Sr. Clinical Process Associate, Clinical GDN

  • Company:
  • Location:
  • Salary:
    negotiable / month
  • Job type:
  • Posted:
    2 weeks ago
  • Category:
    Healthcare | Biotechnology/Pharmaceutical/Medicine

Skill: regulatory requirements , ich , gcp , life sciences , clinical , clinical research; Exp: 2-5 years; Sr. Clinical Process Associate, Clinical GDN – 1808714 Join us on our exciting journey! IQVIA is The Human Data Science Company, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics and human ingenuity to drive healthcare forward. Description PURPOSE Provide project related assistance for assigned complex project(s), sites and project teams. Ensure all work is conducted in accordance with SOPs, policies and practices, good clinical practices and applicable regulatory requirements and meets quality and timeline metrics. RESPONSIBILITIES Perform complex processes and tasks that eventually result in high quality deliverables that are completed according to service level agreements (SLAs) and within project timelines Establish and maintain effective project/ site communications Create and maintain relevant project documents Ensure accurate completion and maintenance of internal systems, databases, tracking tools, timelines and project plans with project specific information Participate in document management (creation, review, maintenance, storage, as applicable) REQUIRED KNOWLEDGE, SKILLS AND ABILITIES Good knowledge of applicable clinical research regulatory requirements; i.e., ICH GCP and relevant local laws, regulations and guidelines Strong written and verbal communication skills including good command of English language Results and detail-oriented approach to work delivery and output Good problem solving skills Good planning, time management and prioritization skills Attention to detail and accuracy in work Good software and computer skills, including MS Office applications including but not limited to Microsoft Word, Excel and PowerPoint Ability to establish and maintain effective working relationships with coworkers, managers and clients. Proven ability to work on multiple projects balancing competing priorities Ability to coach/ mentor junior colleagues Qualifications MINIMUM REQUIRED EDUCATION AND EXPERIENCE Bachelor’s degree in life sciences or related field and min 2 years relevant experience; or equivalent combination of education, training and experience PHYSICAL REQUIREMENTS Extensive use of keyboard requiring repetitive motion of fingers. Extensive use of telephone and face-to-face communication requiring accurate perception of speech. Regular sitting for extended periods of time. May require working in shifts. Connect to great opportunity Quintiles is a strong advocate of diversity and inclusion in the workplace. We believe that a work environment that embraces diversity will give us a competitive advantage in the global marketplace and enhance our success. We believe that an inclusive and respectful workplace culture fosters a sense of belonging among our employees builds a stronger team, and allows individual employees the opportunity to maximize their personal potential. Did You Know? Join UsWe know that meaningful results require not only the right approach but also the right people. Regardless of your role, we invite you to reimagine healthcare with us. You will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve human health outcomes. Whatever your career goals, we are here to ensure you get there! We invite you to join IQVIA. Primary Location IND-Kerala-Cochin Organization IND02 – India – CDS/Product Devel Job Clinical Research & Monitoring

Clinical Research


Experience: 2-5

Function: Biotech / Pharma / R&D