Consultant, Clinical Project Manager – RWE

Ividata Life Sciences

. Oversee projects end to end, from setup through closeout .

Posted 11/5/2026full-timeParis • FranceMid-LevelSeniorWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in managing international clinical trials and observational studies while ensuring compliance with regulatory frameworks and data protection requirements. Proficient in coordinating cross-functional teams and managing project timelines and budgets effectively.

Highest-signal resume keywords

Clinical Project ManagementReal-World Evidence (RWE) InitiativesGood Clinical Practice (GCP/ICH)Regulatory Submissions ManagementCross-Functional Team Coordination

ATS Keywords

Tailor your resume

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills

Clinical ResearchObservational StudiesData GovernanceProject ManagementBudget ManagementTimeline ManagementMedical-Administrative DatabasesInternational Study ManagementEthics Committee SubmissionsRegulatory Compliance

Soft Skills

Detail-OrientedProactiveForward-ThinkingExcellent Interpersonal Skills

Tools & Technologies

SNDSHospital Data Warehouses

Industry Keywords

Phase I–IV Clinical TrialsGood Clinical Practice (GCP)Data Protection (GDPR)PharmDPhDMaster’s Degree in Life Sciences

Tech Stack

Tools & technologies

TypeScript

About the role

Key responsibilities & impact

Oversee projects end to end, from setup through closeout
Manage international Phase I–IV clinical trials
Manage prospective and retrospective observational studies
Lead RWE initiatives, including registries and medical-administrative databases
Coordinate local and central teams, including CRAs, clinical research technicians, data managers, biostatisticians, and data scientists
Manage vendors and CROs
Serve as the interface with Medical Affairs and Market Access departments
Ensure compliance with Good Clinical Practice (GCP/ICH)
Ensure compliance with the regulatory framework applicable to non-interventional studies
Ensure compliance with data protection requirements (GDPR)
Manage local and international ethics and regulatory submissions and formalities, including ethics committees, CNIL/CESREES, EMA, and FDA
Manage study timelines and budgets
Monitor key quality and delivery metrics, including recruitment, data completeness, and deliverables
Collaborate with IVIDATA Life Sciences teams and pharmaceutical and biotechnology clients

Requirements

What you’ll need

PharmD, PhD, or Master’s degree in life sciences, epidemiology, public health, or a related scientific discipline
Specialization in clinical research preferred
At least 3–5 years of experience in clinical project management
Proven experience working on international studies
Hands-on experience with observational, non-interventional, or RWE/RWD projects
Knowledge of the specific requirements of real-world studies, including data governance, registries, and medical-administrative databases such as SNDS or hospital data warehouses
Fluent or bilingual English required
Detail-oriented, proactive, forward-thinking, and excellent interpersonal skills
Ability to coordinate cross-functional medical, data, and biostatistics teams

Benefits

Comp & perks

Hybrid working opportunities
Stimulating, collaborative, and continuously evolving environment
High-impact assignments at the forefront of healthcare innovation
Work alongside passionate experts and leading organizations in the pharmaceutical, biotech, medical device, animal health, cosmetics, and nutrition sectors
Opportunity to contribute across the entire product lifecycle, from preclinical research through industrialization
A genuine opportunity for your ideas and expertise to make an impact across the organization