Jonathan Roger Email & Phone Number

North Melbourne, Victoria, Au

Durham, North Carolina, Us

Coordinated functional team members and their activities across geographies, liaised with project management and the sponsor to ensure clinical deliverables (timeline, quality, and productivity) were met. Had overall accountability for the execution of the operational strategy and clinical plan including development of project tools, using basic analytical tools and assessing financial impact of decisions. In addition, responsible for implementing and instigating process improvement, responding to the needs of internal and external stakeholders, decision making with clearly communicated flow of action, actively encouraging open lines of communication, and prioritizing key issues.

München, Bayern, De

Created and managed the Canadian-based subsidiary. Responsible for investigating the legal aspects and differences with Europe. Full oversight on managing all financial aspects of the company.Oversaw all business development aspects. Development of innovative marketing strategy and tools, identifying, approaching and developing new leads. In charge of managing the clients’ database (CRM system)Supported all local and global operations activities. Supporting sponsors with their outsourcing process strategy and taking lead on the whole RFP process, from preliminary budget estimate to budget/contract execution. Involved in many Change Orders in-depth negotiations for reaching a fair compromise for all parties. Supported clients with budget controlling from study initiation to close-out as well as performing feasibility assessment via a data intelligence platform.

München, Bayern, De

Performed budget controlling for a phase 1/2a clinical trial. Project budgeting and forecasting preparation, monthly financial updates to assess compliance with the estimated budget, as well as driving change orders negotiations.

Yardley, Pa, Us

Coordinated clinical operations for a phase 2 Pediatric oncology study. In charge of overseeing all dedicated CRO’s activities with identifying gaps and failures, implementing corrective actions, supporting development and implementation of key study documentation as well as supervising the different vendors involved. Supported sites’ reengagement, developed and implemented strategies and tools for patients’ recruitment improvement.Responsible for overall clinical operations management for the department. Acted as single point of contact for all clinical operations-related activities, identifying opportunities for improvement, developing and implementing efficient cross-functional tools.

Montreal, Quebec, Ca

Managed a clinical research platform (COVID19 trials). Creating and managing a fully integrated new research unit. Identifying best-suited trials, negotiating budgets and contracts, overseeing all operational processes and staff. Assist PIs in the development of new investigator-driven studies (protocol, budget, grant submission). Development and implementation of effective patient recruitment strategies. Maintain an excellent relationship with sponsors, CROs and Principal Investigators. Ensure all relevant studies follow ICH-GCP guidelines.

Performed budget controlling for a phase 1/2a clinical trial. Project budgeting and forecasting preparation, monthly financial updates to assess compliance with the estimated budget, as well as driving change orders negotiations.

Supported contract management between sponsors and investigational sites. Contract officers’ management. Policies, procedures and tracking spreadsheets creation/improvement.

Montreal, Quebec, Ca

Managed a multidisciplinary research unit (HIV, HepC, NASH,…). Single point of contact for all stakeholders (Industry representatives, PIs, Nurses). Management of study start-up (study review and selection, budget and contract negotiation). Assist PIs in the development of new investigator-driven studies (protocol, budget, grant submission). In charge of multiple (>60) research accounts. Daily management of a research team (>10 staff members)

Montreal, Quebec, Ca

Coordinated a pan-Canadian investigator-initiated multicenter clinical trial (HIV). Including sites set-up, initiation and overseeing, management of investigators and study-coordinators networks, as well as real-time support, counselling and problems solving.Had responsibility for the entire department patient’s recruitment for many diverse sponsor-initiated trials (HIV, HepC, NASH,…). Over 120 patients recruited in more than 20 different phase 2/3 trials within 18 months.

Montpellier, Occitanie, Fr

Coordinated a national investigator-initiated multicenter clinical trial (vascular medicine). Including sites set-up, initiation and overseeing. Create and keep study documentation up-to-date and distribution. Interaction with all stakeholders

University Degree, Specialization In Clinical Research

Doctor Of Philosophy - Phd, Neurobiology And Neurosciences

Master Of Science - Ms, Physiology, Biomolecules And Therapeutics

Master Of Science - Ms, Cognitive Neuroscience