Senior Clinical Project Manager

ADP, Inc.; Baltimore (MD); Remote; USD 110,000 - 150,000; Full time

Job summary

ADP, Inc. in Baltimore, MD is seeking a Senior Clinical Research Project Manager to join our Project Management team. This role manages full-cycle clinical studies, coordinating with sponsors and internal departments, delivering timelines, budgets, and deliverables.

The position starts with an onsite training period of 1–2 weeks and transitions to fully remote work. Candidates should have 3-5+ years of clinical project management experience and PMP certification (or plan to obtain within 2

Qualifications

• Bachelor of Science in related field.
• 3-5+ years of Project Management experience in a Clinical Research environment.
• PMP Certification required or may be obtained within 2 years of hire.

Responsibilities

• Collaborates with BD team to execute site qualification and feasibility meetings.
• Work closely with department heads to evaluate costs for labor, equipment needs, and/or any other supplies needed for the protocol/synopsis.
• Collaborates with management to write, review and finalize proposal packages for sponsor submission.
• Initiates and hosts all project kick-off meetings.
• Creates integrated project timelines.
• Serves as a central point of contact with sponsors for all deliverables.
• Responsible to monitor the progress of each individual project deliverable against the project.
• Responds to sponsor post-study inquiries – collaborates with department heads.

Skills

Project management

Budget tracking

Stakeholder communication

Education

Bachelor of Science in related field

Job description

Senior Clinical Project Manager

FT-Permanent Staff Baltimore, MD USA, Baltimore, MD, US

30+ days ago Requisition ID: 1021

We are seeking a Clinical Research Project Manager to join ourBaltimore, MD Project Management team. This will be a fully remote role after an initial 1-2 week onsite training period.

As a Clinical Research Project Manager,you are responsible for full-cycle project management and act as the point person in charge of assigned studies. This role will plan, budget, monitor, and report on the project status and completion. PMs act as the bridge between sponsors, upper management, and the department heads tasked with the execution of the study.

• Collaborates with BD team to execute site qualification and feasibility meetings
• Work closely with department heads to evaluate costs for labor, equipment needs, and/or any other supplies needed for the protocol/synopsis
• Collaborates with management to write, review and finalize proposal packages for sponsor submission
• Initiates and hosts all project kick-off meetings
• Creates integrated project timelines
• Serves as a central point of contact with sponsors for all deliverables
• Responsible to monitor the progress of each individual project deliverable against the project
• Responds to sponsor post-study inquiries – collaborates with department heads

Qualifications:

• Bachelor of Science in related field
• 3-5+ years of Project Management experience in a Clinical Research environment, preferably in support of early phase and phase I studies
• Management Professional (PMP) Certification required but may be obtained within 2 years of hire or assignment