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Remote Pharmaceutical Data Management Jobs in Rochester, NY

Customer Success Management * Build trusted relationships with customer stakeholders and executive ... Monitor SIM usage, data consumption, and service trends. * Coordinate operational requests with ...

... Remote Sim Provisioning (RSP), SGP02, and SGP22. * Strong project and time management skills ... Ability to take on and manage projects with a can-do attitude. * Ability to analyze data and ...

Social Media Managers 2026

Rochester, NY ยท On-site +1

$3.9K/mo

Hybrid (Remote/Office) | Global About the Role: Google is looking for a passionate and results ... Analyze campaign performance data to identify insights and refine strategies for continuous ...

... management of assigned therapists when necessary * Perform ongoing review of high-risk cases and ... If you would like more information about how your data is processed, please contact us.

This role is based in United State and is a remote position. You will be part of a collaborative ... Analyze process and laboratory data to identify improvement opportunities and make recommendations

Remote micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety ... Author and review evaluation tasks based on DSURs, PSURs/PBRERs, and associated safety data and ...

Pharmacovigilance Expert

Rochester, NY ยท Remote

$70 - $80/hr

Remote micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety ... Author and review evaluation tasks based on DSURs, PSURs/PBRERs, and associated safety data and ...

FP&A Manager - AI Trainer

Rochester, NY ยท Remote

$50 - $100/hr

Enjoy the flexibility of remote work and the freedom to set your own schedule. This is an ... modeling, data analysis, and other reasoning exercises related to finance management * A current ...

Showing results 41-60

Remote Pharmaceutical Data Management information

What is remote pharmaceutical data management?

Remote pharmaceutical data management involves overseeing, organizing, and maintaining pharmaceutical data from a location outside of a traditional office or laboratory setting. Professionals in this field manage clinical trial data, drug information, and compliance records using specialized software and secure cloud systems. The role is essential for ensuring data accuracy, integrity, and accessibility, which supports regulatory submissions and decision-making in pharmaceutical research. Remote positions allow for flexibility while still maintaining strict data security and confidentiality standards.

What are the key skills and qualifications needed to thrive in remote pharmaceutical data management?

To thrive in Remote Pharmaceutical Data Management, you need strong analytical skills, knowledge of pharmaceutical regulations, and a degree in life sciences or a related field. Familiarity with data management systems like Medidata Rave, CDISC standards, and GCP certification is highly valuable. Attention to detail, effective communication, and problem-solving abilities help professionals excel in remote collaboration and data integrity. These skills ensure accurate, compliant data handling crucial for clinical trial success and regulatory approval.

How does a remote pharmaceutical data management professional typically collaborate with cross-functional teams?

Remote pharmaceutical data management professionals frequently work with clinical research, regulatory, and IT teams to ensure data integrity and compliance. Collaboration is often facilitated through virtual meetings, secure data-sharing platforms, and project management tools, allowing seamless communication despite physical distance. Regular updates and coordinated timelines are essential to align data processes with broader project goals. This collaborative approach not only supports accurate data management but also enhances overall project efficiency and regulatory compliance.

What is the difference between Remote Pharmaceutical Data Management vs Remote Clinical Data Coordinator?

AspectRemote Pharmaceutical Data ManagementRemote Clinical Data Coordinator
CredentialsBachelor's in Life Sciences, Data Management certificationsBachelor's in Health Sciences, Data Entry certifications
Work EnvironmentPharmaceutical companies, CROs, biotech firmsClinical trial sites, research organizations
Industry UsageData handling, compliance, database managementData collection, entry, and validation in clinical trials

Remote Pharmaceutical Data Management involves overseeing and maintaining pharmaceutical data, ensuring compliance and accuracy, often in a corporate or research setting. In contrast, Remote Clinical Data Coordinators focus on collecting and validating clinical trial data at research sites. Both roles require strong data skills but differ in their specific responsibilities and work environments.

What job categories do people searching Remote Pharmaceutical Data Management jobs in Rochester, NY look for?

The top searched job categories for Remote Pharmaceutical Data Management jobs in Rochester, NY are:

What cities near Rochester, NY are hiring for Remote Pharmaceutical Data Management jobs?

Cities near Rochester, NY with the most Remote Pharmaceutical Data Management job openings:

Infographic showing various Remote Pharmaceutical Data Management job openings in Rochester, NY as of August 2026, with employment types broken down into 56% Full Time, 23% Part Time, 5% Temporary, and 16% Contract. Highlights an 100% Remote job distribution.

Project Manager, Imaging and Cardiac

410 ICR United States USA

Rochester, NY โ€ข Remote

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 4 days ago


Job description

Project Manager, Imaging and Cardiac

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.


As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.


Location: Remote

Overall Job Summary:

The Project Manager is the main point of contact for customers on all assigned projects and acts as the lead on a portfolio of clinical trials within ICON Medical Imaging and Cardiac Safety Solutions team. The Project Manager will act as primary point of contact for customer communication, managing routine teleconferences and reporting deliverables. The Project Manager is responsible for developing project timelines, assure adherence to the timelines, and provide customer support throughout the life cycle of a project for all study-related activities within a clinical trial. This position will coordinate cross-functional activities of internal resources to ensure quality and on-time project deliverables are met.  The Project Manager is responsible for maintaining the proper project documentation and ensuring compliance with SOPs and regulatory requirements for clinical trials. The Project Manager will be responsible for revenue forecasting, tracking, and submittal, and will also update budgets and contracts as necessary.

Essential Responsibilities:

  • Apply project management principles, concepts and techniques for effective project management, including quality assurance and customer satisfaction
  • Maintain a positive, results-oriented work environment by building partnerships, modeling teamwork and communicating in an open, balanced and objective manner
  • Act as the primary contact and study lead with the customer from startup through close-out of a project with minimal supervision and oversight
  • Develop and implement project plans and timelines via internal and external kick-off meetings and ensure agreement by parties involved, with minimal supervision
  • Develop presentations for Investigator Meetings and customer facing meetings and travel independently to present at these meetings when required
  • Escalate issues to management as appropriate
  • Complete revenue, forecasting and invoicing per process on-time and accurately
  • Coordinate cross-functional teams to ensure efficient processing of project requirements, with minimal support
  • Conduct routine customer teleconferences and generate and maintain accurate records and meeting minutes and agendas in accordance with regulatory guidelines
  • Update budgets and contracts and gain management approvals for Change Requests
  • Generate and maintain Patient and Site Tracking Reports via MS Excel and study databases and provide updates to customers on a regular basis
  • Coordinate with internal teams to query sites to submit incoming data and resolve data issues
  • Travel with Business Development for customer meetings, as requested
  • Present internally and externally on project portfolio
  • Identify potential risks to projects and implement processes and tactics to proactively mitigate
  • Compliance with internal SOPs and WIs
  • Participate in developing and updating internal documents and guides (e.g. training materials, SOPs, etc.)
  • Participate, as requested by Regulatory Affairs, in customer audits
  • Provide oversight of Site Management and Reader Management activities for assigned projects
  • Meet or exceed internal Project Management metrics
  • Travel possibly required up to 20% of the time 

Education and Experience Requirements:

  • Education:  Minimum Bachelor’s Degree (preference in Life Sciences or similar) or equivalent education/work experience
  • Relevant Work Experience:  Required minimum of three years in a customer-focused role. Desired minimum of one year working in a project management role within the clinical trial industry. Imaging or Cardiac experience preferred but not required.    
  • Language: Advanced English fluency required for business communication. Previous work history in English as primary language required.

#LI-SB7

#LI-Remote


Employment with ICON is contingent upon having the legal right to work in the country where the role is based.


Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.


Benefits may include:

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.


Visit our careers site to read more about the benefits ICON offers.


Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.


If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

Are you a current ICON Employee? Please click here to apply