submission to central IRB for timely reviews
Assist in the collection and review of essential documents while maintaining CTMS data entry
Contribute to the development of local workflows to streamline output and enhance deliverables
What is Required (Qualifications)
Bachelor’s degree or higher in a scientific or healthcare discipline preferred
Minimum of 3 years of progressive experience in clinical research and clinical operations
Knowledge of ICH/GCP and relevant country regulations/guidelines
Strong written and verbal communication skills
Highly organized with the ability to prioritize tasks effectively
How to Stand Out (Preferred Qualifications)
Experience in the biotech, pharmaceutical sector, CRO, or clinical site environment
Diligence in follow-through and ability to work collaboratively in a team setting
Demonstrated initiative and an entrepreneurial mindset
Familiarity with Microsoft Office applications, including Outlook, Word, Excel, PowerPoint, and Teams
We prioritize candidate privacy and champion equal-opportunity employment. Central to our mission is our partnership with companies that share this commitment. We aim to foster a fair, transparent, and secure hiring environment for all. If you encounter any employer not adhering to these principles, please bring it to our attention immediately. We are not the EOR (Employer of Record) for this position. Our role in this specific opportunity is to connect outstanding candidates with a top-tier employer.
#J-18808-Ljbffr