Clinical Research Associate I – Dermatology

🔥 4 minutes ago

🏄 California – Remote

🏄 California – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧪 Clinical Research

🚫👨‍🎓 No degree required

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

👻 Ghost score 10%

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

• Advance AbbVie's clinical research pipeline and turn science into medicine • Partner with investigators and site staff for effective clinical-trial engagements • Serve as the primary point of contact for investigative sites • Provide clinical-trial contextual 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, site training, routine monitoring, and site-closure activities under supervision • Ensure compliance with protocols, monitoring plans, regulations, GCPs, ICH Guidelines, SOPs, and quality standards • Customize site-engagement strategies for assigned studies • Gather site insights and use CRM tools to track progress and measure strategy impact • Evaluate recruitment and retention techniques based on the patient disease journey • Develop therapeutic-area, asset, clinical-landscape, and patient-journey knowledge • Conduct continuous risk assessment with the Central Monitoring team • Resolve site risk signals and implement preventative and corrective action plans • Identify, evaluate, and recommend investigators and sites under supervision • Ensure quality and timely submission of study-site data and safety-event reporting • Maintain audit and regulatory inspection readiness at assigned sites • Manage investigator payments according to executed contract obligations

🎯 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 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 work effectively in a dynamic environment with competing projects and deadlines • Ability to leverage technology, tools, and resources for customer-centric site support • Critical thinking and good judgment to address clinical site issues • Strong written, verbal, active listening, and presentation skills • Ability to establish and leverage site relationships and trusted partnerships • Integrity in accordance with AbbVie code of business conduct and leadership values • Self-motivated and focused on timely, quality outcomes • Knowledge of clinical research regulations, Good Clinical Practices (GCPs), ICH Guidelines, and AbbVie Standard Operating Procedures (SOPs)

🏖️ Benefits

• Paid time off (vacation, holidays, sick) • Medical, dental, and vision insurance • 401(k) • Eligibility to participate in short-term incentive programs • Remote work availability • Equal opportunity employment • Reasonable accommodation for US and Puerto Rico applicants