Role Description
The Associate CRM oversees clinical monitoring activities and the CRA team's performance to ensure they comply with ICH-GCP, local regulations, and company SOPs, and maintain quality across clinical trials. As a line manager, this role leads a team to achieve organizational goals and ensure high performance by providing guidance, support, and development opportunities while promoting a positive team culture.
Essential Functions of the Job
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Team Resource Allocation & Performance:
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Allocate CRA resources and perform ongoing resource assessments to ensure a balanced workload for quality monitoring and to meet study deliverables.
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Ensure CRAs have the required level of monitoring knowledge and skills to successfully perform required activities with high quality to meet study deliverables.
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Manage and address CRA performance and quality indicators in accordance with ICH-GCP, SOPs, and local regulations.
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Strengthen site relationships to enhance performance and uphold the company’s trial delivery reputation.
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Quality and Compliance:
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Review monitoring quality and resolve issues to ensure compliance with regulatory guidelines, ICH-GCP Guidelines, and Good Clinical Practices.
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Support study/site milestone delivery in collaboration with cross-functional teams.
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Responsible for execution of assessment visits and accompanied visits (where required) to assess ongoing CRA monitoring competency, identifying issues and developing resolution strategies.
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Contribute to process optimization initiatives and manage risk escalation and resolution.
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Support site audits/inspections/Site Compliance Visits (SCV) and ensure corrective action and follow-up for identified issues.
Supervisory Responsibilities
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Recruitment and Onboarding: Performs recruiting and hiring activities, along with onboarding new team members to ensure alignment with team objectives and culture.
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Task Assignment: Assign tasks based on individual strengths and team objectives, ensuring optimal productivity.
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Support and Resource Provision: Support team members by providing necessary resources to help them effectively perform their roles.
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Communication and Collaboration: Encourage open communication and collaboration within the team and with other functions, including acting as a point of contact for issue escalation and feedback where required.
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Performance Evaluation: Conduct regular performance evaluations and provide constructive feedback to promote continuous improvement.
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Mentoring and Development: Lead and mentor team members, fostering an environment of growth and development.
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Issue Resolution: Address any personnel issues promptly and fairly to maintain a positive work environment.
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Career Development Support: Support team members in identifying and pursuing professional development opportunities.
Qualifications
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Fluent in written and verbal English.
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Minimum 5 years of industry experience in the pharmaceutical or CRO or relevant field.
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Thorough understanding of the drug development process, including expert knowledge of international standards (ICH-GCP) and health authority requirements.
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Understanding of all aspects of monitoring and trial execution, with previous experience as a CRA preferred.
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Excellent interpersonal skills, strong organizational and effective written and verbal communication skills.
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Experience in Oncology is highly recommended.
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Proficient in Microsoft Word, Excel, PowerPoint, and Outlook.
Requirements
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Be adaptable to business trips as required per business need; require valid driver’s license in applicable countries.
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Bachelor’s degree or higher in a scientific or healthcare discipline, and advanced degrees preferred.
Benefits
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Salary Range: $105,800.00 - $140,800.00 annually.
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Participation in the annual bonus plan for Non-Commercial roles and incentive compensation plan for Commercial roles.
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Opportunity to own shares of BeOne Medicines Ltd. stock through discretionary equity awards and Employee Stock Purchase Plan.
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Comprehensive benefits package including Medical, Dental, Vision, 401(k), FSA/HSA, Life Insurance, Paid Time Off, and Wellness.
Company Description
BeOne is committed to fair and equitable compensation practices. Actual compensation packages are determined by several factors unique to each candidate, including job-related skills, depth of experience, certifications, relevant education or training, and specific work location.
We are proud to be an equal opportunity employer. BeOne does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, disability, national origin, veteran status or any other basis covered by appropriate law.
In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans’ Readjustment Assistance Act of 1974, Title I of the Americans with Disabilities Act of 1990, and any other applicable federal, state or local laws, applicants who require reasonable accommodation in the job application process may contact [email protected].