Source Job

• Lead global oncology clinical projects, managing full service oversight, budget, timelines, and cross-functional teams.
• Serve as primary client liaison, drive proposal strategy, and ensure high-quality trial execution from start to finish.
• Apply deep knowledge of GCP/ICH guidelines and use software like CTMS, EDC, and MS Project for efficient trial management.

Precision for Medicine enables precision medicine through novel clinical trial designs, advanced biomarkers, and data analytics, focusing on rare diseases and oncology. They are a people-focused CRO with a supportive, collaborative environment promoting work-life balance and team development.

• Monitor and own the progress of clinical studies at investigative sites, ensuring compliance with protocols, SOPs, ICH-GCP, and regulations.
• Coordinate all necessary activities to set up and monitor a study, including investigator identification, regulatory submissions, and pre-study/initiation visits.
• Identify potential study risks, propose solutions, and handle conflict using resolution strategies while maintaining quality and attention to detail.

Precision for Medicine, Oncology & Rare Disease is a precision medicine CRO that combines novel clinical trial designs, operational expertise, and biomarker analytics to advance oncology and rare disease treatments. The company fosters a culture with high CRA retention, small team influence, and a focus on work/life balance.

• Serve as primary point-of-contact and escalation point for clients, coordinating all functional services to meet timelines and budget.
• Manage the study budget, financial health, and project profitability, ensuring compliance and accurate forecasting.
• Develop robust project plans with risk management, maintain quality oversight, and lead internal and client meetings.

Precision for Medicine is a CRO that integrates clinical trial execution with deep scientific knowledge, laboratory expertise and advanced data sciences, focusing on Oncology and Rare Disease. The company has an operational scale and expertise to bring life-changing therapies to patients.

• Manage and deliver full clinical site monitoring services for complex multinational projects, ensuring compliance with SOPs, study guidelines, and GCP best practices.
• Act as Lead CRA, serving as primary liaison between CRAs and project teams, and participate in development of monitoring plans, protocols, and tools.
• Identify and recruit site investigators, oversee investigational site monitoring, and ensure site staff are compliant with training requirements.

Alimentiv is a clinical research organization providing monitoring and site management services for clinical trials. They are a full-time, permanent employer with a focus on building collaborative relationships and maintaining high standards in clinical study delivery.

• Monitor and own the progress of clinical studies at investigative sites.
• Ensure studies are conducted per protocol, SOPs, ICH-GCP, and all applicable regulations.
• Coordinate setup activities including investigator identification and regulatory submissions.

Precision for Medicine is a CRO integrating clinical trial execution with scientific and lab expertise, focusing on Oncology and Rare Disease. They have a strong culture with high CRA retention and emphasize work-life balance.

• Provide therapeutic and operational leadership throughout the clinical program and project delivery lifecycle.
• Collaborate with cross-functional teams to develop effective delivery strategies and resolve operational challenges.
• Ensure clinical projects within the assigned franchise are appropriately resourced and aligned with operational goals.

Our partner is a global clinical research organization dedicated to advancing healthcare innovation and improving patient outcomes through high-quality clinical trials. They offer a collaborative and inclusive environment with experienced professionals across global therapeutic and operational teams, focusing on professional growth and meaningful impact.

• Act as primary clinical point of contact with clients and lead planning, execution, and oversight of clinical studies across Latin America.
• Develop country-level recruitment strategies, guide monitoring and quality strategies, and mentor CRAs and partners.
• Collaborate with project managers on budgets, vendor management, and ensure compliance with ICH-GCP and regulatory requirements.

Precision Medicine Group is a precision medicine company that provides clinical research and commercialization services. The company is an Equal Opportunity Employer with a focus on expanding clinical operations across Latin America.

• Creates and maintains project timelines in MS Project or similar systems, ensuring accurate updates and distribution to team members.
• Coordinates internal and external meetings, prepares agendas, takes minutes, and files documentation in the Trial Master File.
• Manages study-specific training, system access, and supplies, while supporting team communications and vendor coordination.

Precision for Medicine is a Clinical Research Organization specializing in precision medicine, combining novel trial designs, operational expertise, and advanced biomarker analytics to advance oncology and rare disease treatments. The company fosters a collaborative, detail-oriented culture with a focus on professional growth and teamwork.

• Own and shape a regional start-up function, building scalable systems and playbooks for site activation across Central/Eastern Europe and Georgia.
• Drive site identification, feasibility, and readiness from CDA through activation, collaborating with sites, CROs, and sponsors.
• Monitor cycle times and use data to proactively identify bottlenecks and improve activation timelines.

Iterative Health is a healthcare technology and services company that accelerates clinical research to transform patient outcomes, specializing in gastrointestinal, hepatology, obesity, and cardiology. With 250+ employees worldwide, the company fosters a collaborative, low-ego culture focused on high ownership and accountability.

• You will monitor and own the progress of clinical studies at investigative sites, ensuring compliance with protocols, SOPs, ICH-GCP, and regulations.
• You will coordinate all activities to set up and monitor a study, including identifying investigators and preparing regulatory submissions.
• You will travel domestically up to 50-60% for site visits and maintain fluency in English and local language.

Precision for Medicine is a clinical research organization focused on precision medicine for oncology and rare diseases. They are a smaller CRO with a strong culture and high employee retention.

• Provide study oversight as primary liaison between CRAs, internal staff, site staff, client personnel, and external vendors.
• Ensure clinical monitoring activities comply with SOPs, regulations, GCP, KPIs, and study-specific requirements.
• Develop and manage clinical plans and guidelines, including the clinical monitoring plan and study timelines.

ProTrials is a women-owned, WBENC-certified Contract Research Organization (CRO) that has been a trusted partner in clinical research since 1996, supporting research behind innovative treatments in pharmaceutical, biotech, and medical device industries. They foster a collaborative community where team members feel valued, supported, and empowered to make a meaningful impact on global health.

• Lead site activation strategies and oversee start-up activities across clinical studies.
• Manage critical path plans and mitigate risks to ensure timelines are met.
• Collaborate with cross-functional teams and clients to improve activation processes.

Our partner is a clinical research organization that supports the delivery of clinical trials. They are a global company with a collaborative culture focused on innovation and operational excellence.

• Serve as primary point-of-contact and escalation point for clients, coordinating all functional services and external vendors.
• Manage study budgets, project profitability, and billing compliance to ensure financial health and alignment with scope.
• Develop robust project plans, track metrics, and prepare status updates for clients and senior management.

Precision Medicine Group is a global contract research organization specializing in oncology and precision medicine. The company values collaboration and quality, employing a diverse team of professionals dedicated to advancing clinical research.

• Act as a strategic partner for key customers, leading governance, growth initiatives, financial performance, and cross-functional collaboration.
• Lead and oversee global, multiregional, or complex regional Clinical FSP partnerships, ensuring alignment with contractual agreements and strategic priorities.
• Provide executive oversight for clinical FSP delivery, ensuring quality, timelines, key performance indicators, and contractual commitments are achieved.

The employer is a global clinical research organization that partners with pharmaceutical and biotech companies to deliver clinical trials. They are a large, established company with a culture focused on innovation, collaboration, and advancing healthcare worldwide.

• Manage line management of CRAs, IHCRAs, and CTMs across European regions, ensuring performance and development.
• Drive operational excellence initiatives and resource deployment to optimize clinical trial execution.
• Partner with leadership to identify quality risks, implement corrective actions, and support workforce planning.

Precision for Medicine is a precision medicine-focused clinical research organization that uses biomarkers and data to advance oncology treatments. The company fosters a culture of collaboration, continuous learning, and high performance.

• Manage project scope, timeline, and delivery of quality products and services for clinical trials.
• Align expectations and communicate effectively with stakeholders across internal teams and clients.
• Track project financials, manage risks, and support continuous improvement initiatives.

eClinical Solutions provides expert data services and a clinical data cloud platform to accelerate clinical development for life sciences organizations. They are a fast-growing, people-first organization with a remote culture and have won Top Workplaces awards.

• Serves as clinical trial lead, overseeing study planning, conduct, and oversight per protocol and regulations.
• Develops study documents, manages site feasibility, and drives recruitment strategies.
• Leads internal clinical team meetings and ensures quality deliverables through metric reporting.

Precision Medicine Group is a life sciences company that supports clinical research and development. The company is large enough to offer a range of benefits and emphasizes a collaborative, ethical culture focused on quality and compliance.

• Serve as the primary point of contact and partner with investigative sites to ensure high-quality clinical trial conduct.
• Conduct site evaluation, training, monitoring, and closure activities in compliance with regulations, GCPs, and SOPs.
• Utilize risk-based monitoring and site engagement strategies to improve data integrity, compliance, and study performance.

AbbVie discovers and delivers innovative medicines and solutions across immunology, oncology, neuroscience, and aesthetics. A large global biopharmaceutical company, AbbVie fosters a culture of innovation and integrity to transform patients' lives.

• Lead the study start-up process, developing strategy and coordinating regulatory deliverables to meet targets.
• Serve as primary contact for start-up activities, prepare and review regulatory documents, and ensure compliance with ICH-GCP and regulations.
• Manage essential document collection, site correspondence, contract negotiations, and support team training and budget monitoring.

Ergomed is a mid-sized contract research organization specializing in oncology and rare disease. The company has a global presence with operations in Europe, North America, and Asia, and emphasizes employee well-being, work-life balance, and career development.

• Develop, mentor, coach and manage CTMs to progress their skillset per quality standards.
• Collaborate with management to enhance CTM expectations and procedures for quality and efficiency.
• Ensure CTMs have proper resources and training to deliver high-quality study conduct.

Precision for Medicine is a clinical research organization (CRO) that provides clinical trial management services. The company employs a large team of clinical research professionals and emphasizes quality and collaboration.