Associate Project Manager

OverviewLabConnect improves lives by partnering with pharmaceutical and biotech companies, and clinical research organizations (CROs) to accelerate the development of new medicines around the world.We are an independent, global, one-stop-shop focused on delivering Central Laboratory Services that are tailor-made, timely and flexible to meet the evolving study demands of traditional to increasingly complex trials. Additionally, we provide Functional Service Provider (FSP) Solutions, supporting our clients with scientific and technical expertise, acting as an extension of their team, coordinating all laboratory related needs, advising on strategies for lab data collection and providing end-to-end analytical and logistical solutions. SummaryThe Associate Project Manager, Project Management, will assist the Project Managers with daily tasks in managing projects to client specifications, ensuring quality deliverables are on time and within budget.This position is remote and is based in the US.ResponsibilitiesWorks closely with project managers to assist in study oversight processes, and for training and development towards becoming a project manager. Will work as project assigned co-PM supporting lead PM or Sr. PM.  After 6 months, a PM may be assigned to independently lead low complexity, single region projects. Independently led projects are not to exceed 50% of a PM capacity, with > 50% of assigned project support to be co-PM for at least first 18 months in this role.     Provides backup to the PM for ongoing oversight for clinical trial projects assigned.Assists with review of IT database validations and assures they are completed prior to specimen receipt and reporting for specific project. Assists in maintaining study status in SharePoint.Perform Quality Control (QC) checks on the kit builds. Liaise with Project Coordinators to ensure study-related tasks required have are performed.Maintenance of project Dashboard including risk register (portions may be delegated) Schedule meetings for the hand-off of projects from Project Set-Up to the PM and assists with project-specific training of internal staff, as well as handover.Secondary project contact with Sponsors and Contract Research Organizations to ensure appropriate communication channels are maintained and reporting schedules adhered to.Review of reports and documents, including enrollment logs, pending test reports, global lab reporting, issue logs, and shipping manifests, as part of study oversight.As needed, interfaces with laboratory(ies), BD, Operations, and Data Management to communicate study needs or for problem solving.Liaise with the assigned data manager to ensure data is delivered on time per the SOW.Assist with collection of quality and performance related metrics to assess the success of study oversight activities.Assist the PM with requests for shipment of stored samples as directed in the SOW, and coordinate with Biorepository staff to ensure samples are shipped on time.Assists PM in ensuring that all laboratory requirements outlined in the protocol are managed per expectations and in compliance with laboratory practices.Creates training materials for investigator meetings as applicable.Works with Quality and Regulatory Services in archiving study documents after study close.Performs other related duties and tasks as necessary or as assigned.Education and QualificationsBachelor's degree (B.A./B.S.) from four-year college or university; and one to two years central laboratory project support experience.Associates degree (A.A/A.S) will be considered if combined with 3+ years of central laboratory project support experience.  Must be experienced in customer service.Possess excellent organization and adaptability.Must have interpersonal skills and excellent communication skills.Preferred clinical trial support experience.Must be adept at stress management.Must be proactive and productive.Language AbilityAbility to read, analyze, and interpret general business periodicals, professional journals, or technical procedures.  Ability to write business correspondence and procedure manuals.  Ability to effectively present information and respond to questions from managers and clients.Math Ability Ability to perform calculations and manage budgets.  Ability to apply mathematical concepts to budget management for clinical trials and metrics analysis. Reasoning AbilityAbility to solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists. Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form.Computer SkillsTo perform this job successfully, the individual must be proficient in Microsoft Office applications including Outlook, Word processing, Excel, and PowerPoint. SharePoint, Salesforce, and Microsoft Visio experience a plus.Certificates and LicensesCertification as an ASCP Medical Technologist and/or Registered Nurse is beneficial but not required. Supervisory Responsibilities  This position has no supervisory responsibilities.  Work Environment  The noise level in the work environment is usually moderate.  Physical Demands  While performing the duties of this job, the employee is frequently required to sit, talk and hear.  The employee is occasionally required to stand; walk and reach with hands and arms.  The employee must occasionally lift and/or move up to 30 pounds.  Specific vision abilities required by this job include close vision and ability to adjust focus. Join our team and discover how your work can impact patients' lives around the world Some of the Perks our LabConnectors Love: We truly live our values: People First, Quality Focused, Customer Centered, Technology Driven and Accountability Always The opportunity to make a meaningful impact on a passionate and growing team Strong communication and collaboration within a smaller sized team Access to tools and resources that empower you to excel in your role In addition to great perks and challenging work assignments, we invest in our people with enriching career growth opportunities, globally. We believe in a friendly and collaborative environment with open lines of communication. We are proud to be an Equal Opportunity Employer and value the diversity of our workforce. We do not discriminate on the basis of race, gender, age, disability, religion, sexual orientation, or any other protected characteristic.  LabConnect also prioritizes the privacy and security of your personal data. All candidate information is handled in accordance with the General Data Protection Regulation (GDPR). For this job posting, all hiring decisions are made with meaningful human involvement and consideration. In this context, no applicant is subject to a decision based solely on automated processing within the meaning of Article 22 of the GDPR.   To learn more, please review our Privacy Notice on our website, by navigating to  If you need assistance to complete your job application, search for a job opening, or submit an online application at LabConnect - please email or call