Jobs at IQVIA

• The Senior Contracts & Proposals Manager is responsible for coordinating and managing contracts, proposals, and other designated processes for assigned customers. This role ensures the delivery of accurate, compliant, and timely information while supporting complex contractual engagements. Acting as a regional subject‑matter expert, the position serves as a key customer interface and drives consistency, efficiency, and customer satisfaction across all contract and proposal activities.

Key Responsibilities

Contract & Proposal Management

• Manage day‑to‑day contract, proposal, and associated processes for large, complex, and strategic customer engagements.
• Support the development, review, and negotiation of Master Service Agreements (MSAs) and related contractual documentation.
• Ensure contractual deliverables align with customer requirements, internal policies, and applicable regulations.

Customer & Stakeholder Engagement

• Act as the primary internal point of contact for assigned customers, developing and maintaining strong, trusted relationships.
• Serve as a regional expert for contracts, proposals, and designated processes, ensuring consistency in approach, metrics, and documentation standards.
• Participate in bid defenses, customer meetings, and task forces as required.

Process Improvement & Strategy

• Identify gaps, discrepancies, and risks in project requirements and proactively engage customers and internal stakeholders to resolve issues.
• Develop, implement, and continuously improve processes with a focus on efficiency, consistency, and enhanced customer satisfaction.
• Provide strategic direction and leadership on projects and initiatives with minimal oversight.

Business & Corporate Contribution

• Actively support the achievement of corporate objectives, including revenue growth, sales enablement, and employee retention.
• Apply commercial and analytical acumen to support pricing, budgeting, and proposal development strategies.

Collaboration & Mentorship

• Provide guidance, advice, and technical support to colleagues and serve as a mentor within the contracts and proposals function.
• Maintain strong cross‑functional collaboration with Sales, Finance, Legal, Operations, and other internal teams.

Compliance & Knowledge Expertise

• Maintain in‑depth knowledge of all processes, policies, and systems related to contract and proposal development.
• Ensure full compliance with internal procedures, governance standards, and industry regulations.
• Perform additional duties as assigned.

Qualifications

Education & Experience

• Bachelor’s Degree in Life Sciences, Business Management, or a related field.
• Minimum 7 years of experience in Contracts, Proposals, or a closely related function, or an equivalent combination of education, training, and experience.
• Strong knowledge of the CRO industry.

Technical & Professional Skills

• Excellent proficiency in Microsoft Excel and Word, with a strong understanding of costing and pricing models.
• Advanced knowledge of contract, proposal, and budget development processes.
• Proven ability to interpret clinical protocols, budgets, and financial assumptions.

Competencies

• Strong analytical, organizational, and problem‑solving skills.
• Excellent verbal and written communication skills.
• Ability to build and maintain effective working relationships with customers, coworkers, and management.
• High attention to detail and ability to manage multiple complex priorities simultaneously.

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• Provides data management support, oversight and/or accountability for one or more clinical trials.
• Take the lead with the trial customer(s) and other internal and external partners to establish, align and confirm data management expectations
• Creating, planning, and tracking content, format, quality, and timing of data management deliverables, including, but not limited to, CRF, data review plan, QC plan, oversight plan, database release plan, final datasets, submission plan and archival.
• With the trial customer and other functional partners: – Gathers content and integration requirements for eCRF and other data collection tools.
• Establishes conventions and quality expectations for clinical data.
• Establishes expectations for dataset content and structure.
• Set timelines and follow-up to ensure delivery of all Data Management milestones.
• Performs trial level oversight controls, as appropriate, as described in the oversight plan, QC process and work instructions with minimal DML direction.
• Creates clinical data management documents (including submission package) ensuring appropriate quality, scientific content, organization, clarity, accuracy, format, and consistency. Ensures compliance with regulatory guidelines and the documentation matrix.
• Ensures real-time inspection readiness of all Data Management deliverables for the trial; Participate in Regulatory Agency and audits, as necessary.
• Helps plan, create and track content, format, quality, and timing of data
• management deliverables, including, but not limited to, Case Report Form, data review plan, QC plan, oversight plan, database release plan, final datasets, submission plan and archival.
• Ensures deliverables are on time.
• Participates in the assigned clinical working group(s) to ensure that Data
• Management and Therapeutic Area trial needs and deliverables are met.
• Helps Identify and communicate lessons learned, best practices and frequently asked questions at the trial level.
• Presents and trains at investigator and monitor meetings

Education/Experience

• BS/BA degree or higher preferably in Health Sciences, or BS/BA degree or higher with professional clinical experience/exposure.
• 5 years Data management experience.
• 3 years lead/co-lead experience
• Vendor Management experience
• RAVE experience

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Job Overview:

• As a Senior/Associate Principal Statistical Programmer you will provide advanced technical expertise to develop process methodology for the department to meet internal and external clients’ needs, across complex projects and studies.
• This involves planning and coordinating the development of integrated programming solutions, serving the full spectrum of statistical programming needs.
• You will provide internal consulting services, including specifications and user needs analysis for complex project or client requirements.

Key Responsibilities:

• Perform, plan co-ordinate, and implement the following for complex studies:
• The programming, testing, and documentation of statistical programs for use in creating statistical tables, figures, and listing
• The programming of analysis datasets (derived datasets) and transfer files for internal and external clients
• The programming quality control checks for the source data and to report the data issues periodically
• Ability to interpret project level requirements and develop programming specifications, as appropriate, for complex studies.
• Provide advanced technical expertise in conjunction with internal and external clients, and independently bring project solutions to SP teams
• Fulfil project responsibilities at the level of technical team lead for single complex studies or group of studies.
• Directly communicate with internal and client statisticians and clinical team members to ensure appropriate understanding of requirements and project timelines
• Estimate programming scope of work, manage resource assignments, communicate project status and negotiate/re-negotiate project timelines for deliverables
• Use and promote the use of established standards, SOP and best practices
• Provide training and mentoring to SP team members

Requirements:

• Bachelor's Degree in Maths, Computer science, Statistics, or related field
• 7+ years’ Statistical Programming experience within the Life Science Industry

Strong Efficacy experience

• Advanced knowledge of statistics, programming and/or clinical drug development process
• Advanced knowledge of computing applications such as Base SAS, SAS Graph and SAS Macro Language
• Advanced knowledge of relevant Data Standards (such as CDISC/ADaM/SDTM)

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• The role participates in all aspects of the Medical Safety activities as per scope of work.
• This includes, but is not limited to providing and maintaining of PV and risk management expertise to internal and external stakeholders, maintaining knowledge relevant to allocated product portfolios, conducting medical evaluation of post-marketing adverse drug reactions, review and contribution to signal management and benefit-risk evaluation of drugs in clinical trial and post marketing set up, preparation, and/or contribution to responses to questions from health authorities, reviewing and contributing to periodic aggregate reports, contributing to safety review of study protocols, investigators brochure and other reference safety information, and serving as an internal consultant for any medical support for pharmacovigilance operations.
• Associate Medical Safety Director

Role responsibilities:

• Providing aggregate reviews of safety information, including clinical data, to maintain oversight of a product’s safety profile
• Leads signal detection and analysis, including, signal detection strategy, frequency, and timing, reviews the Signal Detection Reports and other sources of data as applicable, raises potential signals for team discussion, contributes to safety analysis reports presentations of signal evaluation data as appropriate
• Providing medical review and contribution to IND Annual Reports, EU Periodic Benefit Risk Evaluation Reports, EU Periodic Safety Update Reports, EU Development Safety Update Reports, US Periodic Reports
• Providing medical review and contribution to Development Risk Management Plans, EU Risk Management Plans or US Risk Evaluation and Mitigation Strategies
• Review and contribute to benefit-risk evaluation of drugs in clinical trial and post marketing set up
• Providing safety oversight and contribution for label development, review, and updates
• Provide medical safety contributions to the Integrated Safety Summary or Common Technical Document
• Performing medical review and clarification of trial-related Adverse Events (AEs) and post-marketing adverse drug reactions (ADRs) including narrative content, queries, coding, expectedness, seriousness, causality, and company summary and serve as an internal consultant to pharmacovigilance case processing teams
• Representing safety and clinical data review findings during internal and external stakeholder meetings
• Providing medical safety support, contribution, and attendance at Safety Governance and other Meetings as needed
• Do you have the skills, experience and qualification required for the role:
• A medical degree from an accredited and internationally recognized medical school
• Around three years of clinical practice experience with two additional years in the pharmaceutical or associated industry, or equivalent combination of education, training and required experience
• Knowledge of applicable federal and local regulations and guidelines pertaining to clinical research including knowledge of regulations and guidelines pertaining to safety and good clinical practice and clinical trials and pharmaceutical research process
• Maintain knowledge of assigned product portfolio, therapeutic area, and recent literature
• Experience in Signal detection, Aggregate reports and Risk management.
• Capability to synthesize and critically analyze data from multiple sources and communicate complex clinical issues and analyses orally and in writing
• Ability to establish and meet priorities, deadlines, and objectives
• Demonstrated skills in contributing to multiple assignments required, capacity to work under pressure as well as initiative and flexibility and ability to adapt to changing business needs
• Ability to establish and maintain effective working relationships with coworkers, managers, and clients, including mentorship if needed

go to method of application »

• The role participates in all aspects of the Medical Safety activities as per scope of work.
• This includes, but is not limited to providing and maintaining of PV and risk management expertise to internal and external stakeholders, maintaining knowledge relevant to allocated product portfolios, conducting medical evaluation of post-marketing adverse drug reactions, review and contribution to signal management and benefit-risk evaluation of drugs in clinical trial and post marketing set up, preparation, and/or contribution to responses to questions from health authorities, reviewing and contributing to periodic aggregate reports, contributing to safety review of study protocols, investigators brochure and other reference safety information, and serving as an internal consultant for any medical support for pharmacovigilance operations.
• Associate Medical Safety Director

Role responsibilities:

• Providing aggregate reviews of safety information, including clinical data, to maintain oversight of a product’s safety profile
• Leads signal detection and analysis, including, signal detection strategy, frequency, and timing, reviews the Signal Detection Reports and other sources of data as applicable, raises potential signals for team discussion, contributes to safety analysis reports presentations of signal evaluation data as appropriate
• Providing medical review and contribution to IND Annual Reports, EU Periodic Benefit Risk Evaluation Reports, EU Periodic Safety Update Reports, EU Development Safety Update Reports, US Periodic Reports
• Providing medical review and contribution to Development Risk Management Plans, EU Risk Management Plans or US Risk Evaluation and Mitigation Strategies
• Review and contribute to benefit-risk evaluation of drugs in clinical trial and post marketing set up
• Providing safety oversight and contribution for label development, review, and updates
• Provide medical safety contributions to the Integrated Safety Summary or Common Technical Document
• Performing medical review and clarification of trial-related Adverse Events (AEs) and post-marketing adverse drug reactions (ADRs) including narrative content, queries, coding, expectedness, seriousness, causality, and company summary and serve as an internal consultant to pharmacovigilance case processing teams
• Representing safety and clinical data review findings during internal and external stakeholder meetings
• Providing medical safety support, contribution, and attendance at Safety Governance and other Meetings as needed
• Do you have the skills, experience and qualification required for the role:
• A medical degree from an accredited and internationally recognized medical school
• Around three years of clinical practice experience with two additional years in the pharmaceutical or associated industry, or equivalent combination of education, training and required experience
• Knowledge of applicable federal and local regulations and guidelines pertaining to clinical research including knowledge of regulations and guidelines pertaining to safety and good clinical practice and clinical trials and pharmaceutical research process
• Maintain knowledge of assigned product portfolio, therapeutic area, and recent literature
• Experience in Signal detection, Aggregate reports and Risk management.
• Capability to synthesize and critically analyze data from multiple sources and communicate complex clinical issues and analyses orally and in writing
• Ability to establish and meet priorities, deadlines, and objectives
• Demonstrated skills in contributing to multiple assignments required, capacity to work under pressure as well as initiative and flexibility and ability to adapt to changing business needs
• Ability to establish and maintain effective working relationships with coworkers, managers, and clients, including mentorship if needed

go to method of application »

• The role participates in all aspects of the Medical Safety activities as per scope of work.
• This includes, but is not limited to providing and maintaining of PV and risk management expertise to internal and external stakeholders, maintaining knowledge relevant to allocated product portfolios, conducting medical evaluation of post-marketing adverse drug reactions, review and contribution to signal management and benefit-risk evaluation of drugs in clinical trial and post marketing set up, preparation, and/or contribution to responses to questions from health authorities, reviewing and contributing to periodic aggregate reports, contributing to safety review of study protocols, investigators brochure and other reference safety information, and serving as an internal consultant for any medical support for pharmacovigilance operations.
• Associate Medical Safety Director

Role responsibilities:

• Providing aggregate reviews of safety information, including clinical data, to maintain oversight of a product’s safety profile
• Leads signal detection and analysis, including, signal detection strategy, frequency, and timing, reviews the Signal Detection Reports and other sources of data as applicable, raises potential signals for team discussion, contributes to safety analysis reports presentations of signal evaluation data as appropriate
• Providing medical review and contribution to IND Annual Reports, EU Periodic Benefit Risk Evaluation Reports, EU Periodic Safety Update Reports, EU Development Safety Update Reports, US Periodic Reports
• Providing medical review and contribution to Development Risk Management Plans, EU Risk Management Plans or US Risk Evaluation and Mitigation Strategies
• Review and contribute to benefit-risk evaluation of drugs in clinical trial and post marketing set up
• Providing safety oversight and contribution for label development, review, and updates
• Provide medical safety contributions to the Integrated Safety Summary or Common Technical Document
• Performing medical review and clarification of trial-related Adverse Events (AEs) and post-marketing adverse drug reactions (ADRs) including narrative content, queries, coding, expectedness, seriousness, causality, and company summary and serve as an internal consultant to pharmacovigilance case processing teams
• Representing safety and clinical data review findings during internal and external stakeholder meetings
• Providing medical safety support, contribution, and attendance at Safety Governance and other Meetings as needed
• Do you have the skills, experience and qualification required for the role:
• A medical degree from an accredited and internationally recognized medical school
• Around three years of clinical practice experience with two additional years in the pharmaceutical or associated industry, or equivalent combination of education, training and required experience
• Knowledge of applicable federal and local regulations and guidelines pertaining to clinical research including knowledge of regulations and guidelines pertaining to safety and good clinical practice and clinical trials and pharmaceutical research process
• Maintain knowledge of assigned product portfolio, therapeutic area, and recent literature
• Experience in Signal detection, Aggregate reports and Risk management.
• Capability to synthesize and critically analyze data from multiple sources and communicate complex clinical issues and analyses orally and in writing
• Ability to establish and meet priorities, deadlines, and objectives
• Demonstrated skills in contributing to multiple assignments required, capacity to work under pressure as well as initiative and flexibility and ability to adapt to changing business needs
• Ability to establish and maintain effective working relationships with coworkers, managers, and clients, including mentorship if needed

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We are seeking an experienced Oncologist to support different expanding clinical trials in solid tumors, including the addition of new study arms. This role is fully focused on clinical trial support and medical monitoring.

Key Responsibilities

• Serve as medical advisor/medical monitor for assigned oncology clinical trials
• Provide protocol guidance, inclusion/exclusion decisions, and patient safety support to study teams and investigative sites
• Perform medical review of protocols, IBs, CRFs, CSRs, AEs and SAEs
• Support safety reviews, signal evaluation, and collaboration with Pharmacovigilance
• Participate in study meetings and Investigator Meetings
• Provide timely support for urgent protocol‑related queries (per local regulations)

Requirements

• MD with formal training and relevant experience in Oncology
• 5–7+ years of experience supporting oncology clinical trials
• Strong experience in solid tumors
• Confident working in global, cross‑functional teams

go to method of application »

We are seeking an experienced Oncologist to support different expanding clinical trials in solid tumors, including the addition of new study arms. This role is fully focused on clinical trial support and medical monitoring.

Key Responsibilities

• Serve as medical advisor/medical monitor for assigned oncology clinical trials
• Provide protocol guidance, inclusion/exclusion decisions, and patient safety support to study teams and investigative sites
• Perform medical review of protocols, IBs, CRFs, CSRs, AEs and SAEs
• Support safety reviews, signal evaluation, and collaboration with Pharmacovigilance
• Participate in study meetings and Investigator Meetings
• Provide timely support for urgent protocol‑related queries (per local regulations)

Requirements

• MD with formal training and relevant experience in Oncology
• 5–7+ years of experience supporting oncology clinical trials
• Strong experience in solid tumors
• Confident working in global, cross‑functional teams

go to method of application »

We are seeking an experienced Oncologist to support different expanding clinical trials in solid tumors, including the addition of new study arms. This role is fully focused on clinical trial support and medical monitoring.

Key Responsibilities

• Serve as medical advisor/medical monitor for assigned oncology clinical trials
• Provide protocol guidance, inclusion/exclusion decisions, and patient safety support to study teams and investigative sites
• Perform medical review of protocols, IBs, CRFs, CSRs, AEs and SAEs
• Support safety reviews, signal evaluation, and collaboration with Pharmacovigilance
• Participate in study meetings and Investigator Meetings
• Provide timely support for urgent protocol‑related queries (per local regulations)

Requirements

• MD with formal training and relevant experience in Oncology
• 5–7+ years of experience supporting oncology clinical trials
• Strong experience in solid tumors
• Confident working in global, cross‑functional teams