Clinical Trial Manager - Germantown

Description · The Clinical Trial Manager (Germantown Hybrid) serves as the primary client contact and leads all aspects of clinical study execution—from kickoff through CSR completion and regulatory submission. This role ensures seamless project delivery by driving timelines, man ...

The Clinical Trial Manager serves as the primary client contact and leads all aspects of clinical study execution. · ...

Clinical Trial Manager II is responsible for the execution of operational activities for a study or group of studies at a regional level or within a small group of countries. · Possesses detailed knowledge of the study/protocol and its associated activities and timelines, · ...

Clinical Trial Manager II is responsible for the execution of operational activities for a study or group of studies at a regional level or within a small group of countries. · ...

We are growing our team to help revolutionize precision heartcare. · The Clinical Trial Manager (CTM) oversees and manages all clinical operational activities at the trial and site level. · Responsibilities include developing clinical trial timelines, managing study documentation ...

Clinical trial manager with experience in clinical research operations and regulatory compliance. Responsible for the execution of operational activities for studies or groups of studies at a regional level or within a small group of countries. · ...

Redefining What Accessible Means in Cancer Care · United Theranostics is redefining the clinical practice of molecular imaging and radiopharmaceutical therapy — from available to meaningfully accessible. Our network of nuclear medicine facilities specializes in personalized cance ...

Job Requisition ID # · 26WD95541Position Overview · We are seeking an eCommerce Innovation – Trial Modernization Manager to help accelerate trial monetization and modernize trial experiences for our next-generation offerings. This mid-level individual contributor role focuses on ...

The Study Operations Manager I has responsibilities for study activities from startup through conduct and close on one or more studies. · Serves as leader of the local study team on one or more studies · Liaises with colleagues in country to agree on submission strategy to Health ...

Senior Clinical Data / Protocol Manager · Location: Federal Agency – Intramural Clinical Research Program · Contract Term: 1–4 Years · Are you an experienced clinical research professional with deep expertise in human subject research and IND trials? A Federal Agency is seeking a ...

Job Requisition ID # · 26WD95541 · Position Overview · We are seeking an eCommerce Innovation – Trial Modernization Manager to help accelerate trial monetization and modernize trial experiences for our next-generation offerings. This mid-level individual contributor role focuses ...

Senior Clinical Data / Protocol Manager · Location: · Federal Agency – Intramural Clinical Research Program · Contract Term: · 1–4 Years · Are you an experienced clinical research professional with deep expertise in human subject research and IND trials? A Federal Agency is seeki ...

This is the upper tier of the middle management BioPharma Services Quality Assurance career track. · Provides general or direct supervision including but not limited to: interviewing, hiring, and training employees - planning, assigning, and directing work - administering perform ...

Precigen is seeking a highly motivated and skilled Head of Clinical Operations (level determined by candidate experience), to drive our clinical trial programs to develop next generation gene and cell therapies focused in immuno-oncology, autoimmune disorders, and infectious dise ...

Precigen is seeking a highly motivated and skilled Head of Clinical Operations to drive our clinical trial programs. · ...

Description · Design, develop, and manage Electronic Data Capture (EDC) systems and electronic Case Report Forms (eCRFs) for clinical studies. Develop and implement data validation checks to ensure data integrity, accuracy, and completeness. Identify, investigate, and resolve dat ...

+Job summary · This Jobbot Job is hosted by Audrey Block. · +ResponsibilitiesDevelops strong investigative site relationships and ensures continuity of investigative site relationships through all phases of the trial. · Conducts site visits including but not limited to Pre-study ...

This role will be responsible for hands-on GMP manufacturing operations, production planning, documentation generation and equipment and materials oversight ensuring day-to-day readiness for clinical manufacturing of our oncology cell therapy product. · ...

This role will be responsible for hands-on GMP manufacturing operations, production planning, documentation generation and equipment and materials oversight ensuring day-to-day readiness for clinical manufacturing of our oncology cell therapy product. · ...

Position: Lab Instrument Service Specialist · Salary Range: $80K-$100K · Location: Germantown, MD · Unfortunately, we cannot support work visa permit applications for this role · About Pharmaron · Pharmaron is a global CRO (Contract Research Organization) helping pharma and biote ...