Associate​/Clinical Project Manager; Client Dedicated

NaSPA, Inc.

Lewisville, TXFull-timePosted Apr 5, 2026

60K–80K a year

Behavioral Health Market Context

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Job Description

 contractual requirements in accordance with SOPs, policies and Company practices. Clinical Project Management is focused on project delivery, productivity and quality resulting in strong financial performance and customer satisfaction.

The Associate Clinical Project Manager has distinct responsibilities supporting the efforts of the Clinical Project Manager to drive operational excellence and strategic leadership with our customers. Associate Clinical Project Managers may run their own studies as part of their development and/or manage the Project's Third-Party Vendors.
Essential Functions
• Provide input in to the development of integrated study management plans with the core project team and/or sub-team, within a client-dedicated team.
• Accountable for assigned portion of clinical studies as per the contract while optimizing speed, quality and cost of delivery and ensuring consistent use of study tools and training materials and compliance with standard processes, policies and procedures.
• Set objectives of project sub-team(s), according to agreed upon contract, strategy and approach, effectively communicate and assess performance.
• Collaborate with other functional groups within the company where necessary to support milestone achievement and to manage study issues and obstacles.
• Monitor progress against contract and prepare/present project and/or sub-team information proactively to internal stakeholders. Support the project leader to prepare/present project and/or sub-team information proactively to external stakeholders.
• Identify risk (positive and negative) and contingencies and partner with project leader in problem solving and resolution efforts.
• Achieve project quality by identifying quality risks and issues, responding to issues raised by project sub-team members and partner with project leader planning/implementing appropriate corrective and preventative action plans.
• May serve as primary (for small projects) or back-up project contact with customer.
• Lead the efforts of a project sub-team, responsible for managing cross-collaboration of the sub-team to support milestone achievement and to manage issues and obstacles.
• Support the project leader in ensuring the financial success of the project.
• Forecast and identify opportunities to accelerate activities to bring revenue forward in partnership with the senior project leader.
• Identify changes in scope and partner with project leader to manage change control process as necessary.
• Identify lessons learned and implement best practices.
• May be assigned as the primary contact for vendors leading project vendor management and vendor management related activities as per project requirements
Qualifications
• Bachelor's Degree In life sciences or related field required
• More than 1 year of Clinical lead, Clinical Trials Manager, Project Management experience preferred.
• Knowledge of clinical trials - Knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements i.e. ICH GCP and relevant local laws, regulations and guidelines, towards clinical trial conduct. Broad protocol knowledge, therapeutic knowledge desired.
• Communication - Strong written and verbal communication skills including good command of English language. Strong presentation skills.
• Problem solving - Strong problem solving skills.
• Organisation - Planning, time management and prioritization skills. Ability to organize resources needed to accomplish tasks, set objectives and provide clear direction to others, experience planning activities in advance and taking account of possible changing circumstances.
• Prioritisation - Ability to handle conflicting priorities.
• Quality - Attention to detail and accuracy in work. Results-oriented approach to work towards delivery and output.
• IT Skills - Good software and computer skills, including MS…

Qualifications

  • Bachelor's Degree In life sciences or related field required
  • Knowledge of clinical trials - Knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements i.e
  • ICH GCP and relevant local laws, regulations and guidelines, towards clinical trial conduct
  • Strong presentation skills
  • Problem solving - Strong problem solving skills
  • Organisation - Planning, time management and prioritization skills
  • Ability to organize resources needed to accomplish tasks, set objectives and provide clear direction to others, experience planning activities in advance and taking account of possible changing circumstances
  • Prioritisation - Ability to handle conflicting priorities
  • Quality - Attention to detail and accuracy in work
  • Results-oriented approach to work towards delivery and output
  • IT Skills - Good software and computer skills, including MS…

Benefits

    Responsibilities

    • Associate Clinical Project Managers are an integral part of clinical trial delivery, liaising with clinical teams to improve patients' lives by bringing new drugs to the market faster
    • The Associate Clinical Project Manager is a member of the core project team responsible for project delivery of clinical studies to meet contractual requirements in accordance with SOPs, policies and Company practices
    • Clinical Project Management is focused on project delivery, productivity and quality resulting in strong financial performance and customer satisfaction
    • The Associate Clinical Project Manager has distinct responsibilities supporting the efforts of the Clinical Project Manager to drive operational excellence and strategic leadership with our customers
    • Associate Clinical Project Managers may run their own studies as part of their development and/or manage the Project's Third-Party Vendors
    • Provide input in to the development of integrated study management plans with the core project team and/or sub-team, within a client-dedicated team
    • Accountable for assigned portion of clinical studies as per the contract while optimizing speed, quality and cost of delivery and ensuring consistent use of study tools and training materials and compliance with standard processes, policies and procedures
    • Set objectives of project sub-team(s), according to agreed upon contract, strategy and approach, effectively communicate and assess performance
    • Collaborate with other functional groups within the company where necessary to support milestone achievement and to manage study issues and obstacles
    • Monitor progress against contract and prepare/present project and/or sub-team information proactively to internal stakeholders
    • Support the project leader to prepare/present project and/or sub-team information proactively to external stakeholders
    • Identify risk (positive and negative) and contingencies and partner with project leader in problem solving and resolution efforts
    • Achieve project quality by identifying quality risks and issues, responding to issues raised by project sub-team members and partner with project leader planning/implementing appropriate corrective and preventative action plans
    • May serve as primary (for small projects) or back-up project contact with customer
    • Lead the efforts of a project sub-team, responsible for managing cross-collaboration of the sub-team to support milestone achievement and to manage issues and obstacles
    • Support the project leader in ensuring the financial success of the project
    • Forecast and identify opportunities to accelerate activities to bring revenue forward in partnership with the senior project leader
    • Identify changes in scope and partner with project leader to manage change control process as necessary
    • Identify lessons learned and implement best practices
    • May be assigned as the primary contact for vendors leading project vendor management and vendor management related activities as per project requirements


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