Excellence in Clinical Trials based remotely reporting to the Director, GCP Excellence in Clinical Trials. At Takeda.../ECs and with QA to ensure adherence to the plan. Oversee global and program aligned GCP Excellence in Clinical Trials...
in Clinical Trials based remotely reporting to the Associate Director, GCP Excellence in Clinical Trials. At Takeda... execution teams in alignment with GCP Excellence in Clinical Trials leadership. ACCOUNTABILITIES: Provide support...
. If this is your profile, we want to hear from you. Job Summary The Associate Director, GCP Quality Assurance oversees GCP activities..., and support operational excellence Independently conduct Clinical Investigator Site Audits, GCP Document Audits (Clinical Study...
Job Description Job Overview: We are seeking a highly qualified and experienced Associate Director in Data Management... to lead our data management team in supporting the pharm and vaccine veterinary clinical trials. The ideal candidate...
. If this is your profile, we want to hear from you. Job Summary The Associate Director, GCP Quality Assurance works within the Global... excellence · Independently conduct Clinical Investigator Site Audits, Vendor Audits, GCP Document Audits (Clinical Study...
. Here, you will be a vital contributor to our inspiring, bold mission POSITION OBJECTIVES: The Associate Medical Director leads... and development feasibility, evaluating complete or ongoing clinical trials, and regulatory interactions and future development plans...
of clinical trials (Phase I-III). The Associate Director will be a leader in the organization who knows how to manage a team...Job Title: Associate Director, Clinical Operations Job Location: San Carlos, CA, USA Job Location Type: Remote...
. Job Description Associate Director, Clinical Pharmacology - Virology *This is a site-based position in Foster City, CA or Parsippany, New... in clinical trials and develops solutions for these using precedents and original thinking. Adheres to regulatory requirements...
SUMMARY/JOB PURPOSE: The Clinical Operations Associate Director combines end-to-end design, execution, and reporting...) and delivering these to target or stretch thresholds. The Clinical Operations Associate Director is the Study Delivery Lead (SDL...
: An Associate Director, Data Management is operationally responsible for the oversight of Clinical Data Management activities... Associate Director DM will provide oversight to ensure end-to-end data management consistency across the portfolio. The employee...
excellence. Thorough knowledge of FDA and EMA regulations, ICH guidelines, and GCP governing the conduct of clinical studies... agencies. Anticipates problems that may arise in clinical trials and develops solutions for these using precedents...
Job Description: Overview The Associate Director, Biostatistics is responsible for statistical activities... in support of clinical trials, including contributing to trial designs, authoring statistical sections of protocols...
The Associate Director acts as a statistical expert supporting the clinical development of compounds as compound... as described below. The Associate Director contributes to clinical development strategies and plans. Responsibilities: Compound...
strong leadership, GCP expertise and clinical operations experience to drive the monitoring strategy for trials in their assigned...Job Description: Responsibilities: The Associate Director, Site and Monitoring Health will provide...
Job Description: The Associate Director, Biostatistics is responsible for statistical activities in support... of clinical trials, including contributing to trial designs, authoring statistical sections of protocols, preparing statistical...
and data to clinical trials to facilitate decision-making across the portfolio. The candidate will support an innovative... group as a biomarker development expert to support genomics-based biomarker assays/technologies to support the clinical...
clinical trials under regulated settings (GLP, GCP, GCLP and CAP/CLIA etc.). Experience within GI, immunology, neurology..., and implementation strategies to deliver key assays and data to clinical trials to facilitate decision-making across the portfolio. The...
’s global safety database. Responsible for development and maintenance of Safety Management Plans for Alnylam clinical trials... processes and procedures for clinical trial ICSR processing activities, including oversight of the case processing outsourced...
-initiated and industry-sponsored human subject clinical trials. The individual will work under general supervision of the... Clinical Program Operations Director and will be required to perform responsibilities with a limited degree of independence...
and apply regulations in practice. The CRC II will assure that the integrity and quality of clinical research trials is maintained and the... and financial functions of the Center of Excellence for Clinical and Translational Research. Daily Operations Assess eligibility...