Job Description:
- Advance AbbVie's pipeline by striving for excellence in clinical research, turning science into medicine for our patients
- Partners with the investigator and site staff for meaningful and effective engagements positioning AbbVie as the choice in clinical trials
- Focus on site clinical research that ensures appropriate conduct of the trial while driving improvement in data integrity, compliance, overall study performance and customer experience
- Considered as the primary point of contact for the investigative site, provides contextual information on the clinical trials, connects stakeholder to the investigative sites and strengthens AbbVie’s positioning
- Aligns, trains and motivates the site staff and principal investigator under supervision on the goals of the clinical trial program, protocol, and patient treatment principles for the trial ensuring a trusted partnership
- Conducts site evaluation, site training, routine, and site closure monitoring activities under supervision, in compliance to the protocol and monitoring plans and accordance with applicable regulations, Good Clinical Practices (GCPs), ICH Guidelines, AbbVie Standard Operating Procedures (SOPs), and to quality standards in conducting clinical research, ensuring safety and protection of study subjects
- Customize site engagement strategy for assigned study (ies) under supervision
- Gather local/site insights and utilize site engagement tools such as the Customer Relationship Management (CRM) tool, to report/track progress and measure impact of that strategy
- Evaluate and ensure effective recruitment and retention techniques/plans based on the patient disease journey
- Responsible for continuous risk-assessment proactively, and in collaboration with Central Monitoring team, monitor activities conducted by clinical sites to detect early overall study performance or patient safety issues
- Ensures preventative and corrective action plans are put into place, as needed, to mitigate risk and promote compliance
Requirements:
- Appropriate tertiary qualification in health related disciplines (Medical, Scientific, Nursing) preferred or experience or equivalent work experience
- Clinically related experience, preferably in clinical research coordinating or data management
- Knowledge of appropriate therapeutic area indications is preferred with the ability to understand and apply scientific concepts as they relate to the conduct of clinical trials
- Knowledge on existing and emerging local regulatory and legal requirements, ICH/GCP Guidelines and applicable policies
- Able to work collaboratively and cross functionally to develop and sustain working relationships
- Demonstrate planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines
- Ability to leverage technology, tools and resources to provide customer centric support based on the health of the site
- Ability to use functional expertise with appropriate guidance, leverage critical thinking skills and apply good judgement to address clinical site issues
- Interpersonal skills with strong written, verbal, active listening and presentation skills, with ability to establish and leverage site relationships and trusted partnerships through engagement, motivation, and training
- Acts with integrity in accordance with AbbVie code of business conduct and leadership values
- Self-motivated individual focused on delivering timely and quality outcomes in a fast-paced environment.
Benefits:
- paid time off (vacation, holidays, sick)
- medical/dental/vision insurance
- 401(k) to eligible employees
- short-term incentive programs
About the Clinical Research Associate I – Oncology Opportunity
AbbVie is currently hiring for a Clinical Research Associate I – Oncology position based in Remote. This is a full time opportunity suited to candidates who are ready to contribute their skills and grow within a dynamic team environment. Whether you're an experienced professional or looking to take the next step in your career, this role offers a chance to work on meaningful projects while developing new capabilities.
What the Role Involves
As a Clinical Research Associate I – Oncology, you will be expected to collaborate closely with cross-functional teams, take ownership of key deliverables, and contribute ideas that help AbbVie achieve its goals. Day-to-day responsibilities typically include planning and prioritizing tasks, communicating progress with stakeholders, maintaining high standards of quality, and adapting to evolving business needs. The exact scope of duties may vary depending on team structure and current priorities, so candidates should be comfortable with a role that can evolve over time.
Who AbbVie is Looking For
Successful candidates generally bring a combination of relevant experience, strong communication skills, and a proactive attitude toward problem-solving. AbbVie values individuals who can work independently as well as part of a team, who are detail-oriented, and who bring a positive, adaptable mindset to their work. Prior experience in a similar Clinical Research Associate I – Oncology capacity is beneficial, though a strong willingness to learn and grow is equally important.
Compensation and Benefits
This role offers a compensation package of approximately USD 75000 - 142500 per year, commensurate with experience. In addition to base pay, many roles at AbbVie may include benefits such as health coverage, paid time off, opportunities for professional development, and a supportive work culture designed to help employees thrive both personally and professionally.
Why Join AbbVie?
Joining AbbVie as a Clinical Research Associate I – Oncology means becoming part of a team that values collaboration, innovation, and continuous improvement. Employees are encouraged to bring their own perspective to the table, and the organization aims to foster an environment where people feel supported in doing their best work. This is a great opportunity for candidates who want their contributions to have a real, visible impact.
How to Apply
If you believe you're a strong fit for the Clinical Research Associate I – Oncology role at AbbVie in Remote, we encourage you to review the full job details above and submit your application through the listed channel. This position was posted on 2026-07-01 and applications are being accepted through 2026-09-29. Early applications are generally encouraged, as competitive roles like this one can attract a high volume of interest.
