Clinical Trial Coordinator

Job not on LinkedIn

🔥 1 minute ago

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

Thermo Fisher Scientific

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1956

🧬 Biotechnology

💊 Pharmaceuticals

🔬 Science

Biotechnology • Pharmaceuticals • Science

Thermo Fisher Scientific is the world leader in serving science, with annual revenue of more than $40 billion. Their mission is to enable customers to make the world healthier, cleaner, and safer by supporting life sciences research, solving complex analytical challenges, increasing laboratory productivity, and improving patient health through diagnostics and the development of life-changing therapies. With a global team, they offer innovative technologies and pharmaceutical services through brands such as Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD.

📋 Description

• Join as a Clinical Trial Coordinator and provide administrative and technical support to the Project Team. • Support audit readiness by ensuring files are reviewed according to the schedule. • Provide administrative support for site activation activities. • Develop collaborative relationships with investigators and site personnel. • Analyze and reconcile study metrics and findings reports. • Maintain vendor trackers and assist with study-specific materials.

🎯 Requirements

• High / Secondary school diploma or equivalent and relevant formal academic / vocational qualification. • Bachelor's degree preferred. • Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to at least 2 years). • Ability to work in a team or independently, as required. • Strong organizational skills and attention to detail, with proven ability to handle multiple tasks efficiently and effectively. • Proven ability to effectively analyze project-specific data/systems to ensure accuracy and efficiency. • Strong customer focus. • Demonstrated flexibility and adaptability to reprioritize workload and provide efficient support to meet changing project timelines. • Excellent English language and grammar skills and proficient local language skills as needed. • Good presentation skills. • Excellent computer skills, proficient in MS Office (Word, Excel, and PowerPoint) and ability to obtain knowledge and master all clinical trial database systems. • Self-motivated, positive attitude with effective strong interpersonal skills. • Effective oral and written communication skills, with the ability to communicate effectively with medical personnel. • Basic medical/therapeutic area and medical terminology knowledge. • Ability to attain and maintain a working knowledge of GCP and applicable SOPs. • Excellent customer focus. • Proven flexibility and adaptability.

🏖️ Benefits

• Flexible work arrangements