Clinical Research Associate II at PSI CRO

Ankara, Ankara, Turkey -

Full Time

Start Date

Immediate

Expiry Date

22 Jul, 26

Salary

0.0

Posted On

23 Apr, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical research, Monitoring visits, Regulatory affairs, Oncology, Data compliance, Investigator training, Site management, Project tracking, MS Office, Communication, Problem-solving, Collaboration, Feasibility research, Quality control

Industry

Pharmaceutical Manufacturing

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 (6 months office-based, followed by a hybrid work model) 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 1 year 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.

Responsibilities

The role involves conducting and reporting clinical monitoring visits while ensuring data quality and compliance with regulatory standards. You will also serve as the primary point of contact for investigators and vendors to manage study progress and site relationships.