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Job Details

Lead CRA - Turkey

Company: Docs Global (Continental Europe)
Location: Turkey - Home based,Turkey
Reference: Ref AS-027479
Closing Date: 22 Feb 19
Type: Contract
Salary (£): Competitive
Benefits: Excellent & Comprehensive

Job Summary:

We offer an exciting and challenging work environment for clinical research professionals looking for an opportunity to contribute to the success of a company dedicated to researching, developing, manufacturing and marketing pharmaceuticals that improve health and quality of life.


Roles & Responsibilities of the position

• Supports the local/regional planning and execution of Client-sponsored clinical trials (phases I-IV).
• Has a comprehensive overview of all Client sponsored clinical study activities in the country or region.
• Supports or coordinates the local feasibility process of clinical programs and studies in collaboration with Clinical Operations and CRO partners, as appropriate.
• Collaborates with CROs, and Study Teams for the execution of clinical trials
• Coordinates, plans (as appropriate), attends and participates/presents at investigator meetings as appropriate.
• Subject Matter Expert on relevant local regulations and law and communicates to applicable personnel, as appropriate:
o Ensures appropriate personnel have comprehensive knowledge of relevant local regulations and laws including any amendments, as required.
• For in-sourced studies (as applicable):
o Ensures allocated studies are monitored and conducted according to protocol, SOPs/WPs and regulations (e.g. GCP/ICH, local regulations) by coordinating and supervising country CRA and CCTA, activities to ensure high quality research, timelines and expected study objectives are met.
o Manages resource utilization and tracks associated trial budgets (at local level), where applicable
o Manages / supervises EC/IRB/HA submissions / correspondence and any other local requirements to support the conduct of the clinical trial as applicable
o Oversees compliance with ICH/GCP, Client Policies, SOPs, Study Monitoring plans and local requirements
o Performs assessment visits with CRAs on assigned projects and serves as a mentor for new and junior CRAs.
o Provide oversight to direct reports to ensure clinical trial management in accordance with Corporate and local Human Resource policies, Monitoring guidelines/processes,

Job Requirements

Scientific background, you have a similar experiences in clinical research.
Ideally, experience in CRO oversight is preferred.
Strong leadership skills essential
Effective team building and teamwork skills.
Excellent written and verbal communication and interpersonal skills. Must be able to relate effectively to people at all levels of the organization
Willing to travel (around 4 times per months)
English must be fluent

Remuneration & other details

Contract: Permanent Contract with DOCS / ICON
Start date: ASAP
Home based or Office based in Ankara

Benefits: Health insurance, car allowance, mobile phone

If you are interested by this position, please send your update CV to:

About DOCS:
DOCS clients include small, mid and large sized Pharmaceutical companies in addition to many leading Biotechnology, Medical Device companies and CROs.

Key words:
CRO, Pharma, Pharmaceutical, Biotechnology, Biotech, Clinical Research Organization, Medical Device, Permanent, Contract, Clinical Research, Administrator, Assistant, CTA, Clinical Trial, Associate, Project Management, Senior, Manager, Career, Clinical Research Associates, CRA, SCRA, Clinical Monitoring, Site Monitor, Site Manager, CPM, Clinical Trial Manager, Study Director, Project Leader, Diagnostics, In-Vitro, IVD, Laboratory, Reagents, Non-interventional, Therapeutic Areas, Indication, Oncology, Respiratory, Cardiovascular, cardiology, Rheumatology, Diabetes, Ophthalmology, Dermatology, Urology, CNS, Neurology, Istanbul, Ankara, LEAD CRA, Turkey

Apply for this job: Lead CRA - Turkey

Contact Information:

Address:  Head Office
2 Globeside, Globeside Business Park
Website:  Visit Our Web Site

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