Lead evaluation and redesign of business processes, drive change management initiatives (including ADKAR), and support implementation, documentation and training to ensure sustained adoption. Requires 5+ years' experience in change management, operations support or process improvement, with experience in CRO/pharmaceutical/biotechnology drug development and strong English communication skills.

Lead and support business and operational excellence activities including evaluating and redesigning processes, root-cause problem solving, developing recommendations, implementing change management (eg ADKAR), documenting processes, defining KPIs/dashboards, supporting training and stakeholder communications to ensure adoption and sustained improvements in clinical study operations. Minimum bachelor’s degree or equivalent and 5+ years relevant experience; experience in CRO/pharmaceutical/biotechnology drug development and knowledge of ICH-GCP noted.

The Senior Operations Specialist will lead process improvement and change management initiatives to improve delivery of studies for Sponsors. Responsibilities include business-process evaluation, root-cause analysis, designing and implementing process changes, stakeholder communication, training support, documenting processes, and establishing performance metrics. Requires 5+ years relevant experience and strong English communication; experience in CRO/pharmaceutical/biotech drug development and knowledge of ICH-GCP are specified.

The Senior Operations Specialist partners with cross-functional stakeholders to evaluate and redesign business processes, lead change management and training efforts, document processes, establish performance metrics and dashboards, and implement risk mitigation plans. Role requires 5+ years in change management/operations/process improvement and experience in CRO/pharmaceutical/biotechnology drug development; strong English communication and proficiency with Microsoft Office; knowledge of ICH-GCP.

The Senior Operations Specialist leads evaluation and redesign of business processes, drives change management (including ADKAR), develops training and documentation, and establishes KPIs and dashboards to monitor operational performance. Role requires 5+ years' experience in process improvement/change management within CRO, pharmaceutical, or biotech drug development and strong English communication skills.

Senior Operations Specialist to plan and manage initiatives that improve quality, efficiency and effectiveness of study delivery. Responsibilities include process evaluation and redesign, change management (including ADKAR), training and communication, documentation, KPI/dashboard monitoring, risk mitigation, and cross-functional stakeholder collaboration. Requires 5–7 years' relevant experience and strong English; experience in CRO/pharmaceutical/biotech and knowledge of ICH-GCP.

Serve as the primary operational point of contact for assigned FSP projects, coordinating cross-functional activities, monitoring risks/issues, supporting financial oversight, and preparing client-facing updates. Requires a bachelor's degree (or equivalent), a minimum of 3 years clinical research experience (3–5 years preferred) with at least 2 years leading a project, working knowledge of ICH-GCP and experience with clinical trial systems (EDC, eTMF, CTMS).

Responsible for providing program-level leadership and operational oversight for FSP projects, serving as primary client operational contact, coordinating cross-functional activities, monitoring risks and quality, supporting financial oversight, and contributing to onboarding and mentoring. Requires a bachelor's degree (or equivalent), strong knowledge of ICH-GCP and clinical operations, experience with clinical systems (EDC, eTMF, CTMS), and a minimum of 3 years clinical research experience with at least 2 years leading a project.

Provide program-level leadership and operational oversight for FSP projects, acting as primary client operational contact, coordinating cross-functional activities, monitoring risks/issues/quality, supporting financial oversight, and contributing to onboarding and mentoring. Requires a bachelor’s degree or equivalent, minimum 3 years clinical research experience (and minimum 2 years leading a project), strong English, knowledge of ICH-GCP, and experience with clinical trial systems (EDC, eTMF, CTMS).

Provide program-level leadership and operational oversight for assigned Functional Service Provider (FSP) projects, serving as primary operational contact for clients. Responsibilities include coordinating cross-functional activities, monitoring risks and quality trends, supporting financial oversight and forecasting, leading internal and client meetings, maintaining program processes/trackers, and contributing to onboarding and mentoring of FSP team members. Requires a bachelor’s degree (or equivalent), minimum 3–5 years clinical research experience with at least 2 years leading a project, strong knowledge of ICH-GCP and clinical trial systems, and proficiency with Microsoft Office.

Provide program-level leadership and operational oversight for assigned FSP projects, act as primary client operational contact, coordinate cross-functional deliverables, monitor risks/issues/quality, support financial oversight, and lead internal and client-facing meetings. Requires experience with clinical trial systems (EDC, eTMF, CTMS), strong knowledge of ICH-GCP and clinical operations, and proficiency in English.

Lead development of investigator/site budgets during proposals, manage global investigator grant workbooks, oversee payment processing and reconciliations, contribute to month-end close, and manage Sunshine Act and client reporting. Requires a bachelor's degree, at least 5 years clinical research experience and 3+ years in a leadership role.

Provide cross-functional project support for clinical studies including maintaining project timelines (MS Project), CTMS tasks (milestones, contacts, enrolment projections), meeting scheduling and minutes, TMF and study binder management, training coordination and records, SharePoint site setup, user access and helpdesk ticketing, study supplies and shipping coordination, and support for safety report distribution (IND/SUSAR) as needed. Requires a 4-year degree or equivalent, minimum 2 years relevant experience (e.g., Clinical Trial Assistant), professional-level English, proficiency in Microsoft Office, and working knowledge of ICH-GCP and regulatory guidance.

Precision for Medicine seeks an experienced Clinical Project Manager / Senior Clinical Project Manager to oversee full-service (Phase I–IV) oncology trials in a CRO environment. Responsibilities include project delivery across functional areas (data management, safety, clinical, medical monitoring, biostatistics), proposal and costing activities, client liaison, budget and timeline management, and cross-functional team leadership. Requires a life sciences degree (or equivalent), CRO full‑service project management experience (minimum 4 years), oncology trial experience, and working knowledge of GCP/ICH.

Lead and deliver global/regional phase I–IV oncology clinical trials in a full-service CRO setting, accountable for project scope, budget, timelines, quality and client relationship. Requires a life sciences degree (or equivalent), at least 4 years' full-service project management experience in clinical trials, CRO experience, knowledge of GCP/ICH, and proficiency with CTMS/eTMF/EDC/IXRS; travel availability required.

Lead and oversee full-service global/regional Phase I–IV oncology clinical trials within a CRO setting. Responsibilities include project delivery across functional areas (data management, safety, medical monitoring, biostatistics), proposal and budgeting activities, client liaison, and cross-functional team coordination. Requires a life sciences degree (or equivalent), at least 4 years full-service project management experience in clinical trials, Oncology experience, knowledge of GCP/ICH, and familiarity with CTMS, eTMF, EDC, IXRS and MS Project. Role requires domestic and international travel availability.

Lead and deliver full-service global/regional oncology clinical projects across all study stages (proposal, execution, closeout). Accountable for oversight of functional departments (data management, safety, clinical, medical monitoring, biostatistics), client relationship management, budgets and timelines. Requires a life-science degree or equivalent, at least 4 years full-service project management experience in a CRO, oncology experience, and working knowledge of GCP/ICH; willing to travel internationally.

Accountable for full-service oversight of global/regional Phase I–IV oncology trials including project delivery, cross-functional coordination (data management, safety, clinical, medical monitoring, biostatistics), proposal strategy and costing, client relationship management, budgets and timelines. Requires a life sciences degree or equivalent, at least 4 years' full-service project management experience in a CRO, knowledge of GCP/ICH, and experience with CTMS, eTMF, EDC and IXRS. Position is remote (Serbia) and requires domestic and international travel.

Precision for Medicine is hiring a Clinical Project Manager / Senior Clinical Project Manager to manage end-to-end (ph I-IV) Oncology trials in a CRO setting. Responsibilities include full-service project oversight, client liaison, proposal/costing activities, managing budgets and timelines, coordinating functional areas (data management, safety, clinical, medical monitoring, biostatistics), and preparing study documentation. Role requires at least 4 years' full-service project management experience in clinical trials and working knowledge of GCP/ICH.

Lead full‑service oversight of global/regional Phase I–IV oncology clinical trials for a CRO, accountable for project delivery, budgets, timelines, client relationships and cross‑functional coordination. Requires a life‑science degree (or equivalent), at least 4 years' full‑service project management experience in clinical trials within a CRO, knowledge of GCP/ICH, experience with CTMS/eTMF/EDC/IXRS, and availability for domestic and international travel.