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Manage returns, cancellations, and tax invoices at Dexco, a Brazilian building materials manufacturer. Work with Salesforce, Cervello, and Sales, Logistics, and Finance teams.
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AbbVie एक वैश्विक दवा कंपनी है जो जटिल स्वास्थ्य स्थितियों के लिए औषधियों की खोज, विकास और उपलब्धता पर केंद्रित है। इसके उत्पाद पोर्टफोलियो में इम्यूनोलॉजी, ऑन्कोलॉजी, न्यूरोसाइंस और सौंदर्य चिकित्सा शामिल हैं, तथा कंपनी 175 से अधिक देशों में मरीजों की सेवा करने वाले परिचालनों के माध्यम से काम करती है। कंपनी का कार्य फार्मास्यूटिकल अनुसंधान, विनिर्माण और स्वास्थ्य सेवा विशेषज्ञता को जोड़ता है, जिसे वैज्ञानिक नवाचार तथा अनुसंधान और विकास में पर्याप्त निवेश का समर्थन प्राप्त है। AbbVie स्वास्थ्य परिणामों और समुदाय पर प्रभाव को बेहतर बनाने के अपने व्यापक दृष्टिकोण के हिस्से के रूप में विविधता, स्थिरता और मरीजों के सहयोग को भी महत्व देती है।
Remote Clinical Research Associate II, Oncology at AbbVie
Support AbbVie’s oncology clinical trials through site monitoring, investigator collaboration, and risk management. Help maintain data integrity, recruitment, compliance, and patient safety across trial activities.
विवरण
- Advance AbbVie’s clinical development pipeline through high-quality clinical research
- Act as the primary contact for investigative sites
- Provide clinical trial context and connect internal stakeholders with investigative sites
- Align, train, and motivate site staff and principal investigators on trial objectives, protocols, and patient treatment principles
- Perform site evaluation, training, routine monitoring, and closeout activities
- Maintain compliance with protocols, monitoring plans, regulations, GCPs, ICH Guidelines, SOPs, and quality standards
- Create and tailor strategies for engaging investigative sites
- Collect site insights and use CRM tools to monitor progress and assess impact
- Support trial execution by translating protocols and scientific principles into daily activities
- Assess recruitment and retention approaches in relation to the patient disease journey
- Build knowledge of therapeutic areas, assets, the clinical landscape, and patient journeys
- Mentor and train junior CRAs and contribute development feedback
- Contribute to global and local task forces and initiatives
- Perform ongoing risk assessments with the Central Monitoring team
- Address site risk signals and implement preventive and corrective action plans
- Identify and assess prospective investigators and investigative sites
- Protect data quality, timely data submission, safety-event reporting, and required follow-up
- Maintain readiness for audits and regulatory inspections
- Administer investigator payments in line with executed contract obligations, where applicable
आवश्यकताएँ
- At least one year of clinically related experience
- At least six months of clinical research monitoring experience in investigational drug or device trials
- Familiarity with risk-based monitoring, including onsite and offsite monitoring
- Knowledge of relevant therapeutic-area indications is preferred
- Advanced knowledge of local regulatory and legal requirements, ICH/GCP Guidelines, and applicable policies
- Strong ability to collaborate across functions
- Strong planning and organizational capabilities
- Ability to work effectively in a dynamic environment with competing projects and deadlines
- Ability to use technology, tools, and available resources effectively
- Strong interpersonal, written, verbal, active-listening, and presentation skills
- Ability to build site relationships and trusted partnerships
- Critical-thinking skills and sound judgment when addressing clinical site issues
- Integrity aligned with AbbVie’s code of business conduct and leadership values
- Self-motivated approach with focus on timely, high-quality outcomes
- A relevant tertiary qualification in a health-related field such as medical, scientific, or nursing is preferred
लाभ
- Paid vacation, holiday, and sick leave
- Medical, dental, and vision insurance
- 401(k) retirement plan
- Eligibility for short-term incentive programs
- Equal opportunity employer
- Reasonable accommodation is available for applicants in the United States and Puerto Rico
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