Associate - Clinical Trials - Clinical Data - Indianapolis

+This is a remote position.+ · +The Clinical Data Manager (CDM) is responsible for the oversight, integrity, and quality of clinical trial data from collection through database lock.+ · ++Design and review Case Report Forms (CRFs) and Electronic Data Capture (EDC) systems to ensu ...

This is a remote position. · The Clinical Data Manager (CDM) is responsible for the oversight, · integrity and quality of clinical trial data from collection through database lock.This role collaborates closely with cross-functional teams to support timely and compliant study exe ...

This is a remote position. · The Clinical Data Manager (CDM) oversees clinical trial data collection through database lock · ensuring accuracy consistent with regulatory requirements. This role collaborates closely with cross-functional teams, · Clinical Operations Biostatistics ...

+Fully remote position at Labcorp. This is a Clinical Data Risk & Solutions Analyst (Global Monitor) role where you will be assigned a portfolio of clinical studies. · You will identify study risks and develop mitigation plans. · You will look for issues in the study data and sug ...

This role is responsible for trial level clinical data strategy including database structure content and meaning acquisition storage retrieval interchange delivery and representation. This requires an in depth understanding of data collection data flow management data quality dat ...

The Senior Data Quality · Analyst supports the accuracy, · completeness, and timeliness of immunization · information systems (IIS). ...

The Senior Data Quality Analyst supports the accuracy, completeness, and timeliness of immunization information systems (IIS). · ...

This position drives clinical research initiatives evaluating innovative programs' efficacy through analyses influencing clinical protocols enhancing members' health outcomes. · 5+ years of experience analyzing clinical or healthcare outcomes data. · Experience with cohort-based ...

We are looking for a Business Intelligence Lead with strong experience in Life Sciences Clinical Manufacturing systems and Good Manufacturing Practices (GMP). · Hands-on experience working with clinical manufacturing dataStrong understanding of GMP processesExperience with data f ...

The position involves files incoming cancer data reports from healthcare facilities electronically stores faxed mailed information conducts death clearance follow back updates cancer reporting healthcare facility contact information in software systems SEER*DMS Web Plus participa ...

The electronic Clinical Outcomes Assessment (eCOA) Build Programmer is responsible for designing programming testing clinical trial data collection databases including mapping testing normalization of data into a clinical data warehouse.This requires an in depth understanding of ...

CSI Companies is seeking an experienced BI Lead – Data Reporting & Analytics to support a Life Sciences organization operating within a clinical manufacturing and GMP-regulated environment. · Serve as the BI lead for reporting and analytics initiatives supporting clinical manufac ...

The eCOA Study Build Programmer is responsible for gathering and influencing eCOA design specifications to enable successful trial implementation. · Gather and influence eCOA design specifications to enable successful trial implementation · Program and test data collection system ...

We are seeking an eCOA Study Build Programmer to join our team. · Gatherand influence eCOA design specifications to enable successful trial implementation · Programand test data collection systems and associated data repository mappings for a trial or set of trials within a progr ...

eCOA study build programmer required for trial implementation · Gather and influence eCOA design specifications to enable successful trial implementation · Program and test data collection systems and associated data repository mappings for a trial or set of trials within a progr ...

We are looking for a BI Lead with mandatory Life Sciences Clinical Manufacturing Systems and GMP experience. · ...

We are seeking a highly experienced Senior BI Lead / Power BI Analytics Consultant with deep expertise in Life Sciences clinical manufacturing and GMP environments to support a Deloitte‑led modernization program by designing and delivering enterprise‑grade reporting solutions.The ...

This is a remote position for Biostatistician to design analyze and interpret clinical trial data to support drug development and regulatory submissions. · Collaborate with clinical and regulatory teams to design statistically sound clinical trials (e.g., sample size calculation ...

+Job summary · eCOA Build Programmer is responsible for designing programming and testing clinical outcome assessments for eCOA studies.+ · +Qualifications · <ul><li>Experience with eCOAProficiency in programmingClinical trial database managementStrong analytical skills</li></ul> ...

We are looking for a BI Lead / Data Reporting & Analytics Contractor with mandatory Life Sciences Clinical Manufacturing Systems and GMP experience. · Design, develop, and maintain reporting and analytics solutions to support business decision-making · Develop and maintain data m ...