Senior Clinical Data Manager

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🏄 California, Florida, +8 more states – Remote

🏄 California – Remote 🐊 Florida – Remote 🌽 Illinois – Remote 🎰 Nevada – Remote 🗽 New York – Remote 🏈 Ohio – Remote 🦀 Maryland – Remote 🍂 Massachusetts – Remote 🤠 Texas – Remote 🍑 Georgia – Remote

💵 $86k - $1.4M / year

⏰ Full Time

🟠 Senior

🧪 Clinical Research

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Alimentiv

WebsiteLinkedInAll Job Openings

201 - 500 employees

Founded 2020

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

Alimentiv is a specialty contract research organization focused on gastrointestinal (GI) and liver diseases. With over 30 years of experience, Alimentiv offers a comprehensive range of clinical research and imaging services, including clinical trial management, site management, regulatory affairs, and precision medicine. The company is at the forefront of medical research and development, providing state-of-the-art imaging solutions and actionable biomarker insights. Alimentiv supports the development of GI compounds and is active in more than 60 countries, working with a network of medical and operational experts to accelerate clinical trials and patient recruitment.

📋 Description

• Lead, plan, and execute all data management activities for assigned projects • Ensure data integrity, validity, and reliability according to standard processes, sponsor guidelines, industry best practices, and regulatory standards • Oversee data management activities from study start-up through database lock • Create data management plans, develop CRFs and database specifications, test edit checks, and conduct data reviews • Coordinate database builds and testing with programmers • Define and validate edit checks, perform query management, and process/reconcile electronic data from CIMS, Safety database, labs, and IRT • Coordinate and supervise 1-7 Data Management staff members • Provide training, mentorship, and performance reviews while managing project resources within budget and timelines • Participate in and lead internal and sponsor meetings • Collaborate with project managers and teams, track study progress, issue status reports, and escalate data-related issues • Develop and deliver training for investigators, clinical sites, project teams, and sponsors • Maintain and properly store study documentation in trial master files • Contribute to continuous improvement, SOPs, policies, and cross-functional working groups • Act as a Subject Matter Expert and support process improvements, issue escalation, and data management excellence • Ensure compliance with standard processes, sponsor guidelines, industry best practices, and regulatory standards

🎯 Requirements

• A minimum of a one-to-two-year post-secondary certification in a relevant field of study • 4-6 years of related work experience in Clinical Data Management with ongoing training • Life Sciences or Clinical Research specialty preferred • CCDM (Certified Clinical Data Manager) certification preferred • Ability to set personal pace and prioritize tasks with significant autonomy • Strong interpersonal skills with patience and tact for managing regular contacts with team members, vendors, and clients • Resumes must be submitted in English

🏖️ Benefits

• Education Reimbursement program for full-time employees • Monthly Cell Phone and Remote Work Allowance (dependent on role eligibility) • One time office setup allowance • Working while visiting program – up to 4 weeks per year • Flexible Summer Hours Program from May – September • Employee referral incentive • Alimentiv Trust beneficiary after one year of employment and permanent membership after 5 years of employment for full-time employees • Optional formal mentorship program (Alimentorship) • Country/region annual social events in person • Leadership development programs for people leaders according to seniority • Social committee and other optional initiatives • Additional benefits may be available depending on country of employment and local policies and eligibility

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