Clinical Research Organizations

Connecting CROs with Proven Research Professionals

Contract Research Organizations (CROs) are essential partners in accelerating clinical development on a global scale. At Planet Pharma, we support CROs in delivering full-service solutions to their clients by connecting them with top-tier talent across clinical operations, regulatory affairs, data management, biostatistics, and beyond. With deep industry expertise and an international footprint, we provide agile, tailored recruitment strategies that align with the evolving demands of CROs—helping them scale effectively, meet project timelines, and deliver excellence at every phase of the research lifecycle.

Clinical Operations Recruitment

Data Sciences Recruitment

Regulatory Affairs Recruitment

Medical Writing Recruitment

Study Start-Up Recruitment

Clinical Operations Recruitment

We source experienced professionals for critical roles in clinical operations, including:

Clinical Research Associates (CRAs)
Clinical Project Managers
Clinical Trial Coordinators
Site Manager

Our CRO recruitment experts ensure that candidates have the necessary clinical research experience and regulatory knowledge to manage site operations and execute trials successfully.

Data Sciences Recruitment

Data integrity is essential to clinical research. Planet Pharma connects CROs with skilled professionals in:

Biostatistics
Statistical Programming
Clinical Data Management
Data Science

We identify candidates with the analytical expertise required to interpret clinical trial data, ensuring accuracy, compliance, and reliability.

Regulatory Affairs Recruitment

CROs must navigate a complex regulatory landscape. Our recruitment specialists identify experts in:

Regulatory Submissions
Compliance and Quality Assurance
Health Authority Interactions

We deliver professionals who understand regulatory guidelines and can streamline approval processes, ensuring adherence to global and local regulations.

Medical Writing Recruitment

Effective medical writing is vital for regulatory submissions and study documentation. We recruit professionals skilled in:

Clinical Study Protocols
Investigator Brochures
Clinical Study Reports
Regulatory Documents

Our candidates bring both scientific expertise and technical writing skills to produce high-quality, compliant documentation.

Study Start-Up Recruitment

A smooth study start-up phase is crucial for trial success. We provide recruitment support for roles such as:

Site Contracts Specialists
Study Start-Up Managers
Clinical Trial Coordinators

Our recruitment team ensures that CROs have the right talent to initiate clinical trials efficiently, obtain approvals, and maintain compliance with protocols and timelines.