Clinical Development Analyst

About Clinergy

Clinergy Health is a boutique CRO focused on delivering high-quality, highly tailored clinical development solutions for pharmaceutical and biotech companies.

We intentionally work with a small number of strategic projects, spanning Phase I to Real-World Evidence, to ensure scientific rigor, operational excellence, and true partnership with our clients.

Our model is built on deep expertise, ownership, and human-centered performance, including a structured 4-day workweek, designed to enable sustained excellence, focus, and long-term professional development.

The Opportunity

We are looking for a high-potential Clinical Development Analyst to join our team.

This is not a traditional CRA role.

It is an unique position designed for professionals who want to expand beyond monitoring and gain broad exposure across the clinical trial lifecycle.

You will work closely with senior leaders and be actively involved in strategic, operational, and analytical aspects of clinical development, building a well-rounded foundation for future leadership roles.

What makes this role different

4-day workweek: designed to maximize productivity, learning, and well-being

Accelerated learning curve: exposure to multiple functions beyond site monitoring

High ownership environment: meaningful responsibilities from day one

Direct interaction with senior experts and clients

Key responsibilities

Study Start-Up & Project Support

Support site selection, feasibility, essential documents, and regulatory/ethics submissions follow-up

Assist in planning, tracking, and coordinating study activities

Maintain study trackers, timelines, and key documentation

Contribute to risk identification and mitigation strategies

Support on medical writing activities

Trial Conduct & Management

Support day-to-day trial execution and site communication

Track timelines, deliverables, and study milestones

Interact with sponsors, vendors, and sites

Contribute to reports, updates, and key study documentation

Support on logistics activities

On-Site Monitoring

Ensure compliance with protocol, GCP, and regulations

Review source data, essential documents, and data quality

Support sites in addressing findings and corrective actions

Required

Background in Life Sciences (e.g., Pharmacy, Biology, Biomedicine, Nursing, or related fields)

A combination of previous experience on the following will be a plus: clinical trials monitoring (CRA or similar role) for at least 1 year (mandatory), regulatory submissions, data management.

Solid understanding of GCP and clinical trial processes

Willingness to travel for on-site monitoring for eventual monitoring (around 30% of the time, but not necessarily every month).

Strong organizational skills and attention to detail

Excellent communication skills in English (written and spoken)

Self-starter profile

We are deliberately selective.

Role

This role is designed for individuals who think and operate differently and can effectively demonstrate (throughout the selection process and during the first few months on the job) alignment with Clinergy ´s operating model:

Extreme ownership mindset

You don't just "follow up", you close loops and take full responsibility for outcomes.

Intellectual honesty & clarity of thought

You are comfortable saying "I don't know, but I will figure it out quickly".

You simplify complexity and focus on what truly matters.

Obsession with quality

You aim to produce work that would stand up to the highest level of scrutiny, not just meet minimum requirements.

Structured thinking under ambiguity

You break down unclear problems into actionable steps and operate effectively without constant direction.

High learning velocity

You learn quickly and connect insights across different areas of clinical development.

Calm intensity

You perform under pressure without losing precision, judgment, or attention to detail.

Attention to detail with context awareness

You understand not only what is wrong, but why it matters and how to prevent it.

Low ego, high standards

You are open to feedback, challenge ideas constructively, and prioritize the best outcome over being right.

You move things forward proactively, while maintaining strong decision-making quality.

Genuine curiosity about clinical development

You seek to understand how and why studies are designed, executed, and interpreted in order to be able to connect the dots, not just perform tasks.

Why Join Clinergy Health?

Broader role than a traditional CRA position, with exposure to strategic and project-level activities.

Balanced travel model, avoiding the heavy travel burden typical of monitoring-only roles;

Close collaboration with highly experienced clinical development professionals;

High scientific and regulatory standards, with real ownership of your work;

Highly competitive compensation rates.

If you are looking to grow beyond monitoring, gain a deeper understanding of how clinical trials are planned and managed, and work in a focused, high-quality CRO environment, we would be happy to hear from you.

Applications: online via LinkedIn advertisement or by sending your resume to ******

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