Clinical Research Associate

🔥 0 minutes ago

Apply Now
Find Similar Remote Jobs

📊 Check your resume score for this job

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

Logo of ICON plc

ICON plc

10,000+ employees

Founded 1990

💊 Pharmaceuticals

🧬 Biotechnology

⚕️ Healthcare Insurance

Pharmaceuticals • Biotechnology • Healthcare Insurance

ICON plc is a global provider of clinical, consulting, and commercial services across various sectors in the healthcare and pharmaceutical industries. They offer a wide range of clinical solutions, including decentralised clinical trials, cardiac safety solutions, early clinical laboratories, and medical imaging. ICON also provides technology solutions that support drug development from early phases to post-marketing. Their therapeutic expertise spans cardiovascular, oncology, internal medicine, and more, with a strong focus on transformative therapies like cell and gene therapies and biosimilars. ICON is recognized as a leading Contract Research Organisation (CRO), regularly providing thought leadership and contributing to industry publications and events. Their services are tailored to optimize clinical trials, offer regulatory intelligence, and deliver real-world evidence through robust data analysis and patient-centric solutions.

📋 Description

• Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials • Ensuring protocol compliance, data integrity, and patient safety throughout the trial process • Collaborating with investigators and site staff to facilitate smooth study conduct • Performing data review and resolution of queries to maintain high-quality clinical data • Contributing to the preparation and review of study documentation, including protocols and clinical study reports

🎯 Requirements

• Bachelor's degree in a scientific or healthcare-related field highly preferred • Minimum of 2 years of experience as a Clinical Research Associate • In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines • Strong organizational and communication skills, with attention to detail • Ability to work independently and collaboratively in a fast-paced environment • Ability to travel at least 60% of the time (international and domestic - fly and drive) • Must possess a valid driver’s license

🏖️ Benefits

• Competitive base salary and performance related incentives • Health and wellbeing programmes including medical, dental, and vision coverage where applicable • Retirement and pension plans • Life assurance and disability coverage • Employee assistance programmes and wellbeing resources • Learning and development opportunities through structured training and career pathways

Apply Now

Similar Jobs

🔥 1 hour ago

AbbVie

10,000+ employees

💊 Pharmaceuticals

🧬 Biotechnology

⚕️ Healthcare Insurance

Clinical Research Associate II at AbbVie engaging investigative sites in oncology trials. Driving clinical research excellence while ensuring safety and data integrity for clinical studies.

🔥 11 hours ago

Providence

10,000+ employees

⚕️ Healthcare Insurance

Research Analyst focusing on claims payment accuracy and integrity within Providence Health Plan. Collaborating with stakeholders to implement improvements and prevent unnecessary spending.

🔥 23 hours ago

AbbVie

10,000+ employees

💊 Pharmaceuticals

🧬 Biotechnology

⚕️ Healthcare Insurance

Clinical Research Associate II focusing on Neuro & Immunology at AbbVie in Chicago, with responsibilities in trial execution and site engagement.

🔥 23 hours ago

AbbVie

10,000+ employees

💊 Pharmaceuticals

🧬 Biotechnology

⚕️ Healthcare Insurance

Clinical Research Associate II managing clinical trials for AbbVie focusing on oncology. Ensuring compliance, mentoring junior staff, and collaborating with various stakeholders.

🔥 23 hours ago

Perspective Therapeutics

51 - 200

🧬 Biotechnology

⚕️ Healthcare Insurance

💊 Pharmaceuticals

Clinical Research Associate II at Perspective Therapeutics specializing in oncology trials. Collaborate with cross-functional teams to ensure compliance with clinical trial protocols and standards.