Associate Director/Director Strategy, Real World Evidence and Late Phase - Morrisville, NC

The Principal Biostatistician is responsible for providing statistical support for pharmaceutical clinical trials in patients. · Collaborate with multi-disciplinary project teams to establish project objectives and timelines. · Write the statistical sections of clinical trial pro ...

Job Level: FSP Principal Biostatistician, Late Phase · Location: Home-based in the U.S. or Canada · Why DSSS? · Data Sciences Staffing Solutions, DSSS, is a unit within IQVIA that provides our sponsors with fully embedded resources through a Functional Service Provider (FSP) part ...

We are looking for an experienced Project Manager II to support our late-phase oncology research studies. As a key member of our team, you will partner closely with Medical Affairs and principal investigators to drive studies to completion and support their path to publication. · ...

We are looking for an experienced ISR/CO Study Manager to support our large portfolio of Investigator Sponsored Research (ISR) and collaborative (CO) studies. · Manage global ISR and collaborative studies ensuring compliance scientific integrity timely progression. · Serve as ope ...

Responsible for overseeing and coordinating all operational aspects of Real World Evidence (RWE) clinical studies and projects according to contract ensuring quality, timeliness, and client satisfaction from planning to completion. · ...

+Syneos Health is seeking a transformational executive leader to define scale commercialize the next generation of Real World Evidence RWE and Real World Late Phase RWLP solutions. · Responsibilities · Lead large-scale business transformation to modernize scale RWE/RWLP offerings ...

A leading fully integrated biopharmaceutical solutions organization is seeking an Associate Director of Real-World Evidence. The role involves managing RWE staff and overseeing real-world data analytics. · Provide line management and leadership to a cross-functional RWE team · Se ...

The Director of RWLP Operations leads cross-functional teams to deliver complex global research programs on time and within budget while fostering account growth and long-term client partnerships. · Leading cross-functional teams to deliver complex global RWLP programs on time an ...

The Associate Director Clinical Quality is responsible for providing strategic and operational GCP quality oversight across assigned clinical programs. · This role partners closely with clinical teams and stakeholders to ensure continuous inspection readiness, protect subject saf ...

The Clinical Monitoring Associate II role oversees clinical research studies by monitoring data and processes from a centralized location. · ...

Roles within Clinical Monitoring are responsible for overseeing and ensuring the integrity of clinical research studies by monitoring data and processes from a centralized location. · This includes conducting remote monitoring of trial sites to verify compliance with regulatory r ...

Clinical Research Associate II roles oversee clinical research studies by monitoring data and processes remotely. They ensure compliance with regulatory requirements and clinical protocols. · Perform site qualification, initiation, interim monitoring, site management activities. ...

Syneos Health is seeking a Clinical Research Associate CRA II to oversee and ensure the integrity of clinical research studies by monitoring data and processes from a centralized location. The successful candidate will conduct remote monitoring of trial sites to verify compliance ...

Clinical research associates oversee clinical trials to ensure data integrity. · Conduct site qualification and initiation visits · ...

Roles within Clinical Monitoring/CRA are responsible for overseeing and ensuring the integrity of clinical research studies by monitoring data and processes from a centralized location. This includes conducting remote monitoring of trial sites to verify compliance with regulatory ...

Syneos Health is looking for Clinical Research Associates (CRA) I/CRA II to oversee clinical research studies by monitoring data and processes from a centralized location. · ...

Sr. CRA II monitors clinical research studies to ensure compliance with Good Clinical Practices (GCP) guidelines. · ...

Updated: Yesterday · Location: Morrisville, NC, United States · Job ID: OTHLOC-1500-2DMI-2DR · Not ready to apply? · Join our Talent Network · Description · CRA II - FSP Sponsor Dedicated · Syneos Health is a leading fully integrated biopharmaceutical solutions organization built ...

Clinical Research Associates (CRAs) oversee clinical research studies by monitoring data and processes from a centralized location. · ...

Roles within Clinical Monitoring/CRA are responsible for overseeing and ensuring the integrity of clinical research studies by monitoring data and processes from a centralized location. · ...