IQVIA Posted October 30, 2026

Safety Associate

Dalian, China Full time
Pharmacovigilance Associate
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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

Job Overview

Manage Safety staff responsible delivering services in Safety Operations under the guidance of senior management. May contribute to Global initiatives. Work in close collaboration with Senior Management and other relevant stakeholders supporting the achievement of local and global deliverables and metrics.

Essential Functions

• Implement and support operational decisions as determined and instructed by senior management. May contribute and assist in global initiatives e.g. Change Management

• Subject Matter Expert (SME) Committees

• SOP Review Committees

• Retention, Engagement, training, processes etc.

• Assist in the implementation for measuring and improving employee engagement local and/or global actions. Maintain open and regular communication with direct reports to ensure a supportive working environment.

• Supervise Safety Operations staff in accordance with organization’s policies and applicable regulations. Responsibilities include planning, assigning, and directing work

• performance appraisal and professional development guidance

• rewarding and disciplining employees

• addressing employee relations issues

• resolving problems and absence management. Approve actions on human resources matters.

• Support the management on project resource assignments, staff hiring and staff terminations in collaborations with operations specialist managers. - Assists with staff training

• professional and career development.

• Work closely with operations managers to address problem areas, work scheduling for current and projected projects, and projected peak workloads. Monitor, assess and report utilization of staff. Identify and implement solutions to address poor utilization.

• Ensure direct reports are cross trained on Safety service offering as applicable

• monitor and develop training plans

• identify training and development needs of staff in collaboration with Training team and Safety Management.

• Lead and encourage direct reports in continuous improvement of department work processes, procedures and infrastructure. Instruct and lead direct reports in efficient management of project budgets through effective timesheet reporting. Work closely with operations specialist managers.

• Monitor and ensure that project processes and department deliverables meet expected quality, financial and productivity targets. Assist with meeting department utilization and realization targets.

• Ensure timely movement of project work through the process steps, in accordance with governing SOPs, ICH/FDA regulations and guidelines, work instructions and client expectations.

• Ensure that staff have been trained on and are following required Standard Operating Procedures (SOPs), Good Clinical Practices (GCPs), FDA and ICH guidelines and regulations, Work Instructions and project instructions.

• Work with Safety Management constructively in a matrix framework to achieve project and customer deliverables.

• Perform other duties as assigned.

• Support or Lead change management initiatives

• Effectively able to manage People issues

• Responsible for ensuring 100% compliance towards people practice and processes

Qualifications

• Bachelor's Degree Scientific or healthcare discipline or allied life sciences Req

• Bachelor's degree in life sciences or related field and up to 6 years of relevant experience, inclusive of up to 4 years of PV experience and up to 2 years of people management experience. Req

• or equivalent combination of education, training and experience. Pref

• Sound knowledge of Safety service lines. Advanced

• willingness to increase knowledge across Safety service lines and develop new skills. Advanced

• Staff management skills, effective leadership, motivational and influencing skills. Advanced

• Ability to work on multiple projects and manage competing priorities. Advanced

• Ability to mentor and coach. Advanced

• Strong presentation, report writing skills and customer focus skills. Advanced

• Ability to achieve results through communication and facilitation in a matrix service delivery environment with shared accountabilities. Advanced

• Sound judgment, decision-making and problem solving skills. Advanced

• Ability to establish and maintain effective working relationships with coworkers, managers and clients. Advanced

• Extensive use of telephone and face-to-face communication requiring accurate perception of speech. Advanced

• Regular sitting for extended periods of time. Advanced

• May require occasional travel. Advanced

• Ensure quality of deliverables according to the agreed terms. Advanced

• Demonstration of IQVIA core values while doing daily tasks. Advanced

• Skill to plan work load based on available capacity and ability to change prioritization based on workload fluctuations. Advanced

• Skill to negotiate and work on finding a central ground that is satisfactory to all concerned stake holders - Extensive use of keyboard requiring repetitive motion of fingers. Advanced

• Flexibility to operate in shifts. Advanced

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
Function
Pharmacovigilance
Therapeutic area
Not listed
Location
Dalian, China
Employment type
Full time

How this role compares

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

We currently track 37 comparable Associate Pharmacovigilance roles across 23 biopharma companies.

37Comparable roles tracked
36Currently active
23Companies hiring similar roles
20Countries represented

Salary context

4 of 37 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 · Drug Safety Associate II · Exelixis Inc $104,500/yr – $148,000/yr
Highest disclosed · Senior Manager, REMS Operations · Jazz Pharmaceuticals, Inc. $141,600/yr – $212,400/yr
Peer group range $126,250 – $177,000 (median $154,075)

Where these roles are based

Top locations among the 37 comparable roles

United States9
Germany3
France3
Japan3
Argentina2
India2

+ 14 more countries

Seniority mix

37 of 37 peers have a known seniority level

Manager23
Intern/Fellow/Postdoc9
Associate5

Therapeutic area mix

2 of 37 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology2

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 Dalian, China Intern/Fellow/Postdoc
Same function Adjacent seniority Same country
45%similar
BMS Services Sp. z o.o. Warsaw, Poland Associate
Same function Same seniority
45%similar
AstraZeneca Lisboa, Portugal Associate
Same function Same seniority
45%similar
Exelixis Inc Alameda, United States Associate
Same function Same seniority
45%similar
Exelixis Inc Remote, United States Associate
Same function Same seniority
45%similar
Sanofi R&D Vaccins City of Singapore, Singapore Associate
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.

Or follow a whole field: get every new Pharmacovigilance job in China, and choose locations and companies.

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%
Safety Operations Intern-DL 2027
IQVIA · Dalian, China · Intern/Fellow/Postdoc
Function Therapeutic area Adjacent seniority Country
45%
Drug Safety Associate II
Exelixis Inc · Alameda, United States · Associate
Function Therapeutic area Seniority Country
35%
Senior Manager PV Sweden & Affiliate Safety Representative
Mylan AB · Solna, Sweden · Manager
Function Therapeutic area Adjacent seniority Country
35%
Pharmacovigilance Operations Manager
Amgen Technology Pvt Ltd. · Hyderabad, India · Manager
Function Therapeutic area Adjacent 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.