Clinical Research Associate II

🕒 August 13

⚔️ Virginia – Remote

⚔️ Virginia – Remote

💵 $78.5k - $141k / year

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧪 Clinical Research

🚫👨‍🎓 No degree required

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

👻 Ghost score 0%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

Apply Now

Find Similar Remote Jobs

Set Up Email Alert For New Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume

AbbVie

WebsiteLinkedInAll Job Openings

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.

📋 Description

• Serve as the primary point of contact for investigative sites • Provide clinical trial information and connect stakeholders with investigative sites • 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 • Ensure compliance with protocols, monitoring plans, regulations, GCPs, ICH Guidelines, SOPs, and quality standards • Develop and customize site engagement strategies and track progress using CRM tools • Evaluate recruitment and retention techniques based on the patient disease journey • Mentor and train less experienced CRAs • Participate in global or local task forces and initiatives • Conduct continuous risk assessment in collaboration with the Central Monitoring team • Resolve site risk signals and implement preventative and corrective action plans • Identify and evaluate potential investigators and clinical trial sites • Ensure data quality, timely data submission, and appropriate safety-event reporting • Maintain audit and regulatory inspection readiness • Manage investigator payments according to contract obligations

🎯 Requirements

• Appropriate tertiary qualification in health-related disciplines (Medical, Scientific, Nursing) preferred • Minimum of 1 year of clinically related experience • At least 6 months of clinical research monitoring experience with investigational drug or device trials • Familiarity with risk-based monitoring, including onsite and offsite monitoring • Knowledge of applicable therapeutic area indications preferred • Ability to understand and apply scientific concepts to clinical trial conduct • Advanced knowledge of local regulatory and legal requirements, ICH/GCP Guidelines, and applicable policies • Strong cross-functional collaboration skills • Strong planning and organizational skills • Ability to work effectively in a dynamic environment with competing projects and deadlines • Advanced ability to leverage technology, tools, and resources • Strong interpersonal, written, verbal, active listening, and presentation skills • Ability to establish and leverage site relationships through engagement, motivation, and training • Critical thinking and sound judgment to address clinical site issues • Integrity consistent with AbbVie’s code of business conduct and leadership values • Self-motivated with focus on timely, quality outcomes in a fast-paced environment

🏖️ Benefits

• Paid time off (vacation, holidays, sick) • Medical, dental, and vision insurance • 401(k) • Short-term incentive programs • Equal opportunity employer • Reasonable accommodation for applicants with disabilities