Remote Jobs RockRemote Jobs Rock

Clinical Research Associate II

📅 Sep 15
📍 🇹🇷 Ankara - Hybrid🎹 Mid-level🧫 Clinical Research Specialist📢 🇹🇷 Turkish Required📢 🇬🇧 English Required💼 Full-Time
Clinical Research MonitoringClinical Trial Site ManagementPhase II And Phase III StudiesQuality Control
Apply Now

📜 Description

  • Prepare, conduct, and report clinical monitoring visits.
  • Support quality control through compliance monitoring and report review.
  • Coordinate study progress with investigators, vendors, and support services.
  • Manage investigational products and trial supplies at clinical sites.
  • Train investigators, site staff, and project teams; prepare presentations for Investigator Meetings.
  • Support site feasibility, regulatory document collection, tracking systems, and audit follow-up.

🛠️ Requirements

  • Degree in Life Sciences (or similar), or an equivalent combination of education, training & experience
  • 2-3 years of independent on-site monitoring experience
  • Experience in all types of monitoring visits in Phase II and/or III
  • Native Turkish and full working proficiency in English (B2)
  • Experience supporting Oncology studies is beneficial, but not essential
  • Proficiency in MS Office applications
  • Ability to plan, multitask and work in a dynamic team environment
  • Communication, collaboration, and problem-solving skills
  • As you will be monitoring multiple sites, you must have a valid driver's license, and the ability to travel.
Full job description

Company Description

We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 3000 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.

Job Description

As a Clinical Research Associate II, you will work on the frontline of communication with project stakeholders, ensuring timelines, targets, and standards of clinical research projects in a variety of therapeutic indications. You will build and maintain relationships with clinical sites and investigators. You will focus on subjects’ rights, safety and well-being and quality of data compliance.

Hybrid role in Ankara, Turkey

Your responsibilities will include:

  • Preparation, conduct, and reporting of all types of monitoring visits
  • Supporting quality control, such as compliance monitoring and reports review
  • Contact for clinical investigators, vendors and support services in regard to study progress
  • Proper handling, use, accountability, reconciliation, and return of all Investigational Product(s) and trial supplies at sites
  • Delivering training of investigators, site staff and project teams
  • Be involved in site identification process and feasibility research
  • Support to Regulatory Affairs in procurement of site regulatory documents
  • Preparation and delivering of presentations at Investigator’s Meetings
  • Maintenance of study-specific automated tracking systems
  • Preparation for and attendance at company’s audits; resolution of audit findings

Qualifications

  • Degree in Life Sciences (or similar), or an equivalent combination of education, training & experience
  • 2-3 years of independent on-site monitoring experience
  • Experience in all types of monitoring visits in Phase II and/or III
  • Native Turkish and full working proficiency in English (B2)
  • Experience supporting Oncology studies is beneficial, but not essential
  • Proficiency in MS Office applications
  • Ability to plan, multitask and work in a dynamic team environment
  • Communication, collaboration, and problem-solving skills
  • As you will be monitoring multiple sites, you must have a valid driver's license, and the ability to travel. 

Additional Information

This is a great opportunity for you to further develop your skills, widen your therapeutic area experience, and become an expert in clinical research.

BillionToOne

Reporting Clinical Laboratory Scientist (RCLS)

🕒 5 days ago
BillionToOne👥 501 - 1000 employees🏢 Biotechnology

Performs high-complexity genomic data analysis and clinical reporting, interpreting sequencing results and quality metrics while troubleshooting issues and supporting technical guidance, training, and laboratory quality.

Clinical Genomic Data AnalysisNext-generation Sequencing (ngs)Bioinformatics PipelinesMolecular Diagnostics
PSI CRO

Clinical Research Associate II

🕒 12 days ago
PSI CRO👥 1001 - 5000 employees🏢 Pharmaceuticals

Conduct onsite and remote monitoring, manage site communications, and take ownership of assigned clinical studies across sponsors and therapeutic areas, supporting study quality and strong site relationships.

Clinical Research MonitoringOnsite MonitoringRemote MonitoringCRF Review
Blackbird Health

Autism Evaluator - PsyD - Contract/1099

🕒 20 days ago
Blackbird Health👥 51 - 200 employees🏢 Mental Health Care

As an Autism Evaluator, you will conduct neurodevelopmental diagnostic evaluations and provide evidence-based psychotherapy to support children and families in achieving clarity and effective care.

Neurodevelopmental Diagnostic ToolsADOS-2ASRSCARS-2
Blackbird Health

Autism Evaluator - PsyD - Contract/1099

🕒 20 days ago
Blackbird Health👥 51 - 200 employees🏢 Mental Health Care

As an Autism Evaluator, you will conduct neurodevelopmental diagnostic evaluations and provide evidence-based psychotherapy to children and families, ensuring seamless transitions into effective care.

Neurodevelopmental Diagnostic ToolsADOS-2ASRSCARS-2
PSI CRO

Clinical Research Associate II

🕒 20 days ago
PSI CRO👥 1001 - 5000 employees🏢 Pharmaceuticals

Conduct onsite monitoring and support clinical study startup, site management, and study teams across therapeutic areas while maintaining high quality standards and supporting audits, inspections, and regulatory submissions.

Onsite Clinical MonitoringStudy StartupCRF ReviewSource Document Verification

Trusted by Remote Workers