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CRA II - Single Sponsor

RBW Consulting
Turkey (TR)
900k - 1MIL plus company car
Start date
21 May 2024
Closing date
20 Jun 2024

Job Details

  • Title: CRA II
  • Company: FSP/Single Sponsor – top pharmaceutical company
  • Location: Remote (Ankara/Istanbul, Turkey) 
  • Salary: 1MIL - 1.5MIL TRY
  • Benefits: Company car or car allowance, medical insurance, healthcare, meal vouchers, and more


RBW Consulting are excited to announce an opportunity on behalf of one of our close clients. This company are a renowned CRO with leading healthcare intelligence and a European culture. They treat unmet disease target areas and advance clinical research by providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organizations.


They are looking for an experienced CRA with 1.5+ years’ experience to join one of their admired pharmaceutical clients within a fully embedded position. Here, you will have the chance to work with a consistent set of SOPs and systems, gain more insight into the full drug development process, and work with top of the range blockbuster medicines. This also means you will have more time to respond to site queries, follow up with your trip reports, and have a more quality driven approach to you research. Therapy areas available to work on include but are not limited to oncology, haematology, infectious diseases, vaccines, neurology, nephrology, ophthalmology, CNS, and rare diseases.


Travel is national but it is possible to have sites assigned that are closer to your residence. The position is fully remote when not visiting sites. This is a great opportunity to feel part of an admired pharmaceuticals clinical research team and join an organization that helps its employees grow towards CTL/CTM positions within a 12 to 36 month period (depending on performance).


Key accountabilities:

  • Autonomy of investigator sites with full responsibility for the successful management of sites through study life cycle (start-up to close-out);
  • Conduct feasibility, pre-study, initiation, monitoring, and closeout visits for research sites, mainly phase 1 to 3 and within all available therapeutic areas;
  • Prepare accordingly and attend investigator meetings, coordinating timely delivery and subsequent proper storage and accountability of clinical supplies and following-up of drug safety issues;
  • Perform source document verification and case report form review;
  • Perform regulatory document review;
  • Conduct study drug inventory;
  • Perform adverse event and serious adverse event reporting and follow-up; and
  • Assess patient recruitment and retention.



  • Minimum 3+ years independent monitoring experience
  • Excellent written and verbal communication skills to express complex ideas to study personnel at research and clinical institutions.
  • Excellent organizational and interpersonal skills.
  • Ability to interact with all levels of staff to coordinate/execute study activities.
  • Ability to handle several priorities within multiple, complex clinical trials.
  • Ability to reason independently and recommend specific solutions in clinical settings.
  • Able to mentor other CRAs on project team and co-monitor as required.
  • Understanding of basic data processing functions, including electronic data capture.
  • Understanding of current GCP/ICH guidelines applicable to the conduct of clinical research.



  • Competitive salary and company car or car allowance
  • Other social benefits such as competitive annual leave, pension, and healthcare
  • Embedded to one client - consistent SOPs and processes
  • Quality driven approach
  • More time to respond to site queries and follow up with trip reports
  • Access to vertical/horizontal growth (can become CTL/CTM in 12 to 26 months depending on performance)
  • Access to blockbuster drugs and/or biosimilars
  • Feeling a part of a collaborative team within pharma industry


To apply:

If you would like to discuss this vacancy further or to discuss your career options in confidence, please telephone on +44 (0) 1273 049 215


Please click ‘apply’ or contact Joe Pearce for any further information


About RBW Consulting

RBW Consulting is a life sciences talent & strategic consultancy with purpose, delivered through what we call Human Intelligence. We help life sciences businesses change the world by giving them the people, insight & networks to innovate and scale. We are proud of our role in helping companies deliver better health and wellbeing outcomes for patients We give back by playing an active role in funding initiatives that change lives We’ve created a culture rooted in support, transparency and mutual commitment. We lead with our values from the inside; empowering and investing in our people is more important than short-term commercial gain.


We are an equal opportunities Recruitment Business and Agency

RBW Consulting is an equal opportunity workplace. We prioritize talent (both current and potential) over resumes, challenge the status quo, and value people as our most important asset. We do not discriminate on the basis of race, ethnicity, colour, sex, gender identity or expression, sexual orientation, religion, age, marital status, visible or invisible disability, medical condition, national origin, veteran status, or any other protected status. We strive to be a diverse workforce that is representative at all levels and are committed to building a team that represents a variety of backgrounds, perspectives, and skills.


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