1,000+ matching jobs for “Specialist - Collaboration”

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Palo Alto Networks

Senior Events Specialist

Office - USA - CA - Headquarters

We're looking for a Senior Events Specialist to join our Global Events team. This is an exciting opportunity for a highly organized, creative, and …

Added Oct 27, 2026

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Booz Allen Hamilton

International Security Specialist

Arlington, Virginia, United States

Pay posted by employer$53,000–$108,000

International Security Specialist The Opportunity: Maintain responsibility for coordinating security planning for foreign participation, …

Added Oct 27, 2026

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Booz Allen Hamilton

International Security Specialist

Arlington, Virginia, United States

Pay posted by employer$69,400–$158,000

International Security Specialist The Opportunity: Maintain oversight for coordinating security planning for foreign participation, …

Added Oct 27, 2026

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S&P Global

Commercial Specialist- Chemicals

Beijing, Beijing, China +1 location

Full time

Grade Level (for internal use): 11 The Team: The APAC Specialist team comprises dynamic professionals with deep commodity expertise, many bringing industry backgrounds as …

Added Oct 27, 2026

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Becton Dickinson

Clinical Safety Specialist

USA AZ - Tempe Headquarters

In person
Full time
Regular

Job Summary: The Clinical Safety Specialist is responsible for delivering high quality and compliant Clinical Safety management for clinical studies …

Added Oct 27, 2026

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Booz Allen Hamilton

Operations Research Specialist

Honolulu, Hawaii, United States

Pay posted by employer$86,900–$198,000

Operations Research Specialist The Opportunity: As an expert in defense missions, your unique background inspires you to think bigger, …

Added Oct 31, 2026

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TD Synnex

Freight excellence specialist

Barcelona, Catalonia, Spain

Full time
Regular

… What we offer: 🏡 Hybrid Work Model – Combine the flexibility of remote work with the benefits of in-person collaboration (2 days in the office, 3 days from home). 🛡️ Life Insurance – Comprehensive coverage through Generali, …

Added Oct 27, 2026

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GE HealthCare Technologies

Clinical Imaging Specialist

Remote

Pay posted by employer$105,840–$158,760

Summary As a Clinical Imaging Specialist, you will utilize your clinical expertise to support the market leader in surgical C-arms. You will …

Added Oct 27, 2026

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Booz Allen Hamilton

Workday HCM Specialist

McLean, Virginia, United States

Pay posted by employer$77,600–$176,000

Workday HCM Specialist The Opportunity: Spearhead the configuration and optimization of Workday business processes, lead special …

Added Oct 27, 2026

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Booz Allen Hamilton

Personnel Security Specialist

Naples, Campania, Italy

Pay posted by employer$77,500–$176,000

Personnel Security Specialist The Opportunity: Process and maintain company and government inspectable records and procedures for …

Added Oct 27, 2026

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Booz Allen Hamilton

Cyber Compliance Specialist

Arlington, Virginia, United States

Pay posted by employer$62,000–$141,000

Cyber Compliance Specialist The Opportunity: Design, implement, and manage policies and procedures to ensure database and sof tware …

Added Oct 27, 2026

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Booz Allen Hamilton

Strategic Engagement Specialist

Dededo, Guam

Pay posted by employer$86,800–$198,000

… unless permission is explicitly provided . Work Model Our people-first culture prioritizes the benefits of collaboration. To support engagement and effective communication, employees working virtually are generally expected to …

Added Oct 27, 2026

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Booz Allen Hamilton

Organizational Change Specialist

Arlington, Virginia, United States

Pay posted by employer$77,600–$176,000

Organizational Change Specialist The Opportunity: Whether it’s process improvement, performance measurement, or business management analysis …

Added Oct 27, 2026

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Booz Allen Hamilton

CRM Program Specialist

McLean, Virginia, United States

Pay posted by employer$86,800–$198,000

CRM Program Specialist The Opportunity: Drive the adoption of the company’s opportunity pipeline and customer relationship …

Added Oct 27, 2026

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Booz Allen Hamilton

Operations Research Specialist

Honolulu, Hawaii, United States

Pay posted by employer$86,900–$198,000

Operations Research Specialist The Opportunity: As an expert in defense missions, your unique background inspires you to think bigger, …

Added Oct 27, 2026

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Gilead Sciences

Specialist, Quality Assurance

Tokyo, Japan

Full time
Regular

We are seeking a highly motivated individual to join us as Specialist for Japan. You will work in the Quality as one of the members of Tech.Ops and collaborate with Commercial …

Added Oct 15, 2026

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Dow

Rotating Equipment Specialist

Knoxville (TN, USA)

In person
Full time
Regular

Added Oct 27, 2026

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GE HealthCare Technologies

Service Sales Specialist

AUS08-01-Sydney-241 O'Riordan Street, 8F

Summary As a Service Sales Specialist, you will play a pivotal role in driving revenue growth through the sale of Maintenance Service Agreements …

Added Oct 27, 2026

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Dow

Customer Service Specialist

Navi Mumbai, Maharashtra, India

In person
Full time
Regular

… Excellent verbal and written communication skills. Effective stakeholder management and cross-functional collaboration. Strong analytical and problem-solving capabilities. Ability to make sound business decisions in a …

Added Oct 27, 2026

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Bristol-Myers Squibb

Specialist, QC Microbiology

Leiden – NL

Full time
Temporary

… perfectly match your resume, we encourage you to apply anyway. How We Work Where you work matters – because collaboration, innovation and patient impact happen in many settings. Our roles are structured across four work models: …

Added Oct 15, 2026

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Becton Dickinson

Clinical Safety Specialist

USA AZ - Tempe Headquarters

In person
Full time
Regular

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Required Qualifications · employer excerpt

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

2 more in the full description below.

About this opportunity

Original employer 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

Optional Skills

Primary Work LocationUSA AZ - Tempe Headquarters

Additional Locations

Work Shift

Why this result? · Employer labels

Keywords also found in description

Full time
Medical / Clinical Affairs
Onsite
Regular

Location reference: GeoNames (CC BY 4.0), normalized by Referizz.