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Clinical Project Management Director, Internal Medicine


This is a Full-time position in Parsippany, NJ posted January 10, 2021.

n n nClinical Project Management Director, Internal Medicinen nn Durham, North Carolina, United States of America nn nn Overland Park, KS (QLEX, Home-based) nn nn New York, NY (NYC4, Home-Based) nn nn Atlanta, GA (QATL, Home-based) nn nn Cambridge, MA (QCBG, Home-based) nn nn Houston, TX (QHOU, Home-based) nn nn Philadelphia, PA nn nn Chicago, IL (CHI1, Home-Based, Mudra) nn nn Austin, Texas, United States of America nn nn PURPOSE nn nn nDirect and manage large, global, multi functional projects or program, including the execution of the clinical component of the project/program to the Sponsor’s satisfaction, ensuring quality deliverables, on time delivery and within budget.

Has strategic decision-making responsibility for the project/program.

Ensure that all project work is completed in accordance with SOPs, policies and practices.nn nn RESPONSIBILITIES nn nnManage the scope of work, objectives, quality of deliverables, and other project and study management activities.nn nnServe as primary project/program contact with Sponsor to ensure appropriate communication channels are maintained and reporting schedules adhered to.nn nnEnsure the development of project plans for all phases of the project lifecycle, including the quality and risk management, ensuring that issue escalation and resolution is clear.nn nnDevelop proactive contingency plans to mitigate clinical risk across studies.nn nnWork with Business Development to finalize the project/program budget and scope of work.nn nnDirect and lead project activities for team members related to their project-oriented tasks to ensure that project/program milestones are met.nn nnContinually review and make recommendations to ensure adequate resources are available to meet project deliverables and milestonesnn nnDevelop, lead and implement continuous improvement for assigned projects and programs.nn nnAct as the key relationship manager for assigned clients; recommend courses of action regarding client management issues; implement plan following approval by senior management.nn nnEnsuring adherence to change control processes.nn nnProvide consultation to clients on drug development process, study management strategy, and plans as needed.nn nnParticipate in proposal and budget development, evaluate feasibility of potential programs and impact on company operations and goals, negotiate and make decisions on behalf of the organization.

Participate in sales/proposal presentations in face-to-face meetings with potential clients.nn nnParticipate in function and/or corporate initiatives, special project assignments, and as a client liaison or departmental cross-functional liaison.nn nn REQUIRED KNOWLEDGE, SKILLS AND ABILITIES nn nnIn depth technical and/or therapeutic expertise and knowledge of study, project and drug development processesnn nnDemonstrated financial management skills, including project financial tracking and accounting methodsnn nnIn depth knowledge of, and skill in applying, applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelinesnn nnExcellent communication and interpersonal skills, including good command of English languagenn nnExcellent organization and problem-solving skillsnn nnAbility to balance operational and strategic prioritiesnn nnProven ability to work through others to deliver results to the appropriate quality and timeline metricsnn nnStrong influencing and negotiation skillsnn nnHighly effective team leadership skillsnn nnSound judgment and decision making skillsnn nnStrong software and computer skills, including MS Office applicationsnn nnAbility to establish and maintain effective working relationships with coworkers, managers and clients.nn nn MINIMUM REQUIRED EDUCATION AND EXPERIENCE nn nnBachelor’s degree in life sciences or related field and 12 years clinical research experience including 8 years project management/ leadership experience, including multi-regional and global focus; or equivalent combination of education, training and experiencenn nn PHYSICAL REQUIREMENTS nn nnExtensive use of keyboard requiring repetitive motion of fingers.nn nnExtensive use of telephone and face-to-face communication requiring accurate perception of speech.nn nnRegular sitting for extended periods of time.nn nnMay require occasional travel.nn nnAt IQVIA, we believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world.

The advanced analytics, technology solutions and contract research services we provide to the life sciences industry are made possible by our 67,000+ employees around the world who apply their insight, curiosity and intellectual courage every step of the way.

Learn more at .nn nn nIQVIA is an EEO Employer
– Minorities/Females/Protected Veterans/Disablednn nnIQVIA, Inc.

provides reasonable accommodations for applicants with disabilities.

Applicants who require reasonable accommodation to submit an application for employment or otherwise participate in the application process should contact IQVIA’s Talent Acquisition team at to arrange for such an accommodation.nn nn Posted 8 Days Ago nn nn Full time nn nn R1129634 nn n About Us n nn At IQVIA, we have a vision.

Where every healthcare decision is based on evidence.

Where data science and human science come together to improve global health.

Where new and creative solutions aren’t just possible – they are expected.

nn nn Thank you for your interest in growing your career with us.

It takes insight, curiosity, and intellectual courage to transform healthcare.

The 56,000+ employees of the IQVIA family of companies, including Q2 Solutions, are reimagining a world without the consequences of disease.

We are brave minds bringing powerful ideas to reality.

At IQVIA, you can truly make an impact in an environment where you’re supported to succeed.

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