IQVIA is changing an entire industry through inspired innovation. Our People make the difference. We believe that great ideas can come from anywhere. Great products come from great ideas. And great ideas come from great people. We look for the very best people and then give them meaningful work to do. Join IQVIA and help us make the world a better place.
Direct and manage the day-to-day activities of the clinical research office ensuring studies are appropriately planned and resourced and staff are trained and developed to meet the needs of all trials. Assist with the clinical research financials and help track, report on, and proactively manage performance metrics.
Assist with the management of training, planning and preparation of new studies including:
Supervise and coordinate team activities to ensure that team goals are met and to ensure studies are carried out according to protocol, standard operating procedures (SOPs) and applicable guidelines and regulations and within budget;
Help plan logistical activity for procedures as per protocol and ensure thorough resource planning;
Identify risks on study and ensure that actions are implemented to mitigate these;
Ensure study specific training materials, documents, and records are prepared and deliver or coordinate training, dry runs, simulations and tests as required;
Oversee the administration and custody of investigational product and comparator medicines according to Avacare standard operating procedures;
Manage staff in accordance with organization’s policies and applicable regulations. Responsibilities include:
Plan, assign, and direct work;
Appraise performance and guide professional development;
Address employee relations issues and resolve problems;
Provide training to new staff members on study-specific topics and new clinical skills;
Ensure compliance with staff training requirements by auditing and maintaining training records;
Drive quality and process improvement efforts to support control of site budget, development of the facilities and services and the culture towards a high-performing and efficient team;
Drive the collection of metrics and dissemination of the results and develop and implement plans to address issues and areas of concern;
Cover weekend, evening and night on-call responsibilities as required;
Update and maintain skills, training and knowledge of topics related to clinical research.
In-depth knowledge clinical trials
In-depth knowledge of the principles of Good Clinical Practices (GCP) as per IQVIA mandated training
In-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedules
Effective skills in using MS Windows and Office applications such as Outlook, Excel, and Word
Effective written and verbal communication skills including good command of the English language
Excellent interpersonal skills
Excellent problem-solving skills
Effective organizational skills
Ability to pay close attention to detail
Ability to establish and maintain effective working relationships with coworkers, managers and clients
Applicable certifications and licenses as required by company, country, state, and/or other regulatory bodies
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