Associate/Clinical Project Manager (Client Dedicated)

Job Overview

Associate Clinical Project Managers 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 Clinical Project Manager is a member of the core project team responsible for project delivery of clinical studies to meet contractual requirements in accordance with SOPs, policies and Company practices. Clinical Project Management is focused on project delivery, productivity and quality resulting in strong financial performance and customer satisfaction. The Associate Clinical Project Manager has distinct responsibilities supporting the efforts of the Clinical Project Manager to drive operational excellence and strategic leadership with our customers. Associate Clinical Project Managers may run their own studies as part of their development and/or manage the Project's Third-Party Vendors.

Essential Functions
• Provide input in to the development of integrated study management plans with the core project team and/or sub-team, within a client-dedicated team.
• Accountable for assigned portion of clinical studies as per the contract while optimizing speed, quality and cost of delivery and ensuring consistent use of study tools and training materials and compliance with standard processes, policies and procedures.
• Set objectives of project sub-team(s), according to agreed upon contract, strategy and approach, effectively communicate and assess performance.
• Collaborate with other functional groups within the company where necessary to support milestone achievement and to manage study issues and obstacles.
• Monitor progress against contract and prepare/present project and/or sub-team information proactively to internal stakeholders. Support the project leader to prepare/present project and/or sub-team information proactively to external stakeholders.
• Identify risk (positive and negative) and contingencies and partner with project leader in problem solving and resolution efforts.
• Achieve project quality by identifying quality risks and issues, responding to issues raised by project sub-team members and partner with project leader planning/implementing appropriate corrective and preventative action plans.
• May serve as primary (for small projects) or back-up project contact with customer.
• Lead the efforts of a project sub-team, responsible for managing cross-collaboration of the sub-team to support milestone achievement and to manage issues and obstacles.
• Support the project leader in ensuring the financial success of the project.
• Forecast and identify opportunities to accelerate activities to bring revenue forward in partnership with the senior project leader.
• Identify changes in scope and partner with project leader to manage change control process as necessary.
• Identify lessons learned and implement best practices.
• May be assigned as the primary contact for vendors leading project vendor management and vendor management related activities as per project requirements

Qualifications
• Bachelor's Degree In life sciences or related field required
• More than 1 year of Clinical lead, Clinical Trials Manager, Project Management experience preferred.
• Knowledge of clinical trials - 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. Broad protocol knowledge, therapeutic knowledge desired.
• Communication - Strong written and verbal communication skills including good command of English language. Strong presentation skills.
• Problem solving - Strong problem solving skills.
• Organisation - Planning, time management and prioritization skills. Ability to organize resources needed to accomplish tasks, set objectives and provide clear direction to others, experience planning activities in advance and taking account of possible changing circumstances.
• Prioritisation - Ability to handle conflicting priorities.
• Quality - Attention to detail and accuracy in work. Results-oriented approach to work towards delivery and output.
• IT Skills - Good software and computer skills, including MS Office applications including but not limited to Microsoft Word, Excel and PowerPoint.
• Finances - Good understanding of project financials.
• IQVIA Core Competencies - Ability to demonstrate all IQVIA competencies (Client Focus, Collaboration, Communication, innovation, Ownership).
• Available for Home-based

근무형태/장소

- 업무 형태 : 재택근무가 가능합니다.

- 근무 장소 : IQVIA 잠실 오피스 (송파구 송파대로 558 월드타워빌딩 13층, 2/8호선 잠실역 도보 4분)

채용 전형

- 이력서 접수 > 서류전형/Pre-screening > 면접전형 > 최종합격 > 입사

- 지원 방법 : 영문 CV를 첨부하여 본 공고를 통해 지원 (이력서 양식 자율)

- Pre-screening 전형 :

- 면접은 화상 혹은 대면으로 진행되며, 지원자 가능 일시에 맞추어 조율됩니다.

- 각 전형 결과는 합격/불합격 여부와 관계없이 모든 지원자에게 안내됩니다.

- 국가등록장애인 및 국가보훈 대상자는 관련법에 의거하여 우대됩니다.

- 지원서 내용이 사실과 다른 경우 합격이 취소될 수 있습니다.

Life at IQVIA

- 조직 내 다양한 Internal Career Development 의 기회

- Employee Assistance Program (직원 고민 상담 지원 프로그램, 가족 포함)

- 사내 동호회, 팀워크샵, 팀빌딩, 연말파티 등 다양한 Activity 지원

- 다양한 경조 패키지 (경조금/경조휴가/상조용품), 호텔 프로모션/리조트 멤버십 지원

- 명절상여금, 영유아 위탁교육비, 업무용 휴대폰(iphone) 지급

- 재택근무 활성화 및 모바일 오피스, Flexible working hours 운영

- 단체보험 (생명/상해보험, 배우자/자녀 포함) 및 건강검진 패키지 지원

- 연차 외 특별휴가 (Company day, 유급병가) 등

- 직원 추천 보너스 제도

추천 영상
1. What does it mean to be IQVIAN?

2. 아이큐비아ㅣ나만 몰랐던 (진짜) 포브스 선정 '세계 최고의 직장'

https://youtu.be/i8hNY49LzPs?si=Zzp2IoY4cqsD2x_e

관련 문의

한국 아이큐비아 채용(IQVIA) 카카오톡 채널을 통해 1:1 문의 하실 수 있습니다.

*채널을 추가하시면 매월 신규 포지션 알림 및 회사 소식을 받아보실 수 있습니다.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.