Clinical Project Management jobs

Lead customer implementations of Tilda’s clinical trial platform, translating clinical workflows into product configurations and ensuring successful go‑live and adoption.

Responsibilities

Lead customer implementations from discovery through adoption
Conduct implementation and workflow‑discovery sessions
Develop implementation plans, workflows, milestones, and launch criteria
Coordinate implementation activities across stakeholders
Identify and mitigate implementation risks

Requirements

Nice to have: Medidata
Nice to have: Veeva
Nice to have: Oracle Clinical
Nice to have: IQVIA
Nice to have: Florence Healthcare

Skills

Clinical Trial Operations Clinical Project Management Clinical Research Project Management SaaS Platforms Medidata Veeva

Assoc. Spclst, Medical Affairs

Merck & Co., Inc. · Posted Nov 9, 2026

Open

Dublin, Leinster, Ireland
Hybrid
Contract · Associate

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Responsibilities

Bring energy, knowledge, innovation, and leadership to carry out the following:
Working on assigned projects e.g. medical education initiatives
Where appropriate and with support from the medical affairs team, play a role in identifying, developing and maintaining credible relationships with project stakeholders externally
Collaboration across Our Company’s internal functions to help the team with strategic planning process
Providing administrative support for Patient Access Programs and support development of early access processes

Requirements

Bachelor's Level 8 degree in Science, Pharmacy or related discipline

Skills

Administrative Support Business Intelligence (BI) Reporting Clinical Project Management Continuing Medical Education (CME)Data Analysis Strategic Planning

Clinical Project Manager

Rho Inc · Posted Nov 9, 2026

Open

United States
Full-time · Manager
3+ years

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Lead and manage clinical trial projects, ensuring compliance with GCP and client expectations.

Responsibilities

Lead clinical projects and cross‑functional teams
Establish and maintain project timelines and budgets
Develop and maintain project management plans
Negotiate client requests and manage scope changes
Manage project resources and vendor contracts

Requirements

Bachelor’s Degree in life sciences or public health
Nice to have: neurology
Nice to have: analgesia
Nice to have: respiratory
Nice to have: immunology

Skills

clinical project management Good Clinical Practice (GCP)vendor management budgeting risk management communication negotiation

Project Manager

ICON plc · Posted Nov 9, 2026

Open

Remote, Poland +1 more
Remote
7+ years

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Lead and coordinate clinical project activities, ensuring delivery on time, within budget, and to high quality standards.

Locations (2)

Warsaw, Mazovia, Poland
United States

Responsibilities

Develop and manage detailed clinical project plans, including timelines, budgets, and resource allocation
Lead cross‑functional project teams and facilitate effective communication
Monitor project progress, identify risks and issues, and implement mitigation strategies
Engage stakeholders to manage expectations and provide updates
Prepare and present project reports, status updates, and performance metrics to senior management

Requirements

Bachelor’s degree in life science, project management, business, or related fields
Nice to have: CNS/Rare Disease indication experience

Skills

(Sr)Clinical Trial Manager

Boehringer Ingelheim · Posted Nov 9, 2026

Open

Shanghai, Shanghai, China
On-site
Full-time · Senior
8+ years

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The Senior Clinical Trial Manager is accountable for trial activities for responsible R/OPU, ensuring compliance with GCP-ICH and local regulations while managing budgets, timelines, and site site selection.

Responsibilities

Ensure the trial is conducted in compliance with GCP-ICH, local/global regulations, applicable SOPs and according to the trial protocol by overseeing CRO and internal team activities.
Creation, management and review of the R/OPU trial budget to ensure appropriate level of financial oversight and planning accuracy.
Perform trial-specific training of R/OPU internal and external partners in line with Trial Training Plan.
Accurate planning and co-ordination of operational feasibility of trial timelines for their R/OPU.
Verify and provide input into the country and site level feasibility and OPU commitment.

Requirements

Masters degree or comparable degree
Biomedical Life Sciences

Skills

Clinical research Clinical project management GCP-ICH Clinical trial planning Scientific knowledge

Local Clinical Project Manager

IQVIA · Posted Nov 4, 2026

Open

Prague, Prague, Czech Republic
Mid
1+ years

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Leading Local Study Teams at country level to deliver committed components of clinical studies according to agreed resources, budget and timelines complying with Sponsor Procedural Documents, international guidelines such as ICH-GCP as well as relevant local regulations.

Responsibilities

Ensure overall responsibility for study commitments within the country and timely data delivery
Lead Local Study Team consisting of CRA(s), CSA(s)
Ensure compliance with Sponsor Procedural Documents, ICH-GCP and local regulations
Perform clinical and operational feasibility assessment of potential studies
Coordinate site selection process including initial Site Quality Risk Assessment and Site Qualification Visits

Requirements

Bachelor degree in related discipline, preferably in life science, or equivalent qualification

Skills

Clinical Project Management Oncology therapeutic area knowledge Clinical Study Process understanding Project management skills Czech language

Senior Project Manager

Evolution Research Group · Posted Nov 7, 2026

Open

Remote, United States
Remote
Senior
8+ years

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Senior Project Manager overseeing clinical research projects within a CRO environment

Responsibilities

Lead execution of clinical research projects ensuring regulatory compliance
Manage project scope, budget, and resources
Act as liaison between sponsor, team, and sites
Communicate progress to stakeholders and prepare presentations
Coordinate with clinical, marketing, and operations teams

Requirements

Bachelor degree in life science/healthcare

Skills

clinical project management FDA regulations GCP ICH guidelines protocol writing clinical study reports data management vendor management budgeting

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