Clinical Trials Project Manager

🕒 September 24

🗽 New York – Remote

🗽 New York – Remote

💵 $80k - $100k / year

⏰ Full Time

🟢 Junior

👷‍♀️ Project Manager

🚫👨‍🎓 No degree required

👻 Ghost score 10%

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ACM Global Laboratories

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

ACM Global Laboratories is a leading provider of clinical trial testing services, supporting clinical trials globally in over 65 countries. The company offers a range of bioanalytical services, including small and large molecule analysis, biomarker analysis, and various laboratory testing solutions such as routine safety testing, flow cytometry, and advanced sample tracking. ACM Global Laboratories is recognized for its expertise in bioanalysis and toxicology services, ensuring high sensitivity and accuracy in drug and metabolite measurements across diverse biological samples. The company is dedicated to delivering actionable clinical insights and reliable toxicology services to healthcare providers, partnering with clinical trials to optimize development projects through state-of-the-art laboratory services, specimen management, and global logistics.

📋 Description

• Liaise with ACM Global Central Laboratory clients as the laboratory representative for clinical trials • Serve as the client’s primary point of contact and maintain customer service and satisfaction • Liaise internally to ensure trials follow the Global Laboratory Specification Document • Manage assigned clinical trials from setup through maintenance and study closeout • Review clinical protocols and assist with protocol setup • Develop the Global Laboratory Specification Document, Investigator Manual, and protocol-specific Global Work Practice Instructions • Participate in and document clinical trial quality audits and inspections • Evaluate and communicate monthly project metrics • Analyze trial activity, including monthly budget review • Conduct investigator training sessions by telephone or at investigator meetings • Attend client events and international ACM locations as needed • Ensure client goals and timelines are met; troubleshoot and solve problems • Perform assigned on-call coverage duties • Manage regulatory-required study documentation, including collection, maintenance, and archiving • Develop protocol-specific procedures as needed • Follow company policies, procedures, and applicable clinical research regulations

🎯 Requirements

• 1+ years project management experience • Bachelor’s Degree is preferred • Experience working in a clinical trial, laboratory or healthcare setting is preferred • Excellent problem solving and communication skills • General working knowledge of FDA, NYSDOH, GCP, ICH and other pertinent regulations as they pertain to central laboratory functions • Ability to travel overnight, frequently on weekend days • Ability to travel to client events and ACM international locations • Passport qualifications • Ability to take assigned on-call coverage duties • Ability to maintain patient and client confidentiality • Ability to manage 10 to 25 protocols after training, depending on scope and complexity • Ability to manage more than $3,000,000 in contract value and maintain more than 120 PM billable hours per month • Sedentary work capacity, including prolonged sitting and minimal lifting under 10 lbs • Clear visual and auditory ability and fine motor skills for computer work, writing, and telephone use

🏖️ Benefits

• Overnight travel for investigator training sessions, client events, and ACM international locations • Potential additional pay components • Consideration for flexible hours and accommodations where applicable