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Director Clinical Project Management Jobs in Wisconsin

WI ยท On-site

$140 - $200/hr

Explore our careers.Director, Clinical Insights page is loaded## Director, Clinical ... Coordinate and manage project workflow for IntrinsiQ's Clinical Insights offerings, such as ...

WI ยท On-site

$100 - $140/hr

Assume the manager role on the inpatient units in a clinical capacity as needed. * Assist managers ... Participate in RBH committees, meetings, and team projects. * Demonstrate punctuality and ...

Implementation of design and content into content management tool * Attention to detail in quality ... Develop strong relationships with clinical study sponsors, clinical research organizations and ...

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Director Clinical Project Management information

What does a director of clinical project management do?

A Director of Clinical Project Management oversees the planning, execution, and completion of clinical trials within a pharmaceutical or biotech company. They lead project management teams, ensure regulatory compliance, manage budgets and timelines, and coordinate communication among stakeholders. Their responsibilities also include risk management, resource allocation, and ensuring trials meet both scientific and business objectives. This role is critical for bringing new medical treatments through the development pipeline to market approval.

What are some common challenges faced by a director of clinical project management, and how can they be addressed?

Directors of Clinical Project Management often encounter challenges such as managing complex, multi-site trials, maintaining regulatory compliance, and coordinating cross-functional teams. Balancing timelines, budgets, and quality expectations can also be demanding, especially when unexpected issues arise. Successful directors address these challenges by fostering clear communication, utilizing robust project management tools, and building strong relationships with stakeholders. Staying current with regulatory changes and providing mentorship to team members also helps ensure project success and professional growth.

What are the key skills and qualifications needed to thrive as a director of clinical project management, and why are they important?

To thrive as a Director of Clinical Project Management, you need deep expertise in clinical research, regulatory compliance, project leadership, and typically an advanced degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and certifications such as PMP or CCRP are commonly required. Strong strategic thinking, communication, and team leadership skills help drive project success and foster collaboration among cross-functional teams. These competencies are vital for delivering clinical trials on time, within budget, and in compliance with regulatory standards.

What is the difference between Director Clinical Project Management vs Clinical Project Manager?

AspectDirector Clinical Project ManagementClinical Project Manager
ResponsibilitiesOversees multiple projects, strategic planning, team leadershipManages individual clinical trials, day-to-day operations
Experience & CredentialsTypically requires 8+ years, advanced degrees, leadership experienceUsually 3-5 years, relevant clinical or project management certifications
Work EnvironmentSenior management, cross-functional teams, strategic meetingsProject teams, site coordination, operational tasks

The main difference is that the Director Clinical Project Management holds a senior leadership role overseeing multiple projects and strategic initiatives, while the Clinical Project Manager focuses on managing individual clinical trials and operational activities. Both roles require relevant experience and certifications, but the director's scope is broader and more strategic.

How much do director clinical project managements earn?

The salary for a Director of Clinical Project Management typically ranges from $120,000 to $180,000 annually, depending on experience, location, and the size of the organization. Senior roles with extensive experience and certifications like PMP or PMI-ACP can earn higher compensation, often including bonuses and benefits.

What are popular job titles related to Director Clinical Project Management jobs in Wisconsin?

For Director Clinical Project Management jobs in Wisconsin, the most frequently searched job titles are:

What job categories do people searching Director Clinical Project Management jobs in Wisconsin look for?

The top searched job categories for Director Clinical Project Management jobs in Wisconsin are:

What cities in Wisconsin are hiring for Director Clinical Project Management jobs?

Cities in Wisconsin with the most Director Clinical Project Management job openings:

Director, Clinical Insights

World Courier

WI โ€ข On-site

$140 - $200/hr

Other

Posted 7 days ago


Job description

Director, Clinical InsightsSkip to main contentWe use cookies and tracking technologies to offer you a better browsing experience, analyze site traffic, and improve the website.# AmerisourceBergen is now Cencora! Explore our careers.Director, Clinical Insights page is loaded## Director, Clinical InsightsApplylocations: Remote, Texastime type: Full timeposted on: Posted Todayjob requisition id: R269820Our team members are at the heart of everything we do. At Cencora, we are united in our responsibility to create healthier futures, and every person here is essential to us being able to deliver on that purpose. If you want to make a difference at the center of health, come join our innovative company and help us improve the lives of people and animals everywhere. Apply today!# **Job Details**The Director, Clinical Insights is primarily responsible for utilizing their clinical experience and expertise to manage HCP and pharmaceutical client-facing programs to ensure business requirements and deliverables are met with high quality related to clinical insight offerings.**Responsibilities*** Coordinate and manage project workflow for IntrinsiQโ€™s Clinical Insights offerings, such as specialty provider working groups, clinical impact programs, advisory boards, and clinical contracts* Serves as clinical liaison between pharmaceutical sponsors and internal stakeholders to ensure smooth execution of programs and deliverables* Provide clinical expertise and direction with Clinical Insights offerings* Develop and maintain relationships with key opinion leaders in the field of oncology, urology, retina and other specialties* Develop discussion guide in coordination with pharmaceutical sponsors and moderate working group engagements with specialty providers* Work closely with working group chairman to support direction and execution of group initiatives in collaboration with internal and external stakeholders* Lead the development and delivery of final data reports, executive summaries, and client presentations resulting from Clinical Insights programs* Collaborate with IQSS and Cencora business development account leads to identify sales opportunities and prepare proposals* Recognize changes in project scope, taking appropriate action with internal team members and the client* Demonstrate key knowledge of team projects: clients, business issue(s) objectives, scopes, budgets and timelines* Demonstrate understanding of Cencora solutions to execute projects* Seek and use customer feedback to improve processes and solutions* Adheres to all relevant SOPs and company policies regarding compliance, contracting and ethical firewalls* Maintain a safe, secure, and legal work environment.* Seek and develop personal growth opportunities* Performs other related duties as assigned**Education and Work Experience*** Experience in clinical oncology (RN, APP, PharmD) with strong oncology background and/or other specialty experience preferred. Experience in pharmaceutical industry/consulting in addition to clinical oncology setting a plus.* Additional specialty certification highly desired.* Completion of a four-year bachelorโ€™s degree program or equivalent combination of experience and education. Normally requires a minimum of 8+ years progressively responsible related experience**Skills and Knowledge*** Possesses and applies comprehensive knowledge of particular field of specialization to the completion of significant assignments. Crosses fields. Assignments necessitate advanced knowledge, sufficient to teach others* Experience in the development and implementation of healthcare provider-based programs.* Well-developed interpersonal and verbal and written communication skills.* Experience in medical writing and presentation of scientific/clinical/technical information.* Good interpersonal and relationship building skills* Good oral communication skills* Good written communication skills* Good group presentation skills, including capability presentations to prospects with good virtual-based/on-camera presence* Good analytical skills* Good organizational skills* Computer software: Excel, Word, PowerPoint* Demonstrated ability to work within teams and across teams* Strong knowledge of pharmaceutical industry, with demonstrated success in the industry or consulting to the industry* Demonstrated ability to perform roles/responsibilities independently and with sound judgment* Strong ability to work independently in remote-based environment* Ability to travel approximately 5-10 times/year #J-18808-Ljbffr