الرئيسية » CRA II - IVD and Clinical

CRA II - IVD and Clinical at Thermo Fisher Scientific, Inc

المنصب CRA II - IVD and Clinical
نُشر في 05 Apr 2026
انتهت الصلاحية 05 May 2026
الشركة Thermo Fisher Scientific, Inc
الموقع المملكة العربية السعودية | SA
نوع الوظيفة Full Time

الوصف الوظيفي:

أحدث معلومات الوظائف من Thermo Fisher Scientific, Inc لمنصب CRA II - IVD and Clinical. If the CRA II - IVD and Clinical الشاغرة في المملكة العربية السعودية تتوافق مع مؤهلاتك، يرجى تقديم أحدث طلب أو سيرة ذاتية مباشرة من خلال بوابة وظائف Jobkos المحدثة.

يرجى ملاحظة أن التقديم على وظيفة قد لا يكون سهلاً دائماً، حيث يجب على المرشحين الجدد استيفاء مؤهلات ومتطلبات معينة تحددها الشركة. نأمل أن تكون الفرصة المهنية في Thermo Fisher Scientific, Inc لمنصب CRA II - IVD and Clinical أدناه تتوافق مع مؤهلاتك.

Work Schedule Environmental Conditions Job Description

Join Us as a Clinical Research Associate (Level II) - IVD and Clinical - Make an Impact at the Forefront of Innovation.

We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the الأخير 5 years. As part of our global team, you'll have the opportunity to perform and coordinate all aspects of the clinical monitoring and site management process. The IVD Clinical Research Associate (CRA) is responsible for monitoring clinical trial testing sites to ensure compliance with Clinical Performance Study Protocol (CPSP), protocol, ICH GCP guidelines, SOPs, and applicable regulatory requirements. The CRA serves as the primary liaison between the clinical lead and investigational testing sites and ensures the integrity, quality, and timely delivery of IVD testing data.

As a Clinical Research Associate (Level II), you'll also conduct remote or on site visits to assess protocol and regulatory compliance and manage required documentation. You will manage procedures and guidelines from different sponsors and/or monitoring environments (i.e., FSO, FSP, Government, etc.). Acting as a site processes specialist, you will ensure that the trial is conducted in accordance with the approved protocol, ICH GCP guidelines, applicable regulations, and SOPs to guarantee subjects' rights, well being, and data reliability. You will ensure audit readiness and develop collaborative relationships with investigational sites. Detailed tasks and responsibilities assigned to your role are outlined in the task matrix.

What You'll Do
  • Perform testing site initiation, monitoring visits and close out, in accordance with the Monitoring Plan.
  • Ensure CPSP/protocol adherence and IVD safety and quality.
  • Assess adequacy of site resources, laboratory equipment, and infrastructure.
  • Monitors investigator sites with a risk based monitoring approach: applies root cause analysis (RCA), critical thinking and problem solving skills to identify site processes failure and corrective/preventive actions to bring the site into compliance and decrease risks. Ensures data accuracy through SDR, SDV and CRF review as applicable through on site and remote monitoring activities. Assess investigational product through physical inventory and records review. Documents observations in reports and letters in a timely manner using approved business writing standards. Escalates observed deficiencies and issues to clinical management expeditiously and follow all issues through to resolution. May need to maintain regular contact between monitoring visits with investigative sites to confirm that the protocol is being followed, that previously identified issues are being resolved and that the data is being recorded in a timely manner. Conducts monitoring tasks in accordance with the approved monitoring plan. Participates in the investigator payment process. Ensures a shared responsibility with other project team members on issues/findings resolution. Investigates and follows up on findings as applicable.
  • Participates in investigator meetings as necessary.
  • Identifies potential investigators in collaboration with the client الشركة to ensure the acceptability of qualified investigative sites. Initiates clinical trial sites according to the relevant procedures to ensure compliance with the protocol and regulatory and ICH GCP obligations, making recommendations where warranted. Performs trial close out and retrieval of trial materials.
  • Train testing site staff on CPSP, protocol, EDC, safety reporting, testing devices and study procedures.
  • Ensures that required essential documents are complete and in place, according to ICH GCP and applicable regulations. Conducts on site file reviews as per project specifications.
  • Provides trial status tracking and progress update reports to the Clinical Team Manager (CTM) as required. Ensures study systems are updated per agreed study conventions (e.g. Clinical Trial Management System).
  • Facilitates effective communication between investigative sites, the client الشركة and the PPD project team through written, oral and/or electronic contacts.
  • Responds to الشركة, client and applicable regulatory requirements/audits/inspections.
  • Maintains & completes administrative tasks such as expense reports and timesheets in a timely manner.
  • Contributes to the project team by assisting in preparation of project publications/tools, and sharing ideas/suggestions with team members.
  • Contributes to other project work and initiatives for process improvement, as required.
Education and Experience Requirements
  • Bachelor's degree in Microbiology or a Registered Nursing certification or equivalent and relevant formal academic / vocational qualification.
  • Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2 years as a clinical research monitor) or completion of PPD Drug Development Fellowship.
  • Valid driver's license where applicable.
  • In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.
Knowledge, Skills and Abilities
  • Proven clinical monitoring skills
  • Demonstrated understanding of medical/therapeutic area knowledge and medical terminology
  • Demonstrated ability to attain and maintain a working knowledge of ICH GCPs, applicable regulations and procedural documents
  • Well developed critical thinking skills, including but not limited to: critical mindset, in-depth investigation for appropriate root cause analysis and problem solving
  • Ability to manage Risk Based Monitoring concepts and processes
  • Good oral and written communication skills, with the ability to communicate effectively with medical personnel
  • Ability to maintain customer focus through the utilization of good listening skills, attention to detail and the ability to perceive customers' underlying issues
  • Good organizational and time management skills
  • Effective interpersonal skills
  • Attention to detail
  • Ability to remain flexible and adaptable in a wide range of scenarios
  • Ability to work in a team or independently as required
  • Good computer skills: solid knowledge of Microsoft Office and the ability to learn appropriate software
  • Fluency in Arabic and good English language and grammar skills
  • Good presentation skills
Working Conditions and Environment
  • Work is performed in an office/ laboratory/clinical/and/or الرئيسية office environment with exposure to electrical office equipment.
  • Frequent drives to site الموقعs. Frequent travel, generally 60-80% but more for some individuals. May also include extended overnight stays.
  • Exposure to biological fluids with potential exposure to infectious organisms.
  • Personal protective equipment required such as protective eyewear, garments and gloves.
  • Exposure to fluctuating and/or extreme temperatures on rare occasions

Please submit your CV in English

Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.

Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

معلومات الوظيفة:

  • الشركة: Thermo Fisher Scientific, Inc
  • المنصب: CRA II - IVD and Clinical
  • مكان العمل: المملكة العربية السعودية
  • الدولة: SA

كيفية تقديم الطلب:

بعد قراءة وفهم المعايير ومتطلبات الحد الأدنى من المؤهلات الموضحة في معلومات الوظيفة CRA II - IVD and Clinical at the office المملكة العربية السعودية أعلاه، أكمل فوراً ملفات طلب الوظيفة مثل خطاب التقديم، السيرة الذاتية، نسخة من الشهادة الجامعية، كشف الدرجات، والملاحق الأخرى كما هو موضح أعلاه. أرسلها عبر رابط الصفحة التالية أدناه.

انتهت صلاحية هذا الإعلان الوظيفي (منذ أكثر من 30 يوماً).
يرجى البحث عن أحدث فرص العمل على موقعنا الصفحة الرئيسية.

وظائف شاغرة مماثلة

  مجمع البحث عن وظائف 2026
من نحن
سياسة الخصوصية
إخلاء المسؤولية
الشروط والأحكام
اتصل بنا
إرسال ملف XML

© Jobkos

  من خلال زيارة موقع Jobkos أو عرض أو الوصول إلى أو استخدام أي من الخدمات أو المعلومات التي تم إنشاؤها أو جمعها أو تجميعها أو إرسالها إلى Jobkos، فإنك توافق على الالتزام بشروط وأحكام الخدمة التالية.
تم الإنشاء بواسطة Jobkos | | | |