Job Details

ID #51635536
Estado Pennsylvania
Ciudad Philadelphia
Full-time
Salario USD TBD TBD
Fuente Actalent
Showed 2024-05-06
Fecha 2024-05-07
Fecha tope 2024-07-06
Categoría Etcétera
Crear un currículum vítae
Aplica ya

Assistant Director Clinical Research Operations

Pennsylvania, Philadelphia, 19113 Philadelphia USA
Aplica ya

Description:The Clinical Trials Office (CTO) Assistant Director is responsible for assisting in all aspects of the CTO alongside the Sr. Director to collaborate and assist in the execution of CTO initiatives, manage day to day operations, assess staffing needs, complete administrative projects, and aid in MDG trial portfolio management and oversight. The incumbent will work closely with the members of the CTO as well as other Jefferson departments that impact clinical research. The candidate works alongside cancer center leadership to develop and execute CRO initiatives that align with the cancer center mission. Assists in the management of day-to-day operations of the Clinical Trials Office including interaction with Sr. Director of CTO, CTO project management and other departmental leaders; oversees selected MDGs and supervises respective project managers within the MDG Provides clinical trial education and awareness efforts to better efficiency and enhance clinical research quality, safety and performance as it relates to the protocols managed within the CRO as well as with other entities; Work closely with CRO staff and leadership to communicate MDG status, enrollment efforts and challenges. Manages initiatives to enhance the operations and logistics of the CRO; Participates in development, implementation and review of clinical trials; Identifies and collaborates with CRO and other hospital departments on clinical research process improvement initiativesSkills:Clinical trial, Clinical development, Oncology, Clinical research, Project management, Chart review, Regulatory, Data review, Clinical studyTop Skills Details:Clinical trial,Clinical development,Oncology,Clinical research,Project management,Chart reviewAdditional Skills & Qualifications: Bachelor’s Degree health-related field required; Master’s Degree preferred 8 years of experience in a Clinical Research setting; academic clinical research and/or oncology environment preferred Project management experience required working in clinical operations Knowledge of data management software and CTMS systems SOCRA or ACRP preferredExperience Level:Expert LevelAbout Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:

Hiring diverse talent

Maintaining an inclusive environment through persistent self-reflection

Building a culture of care, engagement, and recognition with clear outcomes

Ensuring growth opportunities for our people

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email [email protected] (%[email protected]) for other accommodation options.

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