Apply on Employer Site

Emmes · 1 week ago

Director, Project Delivery - Global Project Management, Ophthalmology

United States

Contract

Remote

Director/Executive

7+ years exp

Emmes Group is transforming the future of clinical research, bringing the promise of new medical discovery closer within reach for patients. The Director, Project Delivery is responsible for overseeing clinical project management globally, ensuring effective leadership and client satisfaction throughout the project lifecycle.

BiopharmaBiotechnologyClinical TrialsHealth CareMedical

Responsibilities

Responsible for project delivery oversight of assigned Emmes Book of Business globally

Collaborates Therapeutic Leads and subject matter experts to develop Best Practices, Monthly project reviews, Templates library, Bid Defaults

Consults in the development of RFPs for biopharma clients, identifying appropriate strategy, team structure, preparing proposal language, and developing budget and timelines in collaboration with leaders and key subject matter experts (SMEs)

Provide ongoing mentorship, coaching, feedback, and ongoing training to Project Managers including addressing performance issues, conducting formal performance appraisals, and creating development plans

Ensures appropriate training occurs and evaluates proficiency or additional training needs of PM staff

Provides oversight of operational deliverables and financial health of projects

Serves as a point of escalation for PMs, sponsors, and other functions relative to overall project management in a study governance capacity

Develops successful working relationships with clients, executive management, and functional leads to provide oversight of project issues, proactively identify and mitigate risks and drive milestone achievement

Ensures PMs are tracking project deliverables against contract using Emmes’ tools & Key Performance Indicators, as defined by the project or organizational metrics

Reviews study metrics to ensure risk mitigation and performance according to contract. Monitor trends and drive changes to project management as needed

Ensures adherence to quality control expectations and milestone timelines for delivery of contractually required reports and deliverables

Ensures changes in scope are identified and managed appropriately. Support PMs in collaborations with Business Development, Contracts Department, and executive management to ensure timely execution of contract amendments/change orders

Presents and prepares PMs to present in bid defense meetings in collaboration with Business Development Lead or other key stakeholders

Identifies and documents lessons learned from study successes and challenges to promote development of best practices and work with global colleagues to develop or revise standards for best practice

Support the identification and implementation of tools and process integrations that support the efficiency and productivity of PMs. This may include, but is not limited to collaboration with internal stakeholders and vendors to support global, PM efficiency and standardization within the department

Models and propagates Emmes’ commitment to a culture of quality in all aspects of our deliverables, utilizing a solution-based, science-driven, value-added approach in collaborating with clients

Other duties as assigned

Qualification

Clinical Project ManagementClient Relationship ManagementRegulatory Compliance (ICH/GCP)Clinical Trial Management SystemsProject LeadershipCoachingFinancial OversightRisk MitigationMS Office SuiteMentorshipTeam Management

Required

Bachelor's degree in a scientific discipline

Minimum 7 years demonstrating scientific principles appropriate in managing a clinical research portfolio inclusive of 3 or more years in a pharmaceutical and/or CRO setting, serving in a global Clinical Trial Team Lead or Project Management role or equivalent position

Demonstrable track-record of success delivering complex/high priority clinical trials within agreed time, quality and cost working across multiple therapeutic areas, phases 1-3, in a global capacity

Demonstrated experience in developing and fostering strong client and internal relationships

Thorough understanding of International Conference on Harmonization (ICH) Good Clinical Practice (GCP) and knowledge of SOP's guidelines and regulatory requirements

Skilled in MS Office Suite of products and working knowledge of Clinical Trial Management Systems, electronic Trial Master File, and electronic Data Capture systems and solutions and project support tools

Demonstrated experience in managing diverse staff and leading successful teams with direct and indirect supervision responsibilities

Travel between corporate locations and client sites as appropriate