Associate Study Start-up Manager

**Overview** To meet our client expectations and retain the excellent reputation built up over time the IQVIA PCS team is committed to recruiting, training and supporting driven individuals who have both consulting skills and life science skills that can be applied to PCS research activities. Individuals joining us are assured of a rewarding and progressive...

Additional Job Description The **Initiation Clinical Research Associate II **(**iCRA II**) 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 iCRA II can also support...

Additional Job Description The **Initiation Clinical Research Associate II **(**iCRA II**) 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 iCRA II can also support...

The Associate Project Manager ensures the successful initiation, planning, execution, monitoring, controlling and closure of assigned clinical research projects. The Associate Project Manager must ensure compliance with the study budget, project scope and timelines and in accordance with applicable standard operating procedures (SOPs), good clinical...

The **Initiation Clinical Research Associate II **(**iCRA II**) 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 iCRA II can also support protocol amendments if...

These customers have new therapeutic ideas, but want a partner who can assist with the clinical trial process, the complexities of certain disease states, or other critical capacities. You’ll work with them on the newest treatment breakthroughs for some of the most perplexing conditions. And ultimately, you’ll help make a positive difference in...

Role & Responsibilities - Development of Sponsor Project Plans (SPPs). - Establish project start-up timelines (including milestones, tasks lists, and dependencies) and track start - up progress through internal meetings and trackers. - Coordinate the development and communication of technical requirements to facilitate receipt of data transfers from...

Senior Clinical Trial Managers at Parexel FSP play a pivotal role in supporting, coordinating, and delivering our clients’ regional and global clinical trials. This includes full involvement in study start-up, maintenance, and close-out, as well as vendor management and CRA oversight. If you’re a Senior CTM with experience of these activities, we can...

ICON has an exciting new opportunity for a Global Project Manager to join a growing and successful team. This is a home-based and permanent role. Key Responsibilities: Responsible for: - Lead the development of realistic study timelines, from design through final study reporting Maintaining accuracy of clinical study timeline information in data control...

Parexel are currently recruiting for an experienced Oncology Associate Clinical Trial Manager. In this position you will be the individual responsible for the coordination of clinical operations required to initiate, execute and complete clinical trials to drive on-time delivery of clinical trial milestones. May act in support or lead role **Some specifics...

Founded in 1998 in Italy and now operating at an international level, OPIS is a full-service science driven biotech focused CRO providing premium trial management for multi-country clinical trials, including state-of-the-art information technology solutions and innovative approaches to the increasing complexity and variety of current projects. OPIS added...

Job Overview Associate Project Leads are an integral part of clinical trial delivery, liaising with clinical teams to improve patients’ lives by bringing new drugs to the market faster. The Associate Project Lead is a member of the core project team responsible for project delivery of clinical studies to meet contractual requirements in accordance with...

The Associate Director, Patient Recruitment defines recruitment & retention strategies and tactics, which are site and patient centric, as well as explores and implement innovative patient recruitment and site engagement strategies in close collaboration with both internal and external stakeholders and specialized patient recruitment vendors (when...

**The Project**: A new-age B2B SaaS company providing innovative solutions to reduce the frequency of cybercrimes and data breaches is in search of an experienced Product Marketing Manager to join their Founding team. The mission is to build a better internet where Good Data Brands can leverage their No-Code Policy Platform to build better, healthier...

**DESCRIPTION** The Manager, eTMF Operations oversees activities of the global eTMF Operations team (Regulatory Document Assistants, Senior Regulatory Document Assistants). The Manager, eTMF Operations also works with departmental functional leads and assumes a key role on supporting inspection readiness as a culture and compliance with GCP regulatory...

**Job summary**: As an experienced **Clinical Research Associate **you will be expected to actively participate in and manage the recruitment of potential investigators and perform CA and EC submissions. You will be responsible for monitoring of clinical sites, maintenance of study files, conduct of pre-study and initiation visits, liaison with vendors and...

ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development...

Within this role, you will be responsible for the planning, initiation, coordination and management of all monitoring and monitoring-related activities as well as supervision of all site-related activities to ensure compliance with SOPs, GCP and regulatory requirements. You will also engage with clinical sites to develop, build, and maintain strong...

You will be supporting a long-term partnership with one of the most established pharmaceutical companies in the industry. Within this program you will find a culture focused on teamwork and camaraderie; where every member plays an integral part. You will have the opportunity to work on breakthrough technologies in the areas of cardiovascular, oncology,...

Everything we do has the potential to impact patient lives, and our Clinical Research Associates (CRAs) take their work seriously, demonstrate empathy, and act with heart. They also perform with urgency, navigating our streamlined clinical operating model to drive effectiveness, reduce handoffs and increase employee, client and site satisfaction. As a CRA...