
10,000+ employees
Founded 2013
🏥 Healthcare
💼 Consulting
🏭 Manufacturing
Healthcare • Consulting • Manufacturing
AbbVie is a global pharmaceutical company that discovers and delivers innovative medicines and solutions to enhance lives. With a focus on addressing the world's toughest health challenges, AbbVie operates in over 175 countries, providing a wide range of products across areas like immunology, oncology, neuroscience, and aesthetics. Committed to scientific innovation, AbbVie invests heavily in research and development, aiming to produce first-in-class medicines. The company also emphasizes workplace diversity, sustainability, and patient support initiatives, ensuring positive impact for both its patients and the broader community.
🔥 0 minutes ago
🤠 Texas – Remote
💵 $75k - $142.5k / year
⏰ Full Time
🟢 Junior
🟡 Mid-level
🧪 Clinical Research
🚫👨🎓 No degree required
🦅 H1B Visa Sponsor
Improve your chances of getting an interview by checking your resume score before you apply.

10,000+ employees
Founded 2013
🏥 Healthcare
💼 Consulting
🏭 Manufacturing
Healthcare • Consulting • Manufacturing
AbbVie is a global pharmaceutical company that discovers and delivers innovative medicines and solutions to enhance lives. With a focus on addressing the world's toughest health challenges, AbbVie operates in over 175 countries, providing a wide range of products across areas like immunology, oncology, neuroscience, and aesthetics. Committed to scientific innovation, AbbVie invests heavily in research and development, aiming to produce first-in-class medicines. The company also emphasizes workplace diversity, sustainability, and patient support initiatives, ensuring positive impact for both its patients and the broader community.
• Serve as the primary point of contact for investigative sites and provide clinical trial information. • Connect stakeholders with investigative sites and strengthen AbbVie’s positioning in clinical trials. • Align, train, and motivate site staff and principal investigators on trial goals, protocols, and patient treatment principles. • Conduct site evaluation, training, routine monitoring, and site closure activities under supervision. • Customize site engagement strategies and track progress using CRM tools. • Apply protocol, scientific, and clinical trial knowledge to day-to-day trial execution. • Evaluate and support patient recruitment and retention plans. • Monitor site activities and assess risks to study performance and patient safety. • Resolve site risk signals and implement preventative and corrective action plans. • Identify and recommend potential investigators and sites. • Ensure data quality, timely data submission, safety-event reporting, and follow-up. • Maintain audit and regulatory inspection readiness. • Manage investigator payments according to executed contracts, as applicable.
• Appropriate tertiary qualification in a health-related discipline (Medical, Scientific, Nursing) preferred, or equivalent work experience. • Clinically related experience, preferably in clinical research coordinating or data management. • Knowledge of therapeutic-area indications preferred. • Ability to understand and apply scientific concepts to clinical trial conduct. • Knowledge of local regulatory and legal requirements, ICH/GCP Guidelines, and applicable policies. • Ability to work collaboratively and cross-functionally. • Planning and organizational skills; ability to manage competing projects and deadlines. • Ability to leverage technology, tools, resources, and CRM systems. • Critical-thinking and judgment skills for addressing clinical-site issues. • Strong written, verbal, active-listening, and presentation skills. • Ability to establish site relationships through engagement, motivation, and training. • Integrity in accordance with AbbVie’s code of business conduct and leadership values. • Self-motivated approach focused on timely, quality outcomes. • Willingness to travel 75% of the time.
• Paid time off (vacation, holidays, sick) • Medical, dental, and vision insurance • 401(k) • Eligibility to participate in short-term incentive programs • Remote work arrangement
Apply Now🕒 Yesterday
Biostatistician analyzing complex longitudinal registry data for Thermo Fisher’s real-world evidence and drug-safety research. Developing statistical analyses, reports, and publications for clinical and regulatory programs.
🕒 2 days ago
Clinical Research Associate monitoring clinical trials for ICON, a global healthcare intelligence and clinical research organization. Ensuring protocol compliance, data integrity, patient safety, and quality study documentation.
🕒 2 days ago
Associate Clinical Trial Manager supporting Phase 1–3 clinical trials at 4DMT, a biotechnology company developing disease-targeted therapeutics. Coordinating trial operations, vendors, regulatory documents, data, and close-out activities.
🇺🇸 United States – Remote
💵 $117k - $132k / year
⏰ Full Time
🟢 Junior
🟡 Mid-level
🧪 Clinical Research
🦅 H1B Visa Sponsor
🕒 2 days ago
Clinical Research Associate II monitoring NMDP-sponsored multi-center clinical trials. Supporting site management, compliance, training, and cellular therapy research advancing patient outcomes.
🕒 2 days ago
Clinical research and financial analyst supporting Tenet Health clinical trials, budgets, billing, data analysis, and regulatory compliance. Preparing study reports and maintaining accurate research records.
🇺🇸 United States – Remote
💰 $2G Post IPO debt on 2022-07
⏰ Full Time
🟢 Junior
🟡 Mid-level
🧪 Clinical Research