Clinical Research Associate Ii

3 weeks ago

Mumbai, India Fortrea - Organic Full time

C. Essential Job Duties:
 The below statements are intended to describe the general nature of the job and are not intended to be an exhaustive list of all responsibilities, skills and duties.

 Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned

 Responsible for all aspects of site management as prescribed in the project plans

 General On-Site Monitoring Responsibilities

 Ensure the study staff who will conduct the protocol have received the proper materials and instructions to safely enter patients into the study

 Ensure the protection of study patients by verifying that informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements

 Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document review

 Monitor data for missing or implausible data

 Ensure the resources of the Sponsor and Labcorp are spent wisely by performing the required monitoring tasks in an efficient manner, according to SOPs and established guidelines, including managing travel expenses in an economical fashion according to Labcorp travel policy

 Ensure audit readiness at the site level

 Travel, including air travel, may be required and is an essential function of the job.

 Prepare accurate and timely trip reports

 Responsible for all aspects of registry management as prescribed in the project plans

 Undertake feasibility work when requested

 Participate in and follow up on Quality Control Visits (QC) when requested

 Recruitment of potential investigators, preparation of EC submissions, notifications to regulatory authorities, translation of study-related documentation, organization of meetings and other tasks as instructed by supervisor

 Might be requested to work in a client facing environment

 Track and follow up on Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAE

 Independently perform CRF review; query generation and resolution against established data review guidelines on Labcorp or client data management systems as assigned by management

 Assist with training, of new employees, e.g. co-monitoring

 Coordinate designated clinical projects as a Local Project Coordinator (with supervision, if applicable), and may act as a local client contact as assigned

 Perform other duties as assigned by management

**Experience**:
Minimum Required:
 2 - 3 years of Clinical Monitoring experience is preferred, or an equivalent combination of education and experience to successfully perform the key responsibilities of the job can be substituted.

 Ability to monitor study sites independently according to protocol monitoring guidelines, SOP, and local regulatory Guidelines

 Have a full understanding of the Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs

 Good planning, organization, and problem
- solving abilities

 Ability to work with mínimal supervision

 Good communication and interpersonal skills

 Good analytical and negotiation skills

 Computer competency

 Fluent in local office language and in English, both written and verbal

 Works efficiently and effectively in a matrix environment

Preferred:
 1 - 2 years of onsite monitoring experience in Oncology, Neurology, Ophthalmology and Cardiology studies is preferred, however an equivalent combination

Fortrea is proud to be an Equal Opportunity Employer:
As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.

For more information about how we collect and store your personal data, please see our

Privacy Statement

.

  • Clinical Research Associate Ii

    2 weeks ago

    Navi Mumbai, India Labcorp Full time

    **Job Summary**: The Clinical Research Associate II (CRA II) is responsible and accountable for site monitoring and site management. Has responsibility for clinical studies according to Company, and/or Sponsor Standard Operating Procedures, and local regulatory guidelines. Assures the implementation of project plans, as assigned. Act in the project role of a...

  • Clinical Research Faculty

    2 weeks ago

    Borivali, Mumbai, Maharashtra, India Clinomic Center For Clinical research Full time

    all Clinical Research Topic: - DRUG DEVELOPMENT: FROM MOLECULE TO PRESCRIPTION: PART 1 DRUG DEVELOPMENT: FROM MOLECULE TO PRESCRIPTION: PART 2 THE EVALUTION OF THE CLINICAL TRIAL PROCESS-A BRIEF HISTORY LESSON HISTORICAL BACKGROUND OF GCPINSTITUTIONAL REVIEW BOARD/INDEPENDENT ETHICS COMMITTEE (IRB/IEC)STAKEHOLDERS ENGAGEMENT TO ENSURE A SUCCESSFUL TRIAL...

  • Clinical Research Associate

    2 weeks ago

    Mumbai, Maharashtra, India REGROW BIOSCIENCES Full time

    About the company and the position:Hey there! Are you a Clinical Research Associate (CRA) looking for an exciting opportunity to be a key player in clinical trials? Well, look no further! Join our team and be a crucial part of the development and execution of cutting-edge clinical research. Here's what you'll be doing:Responsibilities: Assist in developing...

  • Clinical Research Associate

    1 month ago

    Mumbai, India REGROW BIOSCIENCES Full time

    Overview: As a Clinical Research Associate (CRA), you will play a pivotal role in the development and execution of clinical trials Working closely with research teams, regulatory bodies, and clinical sites, you will ensure compliance with protocols, regulatory requirements, and industry standards throughout the trial process. Responsibilities: 1 . Trial...

  • Clinical Research Associate

    3 months ago

    mumbai, India REGROW BIOSCIENCES Full time

    Overview:As a Clinical Research Associate (CRA), you will play a pivotal role in the development and execution of clinical trials Working closely with research teams, regulatory bodies, and clinical sites, you will ensure compliance with protocols, regulatory requirements, and industry standards throughout the trial process.Responsibilities:1 . Trial...

  • Clinical Research Associate

    4 weeks ago

    mumbai, India REGROW BIOSCIENCES Full time

    Overview:As a Clinical Research Associate (CRA), you will play a pivotal role in the development and execution of clinical trials Working closely with research teams, regulatory bodies, and clinical sites, you will ensure compliance with protocols, regulatory requirements, and industry standards throughout the trial process.Responsibilities:1 . Trial...

  • Clinical Research Associate

    3 months ago

    Mumbai, India REGROW BIOSCIENCES Full time

    Overview:As a Clinical Research Associate (CRA), you will play a pivotal role in the development and execution of clinical trials Working closely with research teams, regulatory bodies, and clinical sites, you will ensure compliance with protocols, regulatory requirements, and industry standards throughout the trial process.Responsibilities:1.Trial...

  • Clinical Research Associate

    3 months ago

    Mumbai, India REGROW BIOSCIENCES Full time

    Overview:As a Clinical Research Associate (CRA), you will play a pivotal role in the development and execution of clinical trials Working closely with research teams, regulatory bodies, and clinical sites, you will ensure compliance with protocols, regulatory requirements, and industry standards throughout the trial process.Responsibilities:1.Trial...

  • Clinical Research Associate

    3 months ago

    Mumbai, India REGROW BIOSCIENCES Full time

    Overview: As a Clinical Research Associate (CRA), you will play a pivotal role in the development and execution of clinical trials Working closely with research teams, regulatory bodies, and clinical sites, you will ensure compliance with protocols, regulatory requirements, and industry standards throughout the trial process. Responsibilities: 1 . Trial...

  • Clinical Research Associate

    2 weeks ago

    Mumbai, Maharashtra, India REGROW BIOSCIENCES Full time

    Overview:As a Clinical Research Associate (CRA), you will play a pivotal role in the development and execution of clinical trials Working closely with research teams, regulatory bodies, and clinical sites, you will ensure compliance with protocols, regulatory requirements, and industry standards throughout the trial processResponsibilities:1 Trial...

  • Clinical Research Associate

    4 weeks ago

    Mumbai, India REGROW BIOSCIENCES Full time

    Overview:As a Clinical Research Associate (CRA), you will play a pivotal role in the development and execution of clinical trials Working closely with research teams, regulatory bodies, and clinical sites, you will ensure compliance with protocols, regulatory requirements, and industry standards throughout the trial process.Responsibilities:1.Trial...

  • Clinical Research Associate

    4 weeks ago

    Mumbai, India REGROW BIOSCIENCES Full time

    Overview:As a Clinical Research Associate (CRA), you will play a pivotal role in the development and execution of clinical trials Working closely with research teams, regulatory bodies, and clinical sites, you will ensure compliance with protocols, regulatory requirements, and industry standards throughout the trial process.Responsibilities:1.Trial...

  • Clinical Research Associate

    4 weeks ago

    Mumbai, India REGROW BIOSCIENCES Full time

    Overview: As a Clinical Research Associate (CRA), you will play a pivotal role in the development and execution of clinical trials Working closely with research teams, regulatory bodies, and clinical sites, you will ensure compliance with protocols, regulatory requirements, and industry standards throughout the trial process. Responsibilities: 1 . Trial...

  • Clinical Research Associate

    2 weeks ago

    Mumbai, Maharashtra, India Novo Nordisk Full time

    Department: Clinical Development CentreDo you want to be a part of a high performing team in Novo Nordisk that plays a critical role in driving the success of the business? Do you have what it takes: the right drive, a sharp mind, customer orientation, openness and focus on what matters and a genuine interest in working with people? If you find challenges...

  • Clinical Research Associate

    2 weeks ago

    Mumbai, India Statistical Pharma Full time

    Specific duties can vary depending on the company, but clinical research associates will generally be required to: - Develop trial procedures, methodology and instructions for clinical trials staff, as well as design data collection tools (case report forms) - Manage study supplies, drug supplies and drug accountability (and prepare study drugs for...

  • Clinical Research Associate

    4 weeks ago

    Mumbai, India BIORASI LLC Full time

    **We are Growing**! Let us support your career journey the Biorasi way. Innovative, Collaborative, Dynamic and Evolving. Capitalizing on your strengths while encouraging work-life balance. Biorasi is an award-winning, customer-focused, full-service clinical research organization, and we are unlike any CRO you’ve ever heard of. Biorasi is looking for top...

  • Clinical Research Coordinator

    3 months ago

    Mumbai, India Learning Labb Research Institute Full time

    We are seeking a motivated and detail-oriented Clinical Research Coordinator to join our dynamic team. As a Clinical Research Coordinator, you will play a crucial role in the planning, implementation, and coordination of clinical research studies. You will work closely with principal investigators, study participants, and other healthcare professionals to...

  • Clinical Research Coordinator

    3 months ago

    Mumbai, India Learning Labb Research Institute Full time

    We are seeking a motivated and detail-oriented Clinical Research Coordinator to join our dynamic team. As a Clinical Research Coordinator, you will play a crucial role in the planning, implementation, and coordination of clinical research studies. You will work closely with principal investigators, study participants, and other healthcare professionals to...

  • Clinical Research Associate

    3 weeks ago

    Navi Mumbai, Maharashtra, India Medpace, Inc. Full time

    Job Summary: Our successful Clinical Research Associates possess varied backgrounds in medical and other science-related healthcare fields. Individuals who have succeeded in the CRA role include: - Nurses - Dieticians - Pharmacy Technicians - Pharmaceutical/Device Sales Representatives - Biotech Engineers - Health and Wellness Coordinators - Research...

  • Experienced Clinical Research Associate

    3 weeks ago

    Navi Mumbai, Maharashtra, India Medpace, Inc. Full time

    Job Summary: Our successful Clinical Research Associates possess varied backgrounds in medical and other science-related healthcare fields. Individuals who have succeeded in the CRA role include: - Nurses - Dieticians - Pharmacy Technicians - Pharmaceutical/Device Sales Representatives - Biotech Engineers - Health and Wellness Coordinators - Research...