We are looking for a Senior Regulator y Affairs Associate to join our growing team in Romania. This role can be either home or office based in Bucharest. As a Senior Regulatory Affairs Associate you will come with a few years of Regulatory Affairs experience gained in the industry. You will bring experience in Clinical Trail Applications (CTA) from various European locati

The Senior Initiation Clinical Research Associate ( Sr iCRA ) specialises in performing all study start up activities for a clinical trial. You will participate in Pre SIV activities and be assigned & accountable for managing and driving the strategy for the Pre SIV / start up tasks of the study. The Sr iCRA can also support protocol amendments if applicable. This role in

Manage Projects & Technology Lead and implement the setup of Data Receipt Agreements with vendors by working with cross functional teams. Programming and setup of Import procedures to allow the ingestion of data either using SAS or alternative technology (e.g. "Workbench") Programming of reconciliation checks to ensure appropriate transfer of data. Programming of offline

CRO GCP SOP SDV) IRB 4 / MR/CRC//// 202381

Due to a growing portfolio, we are currently looking for Project Quality and Risk Leads to be based in Serbia, Croatia or Turkey with flexible working hours. The Project Quality and Risk Lead assumes the lead (with support of LM or Mentor) of Quality oversight responsibility and partners with operational delivery teams focusing on first time quality, robust risk and issue

An exciting opportunity for Facilities Coordinator to join the Corporate Real Estate & Services (CRES) team. Do you have experience of working within a building services environment, excellent communication skills together with a professional customer service approach then we would like to hear from you! This position will be based at Parexel's Early Phase Unit in Berlin.

of the Role The Senior Statistical Programmer provides technical expertise for the conduct of clinical trials, acts as an internal subject matter expert in specific areas providing technical support and expert advice, and works independently to support various programing activities related to the analysis and reporting of clinical study data. In addition, the Senior Statis

1. Should have experience in eCTD, NeeS and paper formats. 2. Working experience in all major emerging countries (EU, GCC, US, ASEAN etc.) 3. Compilation, publishing, and technical quality control of Regulatory submissions including technical troubleshooting to ensure issues with submissions are resolved and deadlines met. 4.Should have experience in handling submission g

1. monthly closing for China statutory book 2. monthly quarterly tax filing related work 3. investigator drop file upload 4. account reconciliations 5. Statutory audit work

Are you currently a Physician Associate ? Are interested in pursuing a career in the Pharmaceutical Industry? We have an exciting opportunity for a Physician Associate the primary responsibility will be providing support to the Screening Department for human volunteer studies of new and existing pharmaceuticals performed in our Early Phase Clinical Unit (EPCU) in Harrow.

During the last five years, Parexel has participated in more than 1,000 Oncology and Hematology clinical projects. The range of services includes compound clinical development planning, collaboration with feasibility, protocol writing or optimization, medical monitoring and pharmacovigilance. Parexel has global presence in every phase of clinical research and expertise in

The Senior Director, Strategic Resource Lead is responsible for the oversight of a team of Managers and indirect reports of individual contributors. The Senior Director is an experienced leader capable of working independently, as well as providing strategic direction and guidance to the Resourcing managers and their teams, supporting on time delivery of high quality reso

Our Global Medical Services (GMS) organizational model/structure is aligned around key therapeutic franchises (5 franchises and 20 + Therapeutic Areas) to support high quality medical monitoring, leverage our expertise, strengthen, and build our customer relationships and drive new business. This position will report to the Senior Vice President, General Medicine. General

Support of high throughput, pre formulation, pre qualification, robustness, or admixture testing Results processing and documentation by following appropriate methods / protocols / procedures Sample management and monitoring of controlled temperature units Following all appropriate laboratory safety and hygiene procedures Qualifications BS (5+ yrs . ) o f relevant experie

Great opportunity to transition your clinical Pulmonary Medicine expertise to Parexel as an Associate Medical Director and make an impact globally! As an Associated Medical Director at Parexel, you will function as a medical representative on the project team, provide medical consultation as required or requested to clients and other Parexel service groups. Medical tasks