Precision for Medicine is hiring a Clinical Data Associate II to join our team. Candidates can be based in Hungary, Poland, Romania, Serbia or Slovakia. Position Summary: The Clinical Data Associate II provides data management support and assistance in all aspects of the clinical trial data management process from study start up to post database lock for assigned projects under direct supervision. Standard Operating Procedures / Work Instructions (SOPs/WIs); regulatory directives; study specific plans and guidelines will be followed. This position may perform database development and testing, as well as additional data management activities. Essential functions of the job include but are not limited to: · Support the Lead DM as a back-up and/or team member, ensuring continuity, responsiveness, and that tasks are performed in a timely manner · May perform data entry for paper-CRF studies, as needed · May perform quality control of data entry · May develop CRF specifications from the clinical study protocol and coordinate the review/feedback from all stakeholders · May assist in building clinical databases · Conduct database build UAT and maintain quality controlled database build documentation · Assist in specifying requirements for all edit check types e.g. electronic, manual data review, edit checks, etc. · Responsible for creating, revising, appropriate versioning and maintaining data management documentation. · Train clinical research personnel on the study specific CRF, EDC, and other project related items as needed · Review and query clinical trial data according to the Data Management Plan · Assist in line listing data review based on the guidance provided by the sponsor and/or Lead DM · Run patient and study level status and metric reporting · Perform medical coding of medical terms relative to each other in order to ensure medical logic and consistency · Assist with coordinating SAE/AE reconciliation · Assist with liaising with third-party vendors such as external data and EDC vendors in a project-manager capacity in support of timelines and data-related deliverables · May assist with SAS programming and quality control of SAS programs used in the Data Management department · May assist in identifying and troubleshooting operational problems, issues, obstacles, and barriers for studies based on metrics data, audit reports, and input from project team members and other stakeholders · May assist in reviewing and providing feedback on protocols, Statistical Analysis Plans (SAP) and Clinical Study Reports (CSRs), if required by the project · May assist in participating in the development and maintenance of Standard Operating Procedures (SOPs) and corresponding process documentation related to data management and database management activities · Communicate with study sponsors, vendors and project teams as needed regarding data, database or other relevant project issues · May present software demonstrations/trainings, department/company training sessions, present at project meetings · May require some travel · Perform other duties as assigned Job Qualifications: · Bachelors and/or a combination of related experience · Around 2 years’ experience working as a Clinical Data Associate for a CRO/Pharma/Biotech company. · Proficiency in Microsoft Office: Word, Excel, PowerPoint, Outlook · Able to handle a variety of clinical research tasks · Excellent organizational and communication skills · Professional use of the English language; both written and oral Precision for Medicine is the first global precision medicine clinical research services organization, purpose-built to improve the clinical research and development process for new therapeutics. Our novel approach integrates clinical operations excellence, with laboratory expertise, and advanced data sciences to inform every step. We apply our expertise to trials at all stages—from early development through approval—with embedded experience in oncology and rare disease. #LI-NC1 #LI-Remote Any data provided as a part of this application will be stored in accordance with our Privacy Policy. For CA applicants, please also refer to our CA Privacy Notice. Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law. If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at QuestionForHR@precisionmedicinegrp.com. It has come to our attention that some individuals or organizations are reaching out to job seekers and posing as potential employers presenting enticing employment offers. We want to emphasize that these offers are not associated with our company and may be fraudulent in nature. Please note that our organization will not extend a job offer without prior communication with our recruiting team, hiring managers and a formal interview process.

Precision for Medicine is hiring a Clinical Data Associate II to join our team. Candidates can be based in Hungary, Poland, Romania, Serbia or Slovakia. Position Summary: The Clinical Data Associate II provides data management support and assistance in all aspects of the clinical trial data management process from study start up to post database lock for assigned projects under direct supervision. Standard Operating Procedures / Work Instructions (SOPs/WIs); regulatory directives; study specific plans and guidelines will be followed. This position may perform database development and testing, as well as additional data management activities. Essential functions of the job include but are not limited to: · Support the Lead DM as a back-up and/or team member, ensuring continuity, responsiveness, and that tasks are performed in a timely manner · May perform data entry for paper-CRF studies, as needed · May perform quality control of data entry · May develop CRF specifications from the clinical study protocol and coordinate the review/feedback from all stakeholders · May assist in building clinical databases · Conduct database build UAT and maintain quality controlled database build documentation · Assist in specifying requirements for all edit check types e.g. electronic, manual data review, edit checks, etc. · Responsible for creating, revising, appropriate versioning and maintaining data management documentation. · Train clinical research personnel on the study specific CRF, EDC, and other project related items as needed · Review and query clinical trial data according to the Data Management Plan · Assist in line listing data review based on the guidance provided by the sponsor and/or Lead DM · Run patient and study level status and metric reporting · Perform medical coding of medical terms relative to each other in order to ensure medical logic and consistency · Assist with coordinating SAE/AE reconciliation · Assist with liaising with third-party vendors such as external data and EDC vendors in a project-manager capacity in support of timelines and data-related deliverables · May assist with SAS programming and quality control of SAS programs used in the Data Management department · May assist in identifying and troubleshooting operational problems, issues, obstacles, and barriers for studies based on metrics data, audit reports, and input from project team members and other stakeholders · May assist in reviewing and providing feedback on protocols, Statistical Analysis Plans (SAP) and Clinical Study Reports (CSRs), if required by the project · May assist in participating in the development and maintenance of Standard Operating Procedures (SOPs) and corresponding process documentation related to data management and database management activities · Communicate with study sponsors, vendors and project teams as needed regarding data, database or other relevant project issues · May present software demonstrations/trainings, department/company training sessions, present at project meetings · May require some travel · Perform other duties as assigned Job Qualifications: · Bachelors and/or a combination of related experience · Around 2 years’ experience working as a Clinical Data Associate for a CRO/Pharma/Biotech company. · Proficiency in Microsoft Office: Word, Excel, PowerPoint, Outlook · Able to handle a variety of clinical research tasks · Excellent organizational and communication skills · Professional use of the English language; both written and oral Precision for Medicine is the first global precision medicine clinical research services organization, purpose-built to improve the clinical research and development process for new therapeutics. Our novel approach integrates clinical operations excellence, with laboratory expertise, and advanced data sciences to inform every step. We apply our expertise to trials at all stages—from early development through approval—with embedded experience in oncology and rare disease. #LI-NC1 #LI-Remote Any data provided as a part of this application will be stored in accordance with our Privacy Policy. For CA applicants, please also refer to our CA Privacy Notice. Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law. If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at QuestionForHR@precisionmedicinegrp.com. It has come to our attention that some individuals or organizations are reaching out to job seekers and posing as potential employers presenting enticing employment offers. We want to emphasize that these offers are not associated with our company and may be fraudulent in nature. Please note that our organization will not extend a job offer without prior communication with our recruiting team, hiring managers and a formal interview process.

Precision for Medicine is hiring a Clinical Data Associate II to join our team. Candidates can be based in Hungary, Poland, Romania, Serbia or Slovakia. Position Summary: The Clinical Data Associate II provides data management support and assistance in all aspects of the clinical trial data management process from study start up to post database lock for assigned projects under direct supervision. Standard Operating Procedures / Work Instructions (SOPs/WIs); regulatory directives; study specific plans and guidelines will be followed. This position may perform database development and testing, as well as additional data management activities. Essential functions of the job include but are not limited to: · Support the Lead DM as a back-up and/or team member, ensuring continuity, responsiveness, and that tasks are performed in a timely manner · May perform data entry for paper-CRF studies, as needed · May perform quality control of data entry · May develop CRF specifications from the clinical study protocol and coordinate the review/feedback from all stakeholders · May assist in building clinical databases · Conduct database build UAT and maintain quality controlled database build documentation · Assist in specifying requirements for all edit check types e.g. electronic, manual data review, edit checks, etc. · Responsible for creating, revising, appropriate versioning and maintaining data management documentation. · Train clinical research personnel on the study specific CRF, EDC, and other project related items as needed · Review and query clinical trial data according to the Data Management Plan · Assist in line listing data review based on the guidance provided by the sponsor and/or Lead DM · Run patient and study level status and metric reporting · Perform medical coding of medical terms relative to each other in order to ensure medical logic and consistency · Assist with coordinating SAE/AE reconciliation · Assist with liaising with third-party vendors such as external data and EDC vendors in a project-manager capacity in support of timelines and data-related deliverables · May assist with SAS programming and quality control of SAS programs used in the Data Management department · May assist in identifying and troubleshooting operational problems, issues, obstacles, and barriers for studies based on metrics data, audit reports, and input from project team members and other stakeholders · May assist in reviewing and providing feedback on protocols, Statistical Analysis Plans (SAP) and Clinical Study Reports (CSRs), if required by the project · May assist in participating in the development and maintenance of Standard Operating Procedures (SOPs) and corresponding process documentation related to data management and database management activities · Communicate with study sponsors, vendors and project teams as needed regarding data, database or other relevant project issues · May present software demonstrations/trainings, department/company training sessions, present at project meetings · May require some travel · Perform other duties as assigned Job Qualifications: · Bachelors and/or a combination of related experience · Around 2 years’ experience working as a Clinical Data Associate for a CRO/Pharma/Biotech company. · Proficiency in Microsoft Office: Word, Excel, PowerPoint, Outlook · Able to handle a variety of clinical research tasks · Excellent organizational and communication skills · Professional use of the English language; both written and oral Precision for Medicine is the first global precision medicine clinical research services organization, purpose-built to improve the clinical research and development process for new therapeutics. Our novel approach integrates clinical operations excellence, with laboratory expertise, and advanced data sciences to inform every step. We apply our expertise to trials at all stages—from early development through approval—with embedded experience in oncology and rare disease. #LI-NC1 #LI-Remote Any data provided as a part of this application will be stored in accordance with our Privacy Policy. For CA applicants, please also refer to our CA Privacy Notice. Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law. If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at QuestionForHR@precisionmedicinegrp.com. It has come to our attention that some individuals or organizations are reaching out to job seekers and posing as potential employers presenting enticing employment offers. We want to emphasize that these offers are not associated with our company and may be fraudulent in nature. Please note that our organization will not extend a job offer without prior communication with our recruiting team, hiring managers and a formal interview process.

Precision for Medicine is hiring a Clinical Data Associate II to join our team. Candidates can be based in Hungary, Poland, Romania, Serbia or Slovakia. Position Summary: The Clinical Data Associate II provides data management support and assistance in all aspects of the clinical trial data management process from study start up to post database lock for assigned projects under direct supervision. Standard Operating Procedures / Work Instructions (SOPs/WIs); regulatory directives; study specific plans and guidelines will be followed. This position may perform database development and testing, as well as additional data management activities. Essential functions of the job include but are not limited to: · Support the Lead DM as a back-up and/or team member, ensuring continuity, responsiveness, and that tasks are performed in a timely manner · May perform data entry for paper-CRF studies, as needed · May perform quality control of data entry · May develop CRF specifications from the clinical study protocol and coordinate the review/feedback from all stakeholders · May assist in building clinical databases · Conduct database build UAT and maintain quality controlled database build documentation · Assist in specifying requirements for all edit check types e.g. electronic, manual data review, edit checks, etc. · Responsible for creating, revising, appropriate versioning and maintaining data management documentation. · Train clinical research personnel on the study specific CRF, EDC, and other project related items as needed · Review and query clinical trial data according to the Data Management Plan · Assist in line listing data review based on the guidance provided by the sponsor and/or Lead DM · Run patient and study level status and metric reporting · Perform medical coding of medical terms relative to each other in order to ensure medical logic and consistency · Assist with coordinating SAE/AE reconciliation · Assist with liaising with third-party vendors such as external data and EDC vendors in a project-manager capacity in support of timelines and data-related deliverables · May assist with SAS programming and quality control of SAS programs used in the Data Management department · May assist in identifying and troubleshooting operational problems, issues, obstacles, and barriers for studies based on metrics data, audit reports, and input from project team members and other stakeholders · May assist in reviewing and providing feedback on protocols, Statistical Analysis Plans (SAP) and Clinical Study Reports (CSRs), if required by the project · May assist in participating in the development and maintenance of Standard Operating Procedures (SOPs) and corresponding process documentation related to data management and database management activities · Communicate with study sponsors, vendors and project teams as needed regarding data, database or other relevant project issues · May present software demonstrations/trainings, department/company training sessions, present at project meetings · May require some travel · Perform other duties as assigned Job Qualifications: · Bachelors and/or a combination of related experience · Around 2 years’ experience working as a Clinical Data Associate for a CRO/Pharma/Biotech company. · Proficiency in Microsoft Office: Word, Excel, PowerPoint, Outlook · Able to handle a variety of clinical research tasks · Excellent organizational and communication skills · Professional use of the English language; both written and oral Precision for Medicine is the first global precision medicine clinical research services organization, purpose-built to improve the clinical research and development process for new therapeutics. Our novel approach integrates clinical operations excellence, with laboratory expertise, and advanced data sciences to inform every step. We apply our expertise to trials at all stages—from early development through approval—with embedded experience in oncology and rare disease. #LI-NC1 #LI-Remote Any data provided as a part of this application will be stored in accordance with our Privacy Policy. For CA applicants, please also refer to our CA Privacy Notice. Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law. If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at QuestionForHR@precisionmedicinegrp.com. It has come to our attention that some individuals or organizations are reaching out to job seekers and posing as potential employers presenting enticing employment offers. We want to emphasize that these offers are not associated with our company and may be fraudulent in nature. Please note that our organization will not extend a job offer without prior communication with our recruiting team, hiring managers and a formal interview process.