Cra

hace 6 meses

Ciudad de México Thermo Fisher Scientific A tiempo completo

Bachelor's degree in a life sciences related field or a Registered Nursing certification or equivalent and relevant formal academic / vocational qualification.

Minimal clinical monitoring experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2 years) in a clinical environment where experience is gained in clinical trials, medical terminology, medical research, clinical research or health care or experience in a health sciences field with formal training in medical terminology and anatomy may be considered. Valid driver's license where applicable.

Knowledge, Skills and Abilities:

- Basic medical/therapeutic area knowledge and understanding of medical terminology.
- Ability to attain and maintain a working knowledge of ICH GCPs and applicable regulations and procedural documents.
- Good oral and written communication skills, with the ability to communicate effectively with medical personnel.
- Good interpersonal skills
- 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
- Ability to remain flexibile and adaptable in a wide range of scenarios.
- 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.
- 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.

Good English language and grammar skills

Management Role: No management responsibility

Working Conditions and Environment:

- Work is performed in an office/ laboratory/clinical/and/or home office environment with exposure to electrical office equipment.
- Frequent drives to site locations. 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.

Physical Requirements:

- Ability to work in an upright and /or stationary position for 6-8 hours per day.
- Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists.
- Frequent mobility required.
- Occasional crouching, stooping, with frequent bending and twisting of upper body and neck.
- Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs.
- Ability to access and use a variety of computer software developed both in-house and off-the-shelf.
- Ability to communicate complex information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences.
- Frequently interacts with others to obtain or relate information to diverse groups.
- Performs a wide range of variable tasks as dictated by variable demands and changing conditions with little predictability as to the occurrence. Ability to perform under stress. Ability to multi-task.
- Regular and consistent attendance.

Qualifications:
Education and Experience:
High / Secondary school diploma or equivalent and relevant formal academic / vocational qualification.

Bachelor's degree preferred.

Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 0 to 1 year).

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.

  • Cra Manager

    hace 5 meses

    Ciudad de México MSD A tiempo completo

    **Job Description**: This role will be key to ensure strong monitoring in our clinical trials. Under the oversight of the Head of Site Management and Monitoring, the person is responsible to manage a team of 6-14 CRAs and to ensure excellent study and site performance with strict adherence to local regulations, company teams As line manager the role is...

  • Cra Ii

    hace 6 meses

    Ciudad de México ICON plc A tiempo completo

    **Experienced CRA - Mexico City, home-based role** ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of...

  • Clinical Research Associate

    hace 1 mes

    Ciudad de México, Ciudad de México Thermo Fisher Scientific A tiempo completo

    Job SummaryThermo Fisher Scientific is seeking a highly skilled Clinical Research Associate (CRA) to join our team. As a CRA, you will be responsible for monitoring investigator sites with a risk-based approach, applying root cause analysis and critical thinking skills to identify site processes failures and corrective/preventive actions. You will ensure...

  • Cra Line Manager

    hace 1 mes

    Ciudad de México, CDMX Novo Nordisk A tiempo completo

    CRA Line Manager **Category**:Clinical Development**Location**:Ciudad de México, Ciudad de México, MX- **Position Description** As a CRA Line Manager at Novo Nordisk, you will: - Manage a team of CRAs to ensure compliance with ICH/GCP, SOPs, and local regulations. - Oversee resource allocation and monitor staff utilization for clinical projects in the...

  • Ssu Cra

    hace 6 meses

    Ciudad de México Novartis A tiempo completo

    Site relationship management role to ensure sustainable trial start-up at Site. The Study Start-Up CRA is accountable for site selections as well as study-specific start-up activities and deliverables of assigned sites for Phase I-IV GDD trials within the country in adherence with monitoring procedures and processes in accordance with ICH/GCP, local...

  • Clinical Research Associate

    hace 4 semanas

    Ciudad de México, Ciudad de México Thermo Fisher Scientific A tiempo completo

    Job Summary: We are seeking a highly motivated and detail-oriented Clinical Research Associate (CRA) to join our team at Thermo Fisher Scientific. The successful candidate will be responsible for monitoring investigator sites to ensure compliance with regulatory requirements and good clinical practices.Key Responsibilities:Conduct risk-based monitoring at...

  • Cra Ii or Sr Cra Oncology

    hace 5 meses

    Edo. de México Syneos Health Clinical A tiempo completo

    **Description** **CRA II or Sr CRA oncology & on site experience Home Based Mexico** **CDMX/Aguascalientes/Oaxaca/Guadalajara - availability to travel required** Syneos Health is the only fully integrated biopharmaceutical solutions organization purpose-built to accelerate customer success. We lead with a product development mindset, seamlessly connecting...

  • Cra Ii or Sr Cra Assigned to Client Cdmx/gdl/mty

    hace 5 meses

    Edo. de México Syneos Health Clinical A tiempo completo

    **Description** **CRA II or SR CRA assigned to client CDMX/GDL/MTY** Syneos Health is the only fully integrated biopharmaceutical solutions organization purpose-built to accelerate customer success. We lead with a product development mindset, seamlessly connecting our capabilities to add high-value insights to speed therapies to patients and provide...

  • Cra Ii

    hace 5 meses

    Ciudad de México ICON A tiempo completo

    As a Clinical Research Monitor you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. **What you will be doing**: The Clinical Research Associate (CRA) monitors the progress of clinical studies at investigative sites or remotely, ensuring clinical trials are conducted, recorded, and...

  • Cfsp Cra 1

    hace 5 meses

    Ciudad de México Novasyte A tiempo completo

    Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions - Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance...

  • Sr Cra

    hace 6 meses

    Ciudad de México Thermo Fisher Scientific A tiempo completo

    PPD’s mission is to improve health. It starts as an idea to find a cure. It becomes a life saved. All in-between, it’s you! We know that meaningful results not only require the right approach, but also the right people. We invite you to re-imagine health promoting protocols with us, working alongside our talented, bright and energetic teams. Our global...

  • Cra (Level I)

    hace 6 meses

    Ciudad de México Thermo Fisher Scientific A tiempo completo

    CRA (LeveI I) Bachelor's degree in a life sciences related field or a Registered Nursing certification or equivalent and relevant formal academic / vocational qualification. Minimal clinical monitoring experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2 years) in a clinical environment where experience is...

  • Cra

    hace 6 meses

    Ciudad de México Thermo Fisher Scientific A tiempo completo

    Essential Functions- 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...

  • Clinical Research Associate

    hace 4 semanas

    Ciudad de México, Ciudad de México Thermo Fisher Scientific A tiempo completo

    Clinical Research Associate Job DescriptionPurpose:Clinical Research Associate (CRA) Job SummaryWe are seeking a highly motivated and detail-oriented Clinical Research Associate (CRA) to join our team. The CRA will be responsible for monitoring and coordinating clinical trials, ensuring compliance with regulatory requirements and Good Clinical Practice (GCP)...

  • Clinical Research Associate

    hace 1 semana

    Ciudad de México, Ciudad de México Thermo Fisher Scientific A tiempo completo

    Job SummaryWe are seeking a highly skilled Clinical Research Associate to join our team. As a CRA, you will be responsible for ensuring compliance with regulatory requirements and guidelines in the conduct of clinical trials.

  • Cra I/ii/senior with Experience On Site Any

    hace 2 semanas

    México, Méx. Syneos - Clinical and Corporate - Prod A tiempo completo

    **Description** **CRA any level with previous experience on-site any therapeutic area - sponsor dedicated Home Based CDMX** Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market...

  • Clinical Research Associate

    hace 6 meses

    Ciudad de México MSD A tiempo completo

    **Job Description**: The role is accountable for performance and compliance for assigned protocols and sites in a country. Under the oversight of the CRA manager the person ensures compliance of study conduct with ICH/GCP and country regulations, policies and procedures, quality standards and adverse event reporting requirements internally and...

  • Clinical Research Manager

    hace 1 mes

    Ciudad de México, Ciudad de México PSI A tiempo completo

    Job Title: Lead CRAAbout the RoleWe are seeking a highly skilled and experienced Lead Clinical Research Associate to join our team at PSI. As a Lead CRA, you will play a key role in managing local Monitors, supervising clinical monitoring and site management activities to ensure the protection of trial subjects' rights, safety, and well-being, data quality,...

  • Cra 2

    hace 5 meses

    Ciudad de México Novasyte A tiempo completo

    Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions - Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance...

  • Cra

    hace 5 meses

    México Thermo Fisher Scientific A tiempo completo

    Bachelor's degree in a life sciences related field or a Registered Nursing certification or equivalent and relevant formal academic / vocational qualification. Minimal clinical monitoring experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2 years) in a clinical environment where experience is gained in clinical...