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Dmc Jobs in Gilbert, AZ (NOW HIRING)

PRA Business Events

Event Producer

Phoenix, AZ · On-site

We're PRA, the leading destination management company (DMC) with 45+ years of experience across 32+ states and 100+ destinations.We believe destinations have power-and our people unlock its magic. We ...

Desert Mountain

Cook II (Full-Time)

Scottsdale, AZ · On-site

$21/hr

Execute all duties in accordance of DMC, Servsafe, and health department standards. * Maintain walk-in coolers and food storage areas on a daily basis. * Other duties as assigned by management.

PRA

Event Producer

Phoenix, AZ · Hybrid

We're PRA, the leading destination management company (DMC) with 45+ years of experience across 32+ states and 100+ destinations. We believe destinations have power-and our people unlock its magic.

PRA Business Events

Event Producer

Phoenix, AZ · On-site

We're PRA, the leading destination management company (DMC) with 45+ years of experience across 32+ states and 100+ destinations. We believe destinations have power-and our people unlock its magic.

Desert Mountain

Cook III

Scottsdale, AZ · On-site

$17.25 - $21.25/hr

Ensure food meets the quality, taste, and appearance standards of DMC. * Check and complete mise en place and pars to set-up the station. * Maintain a working knowledge of properly storing, rotating ...

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Dmc information

See Gilbert, AZ salary details

$30.9K

$56K

$97.7K

How much do dmc jobs pay per year?

As of Aug 31, 2026, the average yearly pay for dmc in Gilbert, AZ is $55,952.00, according to ZipRecruiter salary data. Most workers in this role earn between $42,700.00 and $63,800.00 per year, depending on experience, location, and employer.

What is a dmc?

DMC stands for Destination Management Company. DMCs are professional service companies that specialize in organizing and coordinating events, activities, tours, transportation, and program logistics in a specific destination. They work with corporate clients, event planners, and travel agencies to provide local expertise and ensure smooth, memorable experiences tailored to the needs of the group. DMCs leverage their local knowledge, supplier relationships, and logistical experience to deliver high-quality, customized services for meetings, incentives, conferences, and events.

What are some common challenges faced by Destination Management Consultants when organizing large-scale events, and how can they be addressed?

Destination Management Consultants often encounter challenges such as coordinating with multiple local vendors, managing tight timelines, and ensuring seamless logistics for large groups. Effective communication, thorough planning, and building strong relationships with trusted suppliers are crucial for overcoming these hurdles. Additionally, staying flexible and having contingency plans in place helps DMCs quickly adapt to unexpected changes, ensuring successful event execution.

What are the key skills and qualifications needed to thrive as a Data Management Coordinator, and why are they important?

To thrive as a Data Management Coordinator, you need strong analytical skills, attention to detail, and a background in data management or related fields, often supported by a relevant degree. Familiarity with data management systems, database software (such as SQL), and sometimes certifications like CDMP (Certified Data Management Professional) are typically required. Excellent organization, problem-solving, and communication skills help you collaborate effectively with teams and maintain data accuracy. These competencies are crucial for ensuring data integrity, compliance, and efficient information flow within organizations.

What is the difference between Dmc vs Mdc?

AspectDmcMdc
CredentialsTypically requires certification in distribution or supply chain managementOften requires similar certifications, with additional focus on medical or technical knowledge
Work EnvironmentWarehouse, distribution centers, logistics hubsMedical facilities, healthcare settings, or technical environments
Employer & IndustryLogistics companies, retail, manufacturingHealthcare providers, medical device companies, hospitals

While both Dmc and Mdc roles involve distribution and management, Dmc primarily focuses on logistics and supply chain operations in retail or manufacturing sectors. Mdc roles are more specialized in medical or technical environments, often requiring additional certifications. Understanding these differences helps in choosing the right career path or job search focus.

What cities near Gilbert, AZ are hiring for Dmc jobs?

Cities near Gilbert, AZ with the most Dmc job openings:

Dmc jobs near you
Infographic showing various Dmc job openings in Gilbert, AZ as of August 2026, with employment types broken down into 3% As Needed, 84% Full Time, 12% Part Time, and 1% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $55,952 per year, or $26.9 per hour.

Clinical Safety Specialist

Becton, Dickinson and Company

Tempe, AZ • On-site

Full-time

Posted 19 days ago

BD rating

7.3

Company rating: 7.3 out of 10

Based on 143 frontline employees who took The Breakroom Quiz

312th of 495 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 Summary:
The Clinical Safety Specialist is responsible for delivering high quality and compliant Clinical Safety management for clinical studies (e.g., EFS/FIH, IDE, Post-Market) sponsored by the BD Peripheral Intervention business unit to ensure 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.
Key Job Responsibilities:
  • Provide Clinical Safety Management support for BDPI clinical studies to enable successful completion of study objectives and deliverables.
  • Ensure quality and compliance for safety-related activities performed for assigned clinical studies.
  • Conduct Clinical Safety monitoring activities for assigned clinical studies to proactively identify/review/track reportable safety events, identify safety event trends/signals, issue and address data queries, ensure timely reporting for reportable safety events (e.g., Unanticipated Adverse Device Effects, device deficiencies, etc.), address/escalate safety non-compliance issues, and verify that any corrective actions are implemented.
  • Serve as the Clinical Safety expert and resource for BD stakeholders, Investigators, and study site personnel for assigned clinical studies.
  • Develop and maintain strong relationships with investigational site staff, HCP consultants (e.g., Medical Monitors, CEC/DMC members), and cross-functional study teams to support Clinical Safety deliverables. Facilitate communication between clinical sites and BD stakeholders (e.g., PMs, CRAs), as needed.
  • Develop and manage study-specific tracking reports for Clinical Safety, as needed, to ensure Clinical Safety reporting is completed compliantly and that other Clinical Safety deliverables are completed within study-specific timelines and budgets for assigned clinical studies. Provide regular Clinical Safety status updates to relevant BD and study stakeholders.
  • Perform study and/or site-level audits of the Trial Master File (TMF) to ensure that Clinical Safety related study files are current, accurate, complete and audit-ready.
  • Develop and/or complete study-specific Clinical Safety Plans, Medical Monitor Approval Forms, Clinical Events Committee (CEC) Charters, Data Monitoring Committee (DMC) Charters, Sponsor Assessment of Event Templates, Potential U(S)ADE/Serious Health Threat Assessment Forms, Preliminary Clinical Safety Threshold Evaluation Forms, Safety Event Narratives, Financial Disclosure Forms, Potential Conflict of Interest Forms, Requests for Clinical Supplier Contract Forms, Study Training Records, Clinical Non-Compliance Escalation Forms and other essential clinical safety-related study documents, as needed.
  • Review and provide input on the development of other essential clinical study documents related to Clinical Project Management, Site Management & Monitoring, Clinical Data Management, Clinical Statistics, Clinical Product Management and Clinical Supplier Management.
  • Report and escalate BD product complaints and other events/issues that inhibit safe and effective use of BD products and negatively impact data collection and study performance to BD stakeholders in accordance with established clinical study procedures, regulations and company policies.
  • Manage safety-related interactions, training and invoicing for Medical Monitors, CEC Members, DMC Members and other Clinical Safety vendors.
  • Participate in, support and/or lead study-specific meetings including, but not limited to Safety Event Trending Meetings, CEC Adjudication/Meetings, DMC Meetings, safety-related study team meetings, and vendor meetings.
  • Provide critical thinking and support for issue escalation related to Clinical Safety. Interact with investigational sites, vendors, and other functional areas for issues, as needed. Proactively identify issues and create mitigation strategies in collaboration with Clinical Project Management and other leadership.
  • Provide support for internal or external audits/inspections and ensure resolution of audit/inspection findings related to Clinical Safety activities.
  • Support continuous improvement activities/initiatives and sharing of best practices, including development of Clinical Safety tools and resources.
  • Mentor Clinical Safety personnel and conduct evaluations for other Clinical Safety personnel, as needed. Identify performance issues and training opportunities and communicate with Clinical Safety leadership, as needed.

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.)
  • Proficient knowledge of clinical study processes and systems (eTMF, CTMS and CDMS)
  • Strong interpersonal and communication/presentation (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 travel up to 10% (or more during peak times)

Preferred Qualifications:
  • Prior experience with clinical studies related to peripheral vascular diseases, end-stage kidney disease and/or oncology
  • Experience with medical device studies
  • Proficiency with Veeva Vault CTMS, CDMS and eTMF
  • Professional certification through one or more relevant associations (e.g., ACRP, SOCRA, etc.)

Education and Experience:
  • Bachelor's Degree (BS/BA) in life sciences, nursing, a related healthcare field equivalent OR a related certification in cardiology or radiology or equivalent combination of training and experience (MA/MS preferred)
  • 2+ years of experience in clinical research (medical device, pharmaceutical and/or biotechnology)
  • 2+ years of experience with clinical safety management or medical device safety reporting

At BD, we prioritize on-site collaboration because we believe it fosters creativity, innovation, and effective problem-solving, which are essential in the fast-paced healthcare industry. For most roles, we require a minimum of 4 days of in-office presence per week to maintain our culture of excellence and ensure smooth operations, while also recognizing the importance of flexibility and work-life balance. Remote or field-based positions will have different workplace arrangements which will be indicated in the job posting.
For certain roles at BD, employment is contingent upon the Company's receipt of sufficient proof that you are fully vaccinated against COVID-19. In some locations, testing for COVID-19 may be available and/or required. Consistent with BD's Workplace Accommodations Policy, requests for accommodation will be considered pursuant to applicable law.
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
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Primary Work Location
USA AZ - Tempe Headquarters
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About BD

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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

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