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Live In Clinical Project Manager Jobs in Pennsylvania

The Project Manager is in constant communication with our Account Management team to understand and ... Review live websites, HTML files, and videos to confirm that they match approved versions REQUIRED ...

Senior Project Manager - Oncology Clinical Trials This role leads the end-to-end management of ... Support the Senior Director, Clinical Research in clinical trial management activities and ...

Partner with CRA's, Global Project Leads, and cross-functional teams to ensure successful study ... Proficiency in clinical systems (e.g., CTMS, eTMF) * 3-5+ years of total trial management ...

Partner with CRA's, Global Project Leads, and cross-functional teams to ensure successful study ... Proficiency in clinical systems (e.g., CTMS, eTMF) * 3-5+ years of total trial management ...

... drug supply management in clinical trials * Support the Services Delivery project team in ... Providing protocol-specific support to the client and support team after go-live * Ensure client ...

... drug supply management in clinical trials * Support the Services Delivery project team in ... Providing protocol-specific support to the client and support team after go-live * Ensure client ...

The Clinical Supply Manager is responsible for the successful execution of clinical supply projects ... in alignment with business capabilities. * Manage and oversee project execution and on-time ...

Showing results 41-60

Live In Clinical Project Manager information

What is a live in clinical project manager?

A Live In Clinical Project Manager is a professional responsible for overseeing and coordinating clinical trials or healthcare projects, often in a residential or on-site setting. Their duties typically involve managing study protocols, ensuring regulatory compliance, coordinating with medical staff, and monitoring patient safety and data quality. They may be required to live on-site or near the project location to provide around-the-clock support and leadership. This role is crucial for the smooth operation and success of clinical programs, especially those requiring continuous oversight.

How does a live in clinical project manager typically collaborate with clinical staff and external stakeholders during a clinical trial?

A Live In Clinical Project Manager works closely with on-site clinical staff, including nurses, physicians, and research coordinators, to ensure that trial protocols are followed accurately and patient safety is prioritized. They also act as the primary point of contact between the site and external stakeholders such as sponsors, regulatory bodies, and vendor partners. Regular meetings, detailed reporting, and transparent communication are key aspects of the collaboration, helping to address challenges quickly and keep the project on track. This role requires strong interpersonal skills and the ability to adapt to dynamic clinical environments.

What are the key skills and qualifications needed to thrive as a live in clinical project manager, and why are they important?

To thrive as a Live In Clinical Project Manager, you need strong project management skills, clinical research experience, and a relevant degree in life sciences or healthcare. Familiarity with clinical trial management systems (CTMS), regulatory compliance tools, and certifications like PMP or GCP are typically essential. Exceptional organizational, leadership, and communication skills help you coordinate teams and maintain effective stakeholder relationships. These skills ensure that clinical projects are executed efficiently, ethically, and within regulatory standards, ultimately safeguarding patient safety and study integrity.

What is the difference between Live In Clinical Project Manager vs Clinical Project Coordinator?

AspectLive In Clinical Project ManagerClinical Project Coordinator
CredentialsBachelor's degree in life sciences or related field; often PMP or similar certificationsBachelor's degree in health sciences or related field; certification is a plus
Work EnvironmentLeads clinical trials, manages teams, and oversees project progress on-site or remotelySupports project activities, coordinates schedules, and assists managers
Employer & IndustryPharmaceutical companies, CROs, biotech firmsResearch organizations, hospitals, clinical research sites

The Live In Clinical Project Manager typically holds more responsibilities, including leading clinical trials and managing teams, often requiring certifications like PMP. The Clinical Project Coordinator focuses on supporting project tasks and coordination. Both roles are essential in clinical research but differ in scope and seniority.

What are the most commonly searched types of Clinical Project Manager jobs in Pennsylvania?

The most popular types of Clinical Project Manager jobs in Pennsylvania are:

What cities in Pennsylvania are hiring for Live In Clinical Project Manager jobs?

Cities in Pennsylvania with the most Live In Clinical Project Manager job openings:

Project Manager, LIVE

WebMD

Yardley, PA

Full-time

Posted 27 days ago


Job description

MedscapeLIVE!, a Medscape Company, delivers MD and HCP audiences across all therapeutic areas. Access MDs and HCPs through MedscapeLIVE! Events.
WebMD is an Equal Opportunity/Affirmative Action employer and does not discriminate on the basis of race, ancestry, color, religion, sex, gender, age, marital status, sexual orientation, gender identity, national origin, medical condition, disability, veterans status, or any other basis protected by law.

SUMMARY:

The Project Manager will lead Medscape's broadcasts projects through the Medical/Legal/Regulatory (MLR) process from sale to launch. This role requires a highly detail-oriented individual that wants to take a hands-on approach in a fast-paced and deadline-driven environment. Day-to-day responsibilities include preparing and editing content submissions for multiple projects, thorough QC of submission materials, tracking project progress, and monitoring timelines. The Project Manager is in constant communication with our Account Management team to understand and meet the needs of our clients and daily correspondence with other internal teams to revise and produce our images, websites, videos, and other digital work.

ESSENTIAL DUTIES AND RESPONSIBILITIES include, but are not limited to, the following:

  • Successfully manage projects from sale to launch

  • Prepare/edit documents required for submission and approval through various pharmaceutical regulatory processes

  • Thorough editorial and correctness QC of all submission materials

  • Coordinate with Account, Creative, Technology, and Event teams in the execution of projects

  • Serve as primary point of contact for project-related requests

  • Manage timelines for all project deliverables

  • Use project management software to track projects and provide frequent status updates

  • Use online submissions systems to upload pieces, download comments, tag references, and track progress

  • Interpret and address Medical/Legal/Regulatory comments

  • Review live websites, HTML files, and videos to confirm that they match approved versions

REQUIRED EDUCATION AND EXPERIENCE:

  • Minimum of 1-2 years of experience in pharmaceutical advertising or equivalent fast-paced environment

  • Must have solid Microsoft Office experience especially related to Word, Excel, and Outlook

  • Knowledge of Adobe InDesign and project management software a plus

KNOWLEDGE, SKILLS AND ABILITIES:

  • Strong organizational, analytical skills, and strong attention to detail

  • Proven ability to multitask, adjust priorities, meet deadlines, and successfully operate in a fast-paced work environment

  • Ability to follow through on and successfully execute tasks while adhering to specified quality standards

  • Excellent problem analysis, troubleshooting, problem-solving and decision-making skills

  • Possess proactive mindset to seek information to create effective solutions

  • Proven ability to build rapport while providing superior service and maintaining positive relationships with internal teams and external vendors/contacts

  • Ability to work well independently and as a team member

  • Excellent interpersonal, verbal, and written communication skills

  • Have a good understanding of how to motivate people and to get to the heart of the matter

  • Must have a professional attitude and be able to deal effectively with all levels of the organization

  • Possess a high comfort level with technology, technical processes, and digital materials

Employment Type: Full-Time