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Crinetics Pharmaceuticals · 3 weeks ago

Associate Clinical Project Manager

United States

Full-time

Onsite

Mid, Senior Level

$102K/yr - $127K/yr

5+ years exp

Crinetics Pharmaceuticals is a pharmaceutical company based in San Diego, California, focused on developing therapies for endocrine diseases. The Associate Clinical Project Manager will support the clinical project management team by managing the operational aspects of studies, collaborating with cross-functional teams, and contributing to the development and maintenance of processes related to clinical project management activities.

BiotechnologyHealth CarePharmaceuticalTherapeutics

Responsibilities

Provide routine and daily support to clinical project management team

Collaborate closely with clinical project management and cross-functional teams to establish priorities

Assist with development, maintenance, and management of high-quality detailed study timelines as assigned

Under oversight of CPM, may be assigned management of study(ies)

Support or management of routine status reporting, including study timeline and budget dashboards and management updates

Contribute to development of study budget and maintenance of monthly study budget forecasting and routine budget review in partnership with CTO and finance

Support cost accruals by study managers to ensure accurate reporting to finance and consistent approaches across all Crinetics-sponsored clinical trials

Collaborate with CPMs and study managers to collect and analyze forecasted and accrued costs to produce at-a-glance data displays summarizing project financial health

Collate and maintain current budget value by study based upon fully executed agreements

Routinely update and maintain an accurate listing of all current and planned studies

Support maintenance and timely updates to key tasks and milestones across studies to support Project and Portfolio Management for entry into corporate project management system

Share lessons learned and best practices across programs

Provide feedback and assist with the development of departmental procedures toward increased efficiency and quality of deliverables

Contribute to the development of procedural documents

Facilitate or oversee clinical project management team processes

Provide back-up support for CPMs as needed

Other duties as assigned

Qualification

Clinical project managementDrug development knowledgeBudget managementMS ExcelOrganizational skillsMatrix environment experienceCommunication skillsSelf-starterAttention to detail

Required

Bachelor's in related discipline required; a combination of relevant education and applicable job experience may be considered

5 years of related experience in a CRO, Biotech or Pharmaceutical organization is required

Solid understanding of drug development and clinical operations

Excellent organizational and time management skills and strong attention to detail, with proven ability to handle multiple tasks efficiently and effectively

Excellent computer skills including advanced knowledge in MS Excel, Word, PowerPoint and Outlook

Must be a self-starter who works with minimal supervision

Works effectively in a matrix cross-functional environment

Good business judgment and a strong understanding of the unique aspects of clinical financials

Excellent communication skills, (verbal and written) including the ability to understand and present budget information effectively

Works with high sense of accountability/urgency