You have opted out of job matches in .
To undo this, go to the 'Skills and Interests' section of your preferences.
Shared by 
28 days ago
Requirements and responsibilities
EDETEK is seeking an experienced and highly motivated Senior Clinical Project Manager to lead the planning, execution, and oversight of clinical trials for pharmaceutical, biotechnology, and medical device clients. This role is responsible for cross-functional project leadership from study startup through closeout, with a strong focus on timeline management, sponsor communication, risk management, vendor oversight, and quality delivery.The ideal candidate will bring solid experience in a CRO environment and hands-on experience coordinating Data Monitoring Committee (DMC) activities, including meeting planning, deliverable readiness, communication management, and follow-up tracking. This individual must be able to manage multiple stakeholders, work effectively in a matrixed environment, and ensure studies are delivered on time, within scope, and in compliance with applicable regulations and company procedures.Essential Functions and ResponsibilitiesLead and manage clinical study activities from startup through closeout in accordance with protocol, sponsor requirements, project scope, budget, SOPs, GCP, and applicable regulations.Serve as the primary operational point of contact for assigned sponsors and maintain strong, professional sponsor relationships.Develop, maintain, and manage study timelines, project plans, status reports, action logs, and risk registers.Coordinate cross-functional teams, including clinical operations, data management, biostatistics, statistical programming, medical writing, safety, regulatory, and technology teams.Facilitate internal project meetings, sponsor meetings, and governance discussions, and ensure timely follow-up on action items.Monitor study progress and identify operational risks, quality concerns, and timeline issues, with proactive mitigation and escalation as needed.Oversee study vendors and external partners to ensure deliverables are completed with high quality and in accordance with project timelines and expectations.Support budget tracking, change order review, scope management, and resource planning in collaboration with leadership and other stakeholders.Ensure inspection readiness and support sponsor audits, internal audits, and regulatory inspections, as applicable.Promote effective communication and collaboration across global teams and functions.DMC Coordination ResponsibilitiesLead or support the coordination of Data Monitoring Committee activities for assigned studies.Develop and maintain DMC timelines, meeting schedules, communication plans, and tracking tools.Coordinate preparation of DMC deliverables, including data cuts, tables, listings, figures, reports, presentations, and meeting materials, in collaboration with biometrics and other relevant functions.Monitor readiness of DMC packages and ensure timely collection, review, quality control, and distribution of meeting materials.Organize DMC meetings, including logistics, document flow, agenda management, attendance coordination, and follow-up activities.Facilitate communication among sponsors, DMC members, independent statisticians, and internal study teams while maintaining required confidentiality and blinding controls.Ensure DMC activities are conducted in accordance with the DMC charter, study protocol, sponsor requirements, and applicable procedures.Maintain complete and accurate documentation of DMC decisions, recommendations, meeting minutes, and action items.RequirementsBachelor’s degree in life sciences, nursing, pharmacy, public health, or a related field required. Advanced degree preferred.Minimum of 7 years of clinical project management experience in the pharmaceutical, biotechnology, medical device, or CRO industry.Strong experience working in a CRO environment with sponsor-facing project responsibilities.Demonstrated experience coordinating or supporting DMC or IDMC activities in clinical trials.Strong understanding of ICH-GCP, clinical trial operations, and applicable regulatory requirements.Proven ability to manage multiple projects, priorities, and stakeholders in a fast-paced environment.Experience with study risk management, vendor oversight, and issue escalation.Strong organizational, analytical, and problem-solving skills.Excellent verbal and written communication skills.Proficiency in Microsoft Office and familiarity with clinical systems such as CTMS, EDC, eTMF, and related project tracking tools.Ability to work effectively with global teams across multiple time zones.Occasional travel may be required based on project or client needs.Preferred QualificationsExperience in oncology, rare disease, CNS, immunology, or other complex therapeutic areas.Experience managing global or multi-regional clinical trials.Familiarity with biometrics-related deliverables, including data review, interim analysis support, and reporting packages for DMC meetings.Experience working with decentralized trial tools, eClinical platforms, or integrated technology-enabled clinical solutions.Core CompetenciesClinical project leadershipSponsor relationship managementDMC coordinationCRO operationsVendor oversightRisk identification and mitigationCross-functional collaborationTimeline and budget managementQuality and compliance focusDecision-making and accountabilityBenefitsBenefits vary by country, but remain competitive. Below is a sample of the benefits offered to U.S. employees.Choice of comprehensive Medical, Vision and Dental Insurance plansPaid vacation time and sick daysCorporate holidays annuallyParticipation in the 401K PlanComprehensive perks and discount programs for AAA, wholesale, insurance, Rx, fitness, pets, entertainment, etc.Health Advocate and Employee Assistance ProgramLocation: This is a remote position, and we are open to candidates based in the United States, Argentina, and Brazil.
Optionally, you can add more information later (benefits, pre-screening questions, etc.)