IQVIA Posted October 12, 2026

Associate Director, Clinical Project Management

Wilayah Persekutuan Kuala Lumpur, Malaysia Full time
Clinical Development Associate Director
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IQVIA is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

Manage and support the operational elements and execution of studies and/or programs to ensure delivery; time and quality resulting in strong financial performance and customer satisfaction and in accordance with SOPs; policies and practices from pre-award to close-out. Work with study(ies)/program(s) teams to focus on leveraging deep therapeutic expertise and IQVIA solutions to drive operational excellence and strategic leadership with our customers.

Essential Functions

Participate in bid defense preparations. Lead bid defense presentations in partnership with Business Development for large sized, multiple and full service, multiple country and/or multi regional studies. Understand project strategy and operationalise the agreed upon approach.

Develop and/or support on the preparation of integrated study management plans in collaboration with the core project team.

Accountable for the strategic development and execution or delivery of clinical studies in line with agreed upon contracts while optimizing speed, quality and cost of delivery, ensuring consistent use of study tools and training materials and compliance with system updates, standard processes, policies and procedures.

Serve as primary project oversight and/or contact with customers and own relationship with the project’s key customer contact(s), communicate/collaborate with IQVIA business development representatives as necessary.;

Set objectives for the core project team according to agreed upon contract, strategy and approach, effectively communicate and assess performance, providing feedback and leadership.

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 information proactively to all stakeholders internally and externally.

Supervise problem solving and resolution efforts to include management of risk, contingencies and issues. Take accountability for proactive contingency plans to mitigate risks.

Coach and/or mentor junior team members around project delivery, planning, project review, risk management and problem solving to ensure global alignment of work practices across the team.

Achieve project quality by identifyingand proactively managing quality risks and issues, responding to issues raised by project team members and planning/implementing appropriate corrective and preventative action plans.

May participate in executive committees as part of program leadership.

Ensure the financial success of the project including optimal management and assignment of resources to achieve project goals and profitability.

Forecast and identify opportunities to accelerate activities to bring milestones and revenue forward, implement appropriate actions to achieve.;

Identify changes in scope and manage change control process, including securing customer agreement to financial and milestone updates as necessary.

Identify and communicate lessons learned and best practices to promote continuous improvement.

Adopt corporate initiatives and changes, and serve as a change advocate when necessary.

Provide input to line managers on their project team members’ performance relative to project tasks. Support staff development.

Mentor less experienced project team members on assigned projects to support their professional development.

Qualifications

Bachelor's Degree Life sciences or related field

Requires advanced knowledge of job area, and broad knowledge of a other related job areas, typically obtained through advanced education combined with experience.

Requires 10 years clinical research experience including 6 years of project management experience or equivalent combination of education, training and experience. Req

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. Good understanding of the competitive environment and how to communicate/demonstrate value through IQVIA solutions.;

Communication - Strong written and verbal communication skills including good command of English language Strong presentation skills. Requires strong negotiation and customer management skills.

Problem solving - Strong problem solving skills.

Leadership - Ability to work through others to deliver results to the appropriate quality and timeline metrics, monitoring/managing performance and providing feedback, experience productively partnering cross functionally and with customers to advance work effectively and efficiently. Ability to make decisions, bringing clarity to disparate information to inform actions and drive results.

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. Ability to work strategically to realize project goals, identifying and developing positive and compelling visions for the successful delivery of the project.

Quality - Attention to detail and accuracy in work.

Quality - Results-oriented approach to work delivery and output. Demonstrated learning agility and openness to learning and keeping own knowledge and skill set current and evolving.

IT skills - Good software and computer skills, including MS Office applications including but not limited to Microsoft Word, Excel and PowerPoint.

Collaboration - Ability to establish and maintain effective working relationships with co-workers, managers and clients. Excellent customer service skills and demonstrated ability to understand customer needs. Effective mentoring and training skills, fostering learning and knowledge sharing with colleagues.

Cross-collaboration - Ability to work across geographies displaying high awareness and understanding of cultural differences Good understanding of other IQVIA functions and their inter-relationship with Project Leadership.

Finances - Good understanding of project financials including experience managing, contractual obligations and implications.

IQVIA Core Competencies - Ability to demonstrate all IQVIA competencies (Client Focus, Collaboration, Communication, Innovation and Ownership).

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 https://jobs.iqvia.com

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.

Job details

Seniority
Associate Director
Function
Clinical Development
Therapeutic area
Not listed
Location
Wilayah Persekutuan Kuala Lumpur, Malaysia
Employment type
Full time

How this role compares

Computed from every other active Clinical Development role in our database, not just this employer's listings.

We currently track 504 comparable Associate Director Clinical Development roles across 77 biopharma companies.

504Comparable roles tracked
474Currently active
77Companies hiring similar roles
45Countries represented

Salary context

147 of 504 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject Not listed on this posting
Lowest disclosed · Sr Site Activation Coordinator · IQVIA $35,800/yr – $102,000/yr
Highest disclosed · Sr Statistical Advisor · Gilead Sciences, Inc. $261,375/yr – $338,250/yr
Peer group range $68,900 – $299,813 (median $175,600)

Where these roles are based

Top locations among the 504 comparable roles

United States222
India73
United Kingdom28
China18
Poland16
Taiwan16

+ 39 more countries

Seniority mix

504 of 504 peers have a known seniority level

Manager250
Senior143
Associate Director111

Therapeutic area mix

45 of 504 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology25
Immunology10
Neuroscience5
Ophthalmology2
Dermatology & Aesthetics1
Rare Disease1
Respiratory1

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

50%similar
IQVIA Wilayah Persekutuan Kuala Lumpur, Malaysia Senior
Same function Adjacent seniority Same country
50%similar
IQVIA Wilayah Persekutuan Kuala Lumpur, Malaysia Manager
Same function Adjacent seniority Same country
45%similar
AstraZeneca Da'an Dist., Taipei City, Taiwan Associate Director
Same function Same seniority
45%similar
AbbVie Irvine, CA Associate Director
Same function Same seniority
45%similar
AbbVie North Chicago, IL Associate Director
Same function Same seniority
45%similar
Regeneron Pharmaceuticals, Inc (USA) Remote, United States Associate Director
Same function Same seniority

Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

50%
Senior/ Site Activation Specialist
IQVIA · Wilayah Persekutuan Kuala Lumpur, Malaysia · Senior
Function Therapeutic area Adjacent seniority Country
45%
Associate Director, Aesthetics Clinical Development
AbbVie · Irvine, CA · Associate Director
Function Therapeutic area Seniority Country
45%
Associate Director, Clinical Data Management
BMS Services Sp. z o.o. · Warsaw, Poland · Associate Director
Function Therapeutic area Seniority Country
45%
Associate Director, Biostatistical Programming
Amgen Technology Pvt Ltd. · Hyderabad, India · Associate Director
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.