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Assoc Mgr, Records Mgmt (R1041830) in Thane, India at IQVIA™

Date Posted: 12/5/2018

Job Snapshot

  • Employee Type:
  • Location:
    Thane, India
  • Experience:
    Not Specified
  • Date Posted:
  • Job ID:

Job Description

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.


Apply clinical research expertise to provide project related assistance across complex and multiple project(s), sites and project teams. Lead teams functionally, where assigned, including awareness of scope of work, budget, and resources. 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. Mentor/ coach Clinical Process Associate/Specialist colleagues.


 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/ trackers

 Ensure accurate completion and maintenance of internal systems, databases, tracking tools, timelines and project plans with project specific information

 Review, evaluate and recommend modifications to designated processes

 Oversee and participate in document management (creation, review, maintenance, storage, as applicable)

 Participate in (study) team meetings and implement action items

 Collaborate with the project lead/team members in creation/review of study documents including Quality manuals

 Act as point of contact for assigned deliverables for specific customers or projects

 Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations.

 Escalate quality issues to relevant stakeholders and/or line manager.

 Coach junior clinical process associate/specialists


 Advanced knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements;

i.e., ICH GCP and relevant local laws, regulations and guidelines, towards clinical trial conduct. Familiarity with related

systems and software’s utilized in clinical operations.

 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

 Ability to handle conflicting priorities

 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.

 Strong leadership skills

 Ability to work across cultures and geographies with a high awareness and understanding of cultural differences

 Act as a mentor for Clinical Process Associate colleagues

We 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™

Job ID: R1041830