ZipRecruiter

Log In

1

Associate Clinical Project Manager Jobs in Arizona

Acadia Healthcare

Associate Clinical Director

Tucson, AZ

$68K - $93K/yr

Sierra Tucson is seeking an experienced Associate Clinical Director to join our team! Since 1984 ... Develop plans for improvement as needed. · Provide staff management to including hiring ...

Sierra Tucson

Associate Clinical Director

Tucson, AZ

$68K - $93K/yr

Overview Sierra Tucson is seeking an experienced Associate Clinical Director to join our team ... Provide staff management to including hiring, development, training, performance management and ...

Acadia Healthcare

Associate Clinical Director

Tucson, AZ · On-site

$68K - $93K/yr

Overview Sierra Tucson is seeking an experienced Associate Clinical Director to join our team ... Develop plans for improvement as needed. • Provide staff management to including hiring ...

Sierra Tucson

Associate Clinical Director

Tucson, AZ · On-site

Overview Sierra Tucson is seeking an experienced Associate Clinical Director to join our team ... Provide staff management to including hiring, development, training, performance management and ...

AHEAD

Associate Project Manager

Phoenix, AZ · On-site

$80K - $88K/yr

Associate Project Manager The Associate Project Manager concentrates on learning the basics of Project Management and developing the skills necessary to begin a career in Project Management. The APM ...

PHI Health

Clinical Training Manager

Tempe, AZ · On-site

$62K - $85K/yr

By integrating education, systems oversight, compliance, and project management, this position fosters professional development, drives innovation in training, and ensures alignment of clinical ...

PHI Health

Clinical Training Manager

Tempe, AZ

$62K - $85K/yr

By integrating education, systems oversight, compliance, and project management, this position fosters professional development, drives innovation in training, and ensures alignment of clinical ...

BioLab Holdings, Inc.

Project Manager

Mesa, AZ · On-site

... deliver clinical performance and real-world impact. Position Summary We are seeking a detail ... The Project Manager will collaborate cross-functionally with teams in Research & Development ...

InterSources Inc

Project Manager

Mesa, AZ · On-site

They are seeking a Project Manager with a strong healthcare background to assist with a ... Required : • Strong healthcare background especially on the clinical side to help with the ...

Inizio Evoke

Project Manager

Tempe, AZ · On-site +1

You will report to the Associate Director, Project Management. This is a remote role. As a Project Manager, you: * Play an integral role in all decisions regarding process, project resources, budgets ...

Allied Universal

Project Manager

Phoenix, AZ · On-site

Associates Degree preferred * At least six years of project management experience, electronic security industry experience is preferred * A proven track record and verified references relating to the ...

next page

Showing results 1-20

All JobsAssociate Clinical Project JobsAssociate Clinical Project Manager JobsAssociate Clinical Project Manager Jobs in Arizona

Associate Clinical Project Manager information

See Arizona salary details

$15

$36

$55

How much do associate clinical project manager jobs pay per hour?

As of Jun 10, 2026, the average hourly pay for associate clinical project manager in Arizona is $36.11, according to ZipRecruiter salary data. Most workers in this role earn between $27.79 and $41.88 per hour, depending on experience, location, and employer.

What is an Associate Clinical Project Manager?

An Associate Clinical Project Manager (ACPM) is an entry- to mid-level professional who assists in planning, coordinating, and overseeing clinical trials and research projects within pharmaceutical, biotech, or clinical research organizations. They work closely with project managers and cross-functional teams to ensure studies are conducted according to protocol, regulatory requirements, and timelines. ACPMs may handle tasks such as tracking project progress, supporting site management, preparing documentation, and communicating with stakeholders. Their role helps ensure the smooth execution and delivery of clinical research projects.

What are the common challenges faced by an Associate Clinical Project Manager and how can they be addressed?

Associate Clinical Project Managers often encounter challenges such as balancing multiple study timelines, coordinating cross-functional teams, and ensuring regulatory compliance. Managing communication between sponsors, vendors, and internal teams can also be complex. To address these challenges, it's important to prioritize tasks, maintain clear documentation, and foster strong relationships with stakeholders. Leveraging project management tools and regularly reviewing project milestones can help ensure studies stay on track and issues are promptly resolved.

What are the key skills and qualifications needed to thrive as an Associate Clinical Project Manager, and why are they important?

To thrive as an Associate Clinical Project Manager, you need a solid understanding of clinical research processes, project management principles, and typically a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and Good Clinical Practice (GCP) certification is often required. Exceptional organizational skills, attention to detail, and strong communication abilities help you coordinate teams and timelines effectively. These competencies are crucial for ensuring clinical trials run smoothly, meet regulatory standards, and deliver reliable results on schedule.

What is the difference between Associate Clinical Project Manager vs Clinical Project Coordinator?

AspectAssociate Clinical Project ManagerClinical Project Coordinator
CredentialsBachelor's degree, often some project management or clinical research experienceBachelor's degree, entry-level in clinical research
Work EnvironmentSupports project managers, involved in planning and oversightAssists with daily tasks, data collection, and site communication
Employer & Industry UsagePharmaceutical, biotech, clinical research organizationsClinical research sites, CROs, pharma companies

The Associate Clinical Project Manager typically has more responsibility in project planning and oversight compared to the Clinical Project Coordinator, who mainly supports data collection and site coordination. Both roles are essential in clinical research teams, with the associate role often serving as a stepping stone to more senior project management positions.

What are the most commonly searched types of Clinical Project Manager jobs in Arizona? The most popular types of Clinical Project Manager jobs in Arizona are:
What are popular job titles related to Associate Clinical Project Manager jobs in Arizona? For Associate Clinical Project Manager jobs in Arizona, the most frequently searched job titles are:
What job categories do people searching Associate Clinical Project Manager jobs in Arizona look for? The top searched job categories for Associate Clinical Project Manager jobs in Arizona are:
What cities in Arizona are hiring for Associate Clinical Project Manager jobs? Cities in Arizona with the most Associate Clinical Project Manager job openings:
Associate Clinical Project Manager jobs near you
Infographic showing various Associate Clinical Project Manager job openings in Arizona as of June 2026, with employment types broken down into 1% Locum Tenens, 1% As Needed, 74% Full Time, 22% Part Time, 1% Temporary, and 1% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $75,107 per year, or $36.1 per hour.
Associate Clinical Project Manager

Associate Clinical Project Manager

Becton, Dickinson and Company

Tempe, AZ • On-site

Full-time

Posted 23 days ago

BD rating

7.3

Company rating: 7.3 out of 10

Based on 135 frontline employees who took The Breakroom Quiz

249th of 417 rated machine equipment manufacturers

Job description

We are the people who give possibilities purpose
BD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it's no small feat. It takes the imagination and passion of all of us-from design and engineering to the manufacturing and marketing of our billions of MedTech products per year-to look at the impossible and find transformative solutions that turn dreams into possibilities.
Job Description
Job Responsibilities: (Primary Duties, Roles, and/or Authorities)
Under direct manager supervision, the Associate Clinical Project Manager will:
  • Manage the quality and compliance of assigned clinical project(s) ensuring that they meet the highest standards for scientific quality, integrity and ethics and are conducted in accordance with BD global clinical procedures, study protocols, GCP and all applicable regulations.

  • Plan and strategize with other business unit cross functional team members (R&D, Marketing, Quality, and other business partners) to define, implement and execute clinical strategies in support of business objectives.

  • Demonstrate a comprehensive understanding of the therapeutic areas and competitive landscapes for assigned clinical project(s).

  • Oversee the planning and execution of assigned clinical projects to ensure that deliverables are completed on time and within budget. Develop and manage metric reporting tools as needed to track project timelines and deliverables. Provide regular and ad hoc reporting of metrics to Clinical Affairs leadership.

  • Manage activities related to clinical strategy and study design, global applications, submissions, and product launches for assigned clinical project(s) as the clinical subject matter expert.

  • Develop Clinical Investigation Plans (CIPs), Informed Consent Forms (ICFs), Investigator's Brochure's (IBs), Clinical Study Management Plans, Study Process Risk Assessments, Regulatory Management Plans, Case Report Forms (CRFs), Clinical Product Management Plans, Clinical Investigation Reports (CIRs) and other essential clinical study documents.

  • Review and provide input on the development of other essential clinical study documents related to clinical data management, clinical statistics, site management & monitoring, clinical safety management, clinical product management and clinical supplier management.

  • Develop and manage clinical study budgets and monthly financial reviews, including invoice review/approval and accruals for assigned clinical project(s).

  • Manage compliance for required reporting, including but not limited to IDE annual reports, clinicaltrials.gov, and overseas notified bodies/competent authorities.

  • Perform study and/or site-level audits of the Trial Master File (TMF) to ensure that study files are current, accurate, complete and audit-ready.

  • Oversee study and site-level management of the Clinical Trial Management System (CTMS) to ensure that study and site details are current, accurate and complete.

  • Interact with and/or oversee interactions with investigational sites, vendors, key opinion leaders (KOLs) and consultants.

  • Manage external contractors/suppliers for assigned clinical project(s) to ensure that deliverables are completed on-time, within budget, and are consistent with the scope of work.

  • Coach and ensure successful and effective relationships between study teams and investigational site personnel.

  • Provide critical thinking and leadership support for issue escalation related to clinical study activities. Interact with investigational sites, vendors, and other functional areas for issues, as needed. Proactively identify issues and create mitigation strategies in collaboration with Clinical Affairs leadership.

  • Provide support for internal or external audits/inspections and ensure resolution of audit/inspection findings related to assigned clinical projects.

  • Conduct Site Management & Monitoring, Clinical Product Management and Clinical Field support activities/visits, as needed.

  • Conduct, attend, or support training and observational activities, as needed, for study team members.

Education and Experience:
  • Bachelor's Degree (BS/BA) in life sciences (MA/MS preferred)

  • 3+ years of experience in clinical research (medical device, pharmaceutical and/or biotechnology)

Knowledge and Skills:
Required Qualifications:
  • Knowledge of domestic and international clinical research regulations and guidelines, Good Clinical Practice (GCP) and current industry practices related to the conduct of clinical studies

  • Proficiency with Microsoft Suite tools (Outlook, Word, Excel, PowerPoint, OneNote, To-Do, SharePoint, etc.)

  • Strong knowledge of clinical study processes and systems (eTMF, CTMS and CDMS)

  • Strong interpersonal and communication (oral and written) skills

  • Strong organizational skills, attention to detail, critical thinking and analytical skills

  • Able to manage and delegate multiple tasks and prioritize importance of tasks/projects

  • Ability to understand and interpret technical, scientific, and clinical information as it applies to product approval activities

  • Ability to lead teams to translate issues into actions, make decisions and influence outcomes

  • Ability to travel up to 40% (or more during peak times)

Preferred Qualifications:
  • Prior experience with clinical studies related to peripheral vascular diseases, end-stage kidney disease and/or oncology

  • Prior experience managing clinical projects (strongly preferred)

  • Experience with medical device studies (strongly preferred)

  • Prior experience with site management & monitoring

  • Prior experience with Veeva Vault Clinical Suite (CTMS, CDMS and eTMF)

  • Professional certification through one or more relevant associations (e.g., ACRP, SOCRA, etc.)

Physical Demands: (if applicable)
While performing the duties of this job, the employee is regularly required to stand, walk, sit, use sight, and use hands to manipulate, handle or feel objects, tools, controls, and office equipment. The employee frequently is required to verbally communicate with other associates. The employee is occasionally required to reach with hands and arms and stoop, kneel or crouch.
Work Environment: (if applicable)
While performing the duties of this job, the employee may be in an open cubicle environment. Candidate must be able to work in a team-oriented, fast-paced environment. BD is an affirmative action, equal opportunity employer that values and actively seeks diversity in the workforce.
Why Join Us?
To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of healthcare. At BD, you'll discover a culture in which you can learn, grow and thrive.
We believe that when people connect in person, we learn faster, collaborate more deeply, and build a stronger culture. Join us and enjoy a culture where face-to-face collaboration supports your learning, your progress, and your success.
To learn more about BD visit https://bd.com/careers.
Becton, Dickinson, and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally protected characteristics.
Required Skills
Optional Skills
Primary Work Location
USA AZ - Tempe Headquarters
Additional Locations
Work Shift

What BD employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom

BD logo

About BD

Sourced by ZipRecruiter

BD is one of the largest global medical technology companies in the world and is advancing the world of health by improving medical discovery, diagnostics and the delivery of care. We have over 65,000 employees and a presence in virtually every country around the world to address some of the most challenging global health issues.

Industry

Medical equipment and supplies manufacturing and manufacturing

Company size

10,000+ Employees

Headquarters location

Franklin Lakes, NJ, US

Social media

FacebookTwitter

View All BD Jobs

Apply