Clinical Data Specialist

We are seeking a skilled Clinical Content Specialist to join our team.Key Responsibilities:    Develop high-quality key clinical trial documents, including protocols, Investigator's Brochures (IBs), Informed Consent Forms (ICFs), Case Report Forms (CRFs), and Clinical Study Reports (CSRs).    Translate complex scientific data into clear, regulatory...

Job Title: Clinical Support SpecialistDescription:We are seeking a detail-oriented and organized individual to join our team as a Clinical Support Specialist. In this role, you will be responsible for handling high-volume clinician/clinic communications, maintaining accurate records, and performing end-of-day QA tasks.This is a repetitive, SOP-driven...

Medical Oncology SpecialistWe are seeking a skilled Medical Oncology Specialist to join our team.Key Responsibilities:Clinical Expertise: Diagnose and treat cancer patients using various medical oncology techniquesTreatment Planning: Develop and implement treatment plans to ensure optimal patient outcomesTeam Collaboration: Collaborate with multidisciplinary...

Job Title: Data Curation SpecialistOverview:As a Data Curation Specialist, you will play a pivotal role in ensuring the quality and consistency of biological datasets.Responsibilities:Identify, curate, and annotate biological datasets from various sources using APIs and AI tools.Automate curation of large interaction datasets to decrease curator...

Lead Clinical BiostatisticianWe are seeking an experienced Lead Clinical Biostatistician to play a critical role in developing, implementing, and overseeing statistical strategies for sponsored clinical trials. This position involves leading biostatistics teams, contributing to study design discussions, authoring statistical analysis plans, and providing...

Job Opportunity:We are seeking a skilled professional to fill the role of Senior Statistical Programmer. In this position, you will be dedicated to working with clinical trial data in the pharmaceutical industry.Key Responsibilities:Manipulate and analyze large datasets using SAS programming.Generate and validate SDTM and ADaM datasets, as well as tables,...

Job Overview:We are seeking a skilled professional to provide day-to-day clinical quality assurance support across ongoing clinical trials.The ideal candidate brings strong experience with Veeva QMS, is highly tech-savvy, and can support clinical operations teams in a fast-paced, remote environment.

About Us:We are a global IT services company headquartered in the United States. Founded in 1996, we specialize in digital engineering and IT services helping clients modernize their technology infrastructure, adopt cloud and AI solutions, and accelerate innovation.Our company operates in over 50 locations across more than 25 countries, has delivery centers...

Clinical Systems Tester Job">Job Summary:">We are seeking a skilled Clinical Systems Tester to support testing and validation activities within a Decentralized Clinical Trial environment.">Responsibilities:">Author and execute test scripts in Veeva EDC, aligned with protocol requirements.Validate workflows across eCOA and IRT platforms.Participate in system...

Medical Scribe Role: Administrative Assistant\This role involves handling templated clinician/clinic communications, records hygiene, and daily logs. The work is repetitive and SOP-driven, with no calls or sales involved. Confidentiality is a top priority.\The ideal candidate will have strong written UK English skills and be comfortable with monotony. They...