Senior Clinical Trials Manager

Job not on LinkedIn

🕒 May 8

🌵 Arizona, District of Columbia, +3 more states – Remote

🌵 Arizona – Remote 🏛️ District of Columbia – Remote 🏖️ New Jersey – Remote 🦀 Maryland – Remote 🍂 Massachusetts – Remote

💵 $127.7k - $213.5k / year

⏰ Full Time

🟠 Senior

👔 Manager

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

Apply Now

Find Similar Remote Jobs

Receive Emails For Remote 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

Agilent Technologies

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1999

🔬 Science

🧬 Biotechnology

💊 Pharmaceuticals

💰 $500M Post-IPO Debt on 2019-09

Science • Biotechnology • Pharmaceuticals

Agilent Technologies is a global leader in the field of analytical and laboratory instruments. The company offers a diverse range of products and solutions, including gas and liquid chromatography, mass spectrometry, lab supplies, and software and informatics. Agilent serves various industries, such as biopharma, food and beverage testing, clinical diagnostics, and environmental testing. Additionally, Agilent provides comprehensive services for lab management, maintenance, and instrument repair. They focus heavily on advancing science through sustainable solutions and supporting genomics, pathology, and cancer research with advanced technologies.

📋 Description

• Manage, design and implement all clinical operational aspects of IVD clinical trials from inception through close-out • Serve as main point of contact for internal and external study stakeholders; effectively communicating, collaborating, managing escalation of issues, where necessary, as well as participating and leading internal and external study meetings • Identify, evaluate, and oversee qualification and contracting for study investigators, study sites, CRO and/or vendor management for the study, where applicable • Develop or assist in the development of study-related plans and documents including protocols, informed consent forms, monitoring plans, case report forms, training plans and engagement materials • Ensure trial master file (TMF/eTMF) is established, current, and maintained per ICH E6. • Support and oversee study-related work of Clinical Research Associates (CRAs) to ensure proper site training and management • Manage study deliverables and track study metrics including identifying potential risks to study timelines and/or conduct • Review, suggest edits and approve monitoring trip reports for studies • Participate in data management activities, such as CRF development, training, and facilitating query resolution • Lead or contribute to organizational and departmental process development, improvement, and implementation • Provide guidance and mentorship to junior team members.

🎯 Requirements

• Bachelor's degree or higher, or equivalent credentials • Knowledge of GCP, ICH guidelines, and other clinical regulatory requirements • Strong interpersonal skills (verbal and written), organizational, and prioritization skills • Ability to work independently and effectively in a fast-paced environment • Strong work ethic and ability to deliver tasks on time • Proficient with office automation tools, especially Microsoft PowerPoint, Excel and Word. • For Sr CTM: 5+ years of clinical study management experience in sponsor, CRO and/or companion diagnostics, device manufacturer, IVD, or similar industry(ies) demonstrating effective and successful study management from study inception through close-out. • Experience in line management of CRAs and CTMs preferred.

🏖️ Benefits

• Bonus • Stock options • Health insurance • Paid time off • Remote work options