Cedent Consulting Inc

This is a remote position.SummaryThe Clinical Operations Associate is responsible for ensuring efficient patientprovider assignments managing compliancerelated tasks and supporting enrollment processes. This dynamic role requires strong organizational and problemsolving skills to c More...

SummaryThe Director of Clinical Operations will leverage a strong scientific background and leadership expertise to advance programs from firstinhuman studies to laterstage development. This individual will integrate scientific clinical and business considerations into cohesive study More...

SummaryThe Clinical Outcomes Specialist provides expertise in the selection modification and development of neuropsychological endpoints across programs. This role involves contributing to clinical study design operational plans data quality monitoring and crossfunctional collaboratio More...

Position Summary:The Research Laboratory Manager will support the Principal Investigator in executing and maintaining research studies managing study documentation and supervising research study personnel. This role involves conducting experiments overseeing data collection and analys More...

Position Summary:As the Senior Director of Biostatistics you will lead and develop the statistical team within the assigned disease area ensuring statistical strategies align with clinical development objectives and regulatory standards. In this leadership role you will oversee the de More...

Position Summary:The Clinical Project Manager (CPM) will oversee and coordinate clinical activities across multiple projects while managing timelines communication and deliverables. This role involves working closely with crossfunctional teams investigational sites and stakeholders to More...

This is a remote position.Summary:The Clinical and Medical Affairs Administrator is a key role supporting the Clinical and Medical Affairs department focusing on contract execution budget oversight and operational support. This position ensures smooth coordination between Legal Fin More...

Summary:The role involves providing support for study coordination data management and regulatory activities within a Clinical Trials Office (CTO). This position ensures compliance with protocol guidelines internal procedures and regulatory requirements while assisting multidisciplina More...

Regulatory Affairs ConsultantLocation: Hybrid (Dallas TX Preferred)Yrs of Exp: 3 yrs Overview: We are seeking a highly skilled and detailoriented Regulatory Consultant to join our dynamic team in the medical device sector. This role will provide expert guidance on navigating complex More...

Summary:The Clinical Program Director is a fulltime role responsible for overseeing clinical operations program development and mental health initiatives. This position ensures highquality patient care and treatment outcomes through leadership and collaboration with medical staff.Resp More...

Summary:The Clinical Research Coordinator is a fulltime onsite role responsible for overseeing clinical research activities and ensuring the smooth execution of research studies. Key responsibilities include obtaining informed consent managing clinical trial protocols conducting resea More...

Summary:We are seeking a highly motivated and skilled individual to join our Antibody Discovery team as Scientist I. This open position is an exciting opportunity to impact the next wave of biologic candidates to enter our pipeline. The successful candidate should have general in vitr More...

Summary:The Clinical Trial Manager (CTM) is responsible for managing and supporting clinical trials in compliance with applicable regulations ICH/GCP guidelines and standard operating procedures (SOPs). The CTM works collaboratively with crossfunctional teams and partners with interna More...

SummaryThe Clinical Operations Director is responsible for overseeing the tactical implementation of the clinical development plan for autoimmune studies. This includes managing timelines budgets resources and clinical staff to ensure efficient and highquality execution of clinical tr More...

In this role you will work with the Clinical Data team to interpret and organize clinical oncology data. Reporting to the Clinical Data Manager you will develop realworld data variables from structured and unstructured sources design data capture forms and establish procedures for dat More...

Summary:The Clinical Research Coordinator II is responsible for managing and overseeing clinical trials working closely with a team under the direction of the Site Operations Manager. This role ensures smooth trial operations participant monitoring and data collection while maintainin More...

The Clinical Trial Associate supports the clinical operations project team to ensure the smooth execution of clinical trial processes in compliance with regulatory guidelines and ICH/GCP standards. This role involves managing trial documents coordinating project activities and assisti More...

Summary:This role provides global regulatory leadership and expertise to ensure compliance and successful submission of clinical regulatory filings. The position involves developing regulatory strategies managing submissions and maintaining communication with regulatory agencies and p More...

SummaryThe Director of Pharmacovigilance (MD) serves as a key medical and analytical leader responsible for the safety surveillance of investigational and/or marketed products. This role involves designing safety programs evaluating adverse event reports and collaborating with interna More...

Summary:The role involves developing and optimizing pipelines and algorithms for analyzing biological data particularly focusing on NextGeneration Sequencing (NGS) applications. This position requires collaboration with internal and external teams to refine algorithms conduct independ More...