Clinical Research Assistant

HOT JOB - IMMEDIATE OPENING!

Culmen International is seeking a Clinical Research Assistant to work in Manila, Philippines.

This position will provide support in clinical areas for research purposes in WRAIR-AFRIMS.

• Screens subjects for eligibility to participate in research protocols, enrolls subjects and obtains informed consent
• Performs study procedures as required, such as specimen collection of respiratory, blood and stool samples
• Performs initial procedures such as rapid tests
• Labels, transports and stores specimens, and assists in shipments
• Collects and records data onto Case Report
• Reviews study-related documents and ensures data completeness, accuracy, and security.
• Schedules and performs follow-up visits with study
• Performs regular quality control checks on data, and reporting any problems or inconsistencies
• Maintains accurate records of interviews, safeguarding the confidentiality of subjects as necessary
• Ensures that target population of the study would be achieved.
• Provide ready access to all experimental data for the Principal Investigator and/or supervisor
• Requests or acquires supplies necessary for the project
• Manages and responds to project-related email
• Codes and verifes data in accordance with specified research protocol and coding procedures and enter data into a computer database and/or spreadsheet application for subsequent analysis
• Assists Clinical Investigators in planning and execution of research
• Manage the regulatory documents and prepare study files for inspections and audits.
• Serves as liaison between WRAIR-AFRIMS Philippines and collaborators
• Coordinates with WRAIR-AFRIMS Philippines, Cebu Senior Clinical Research coordinator for guidance regarding regulatory requirements (if required)
• Prepares study documents that serve as source documents for the study
• Prepares the project site for monitoring visits.
• Assists in preparing progress reports, to include Continuing Review Reports
• Coordinates with the Principal Investigator in training of study staff in the conduct of the research study as defined by the approved protocol, SOPs and SSPs related to the study
• Provide regular feedback to study personnel
• Establishes performance measures so as to monitor the progress of the research project
• Ensures that studies are conducted in accordance with approved protocols, institutional regulatory requirements, SOPs, SSPs, Good Clinical Practice (GCP) guidelines, sponsor guidelines and other regulatory requirements as applicable
• Performs other duties as assigned by his/her direct supervisor or her designee
• Bachelor’s degree in Nursing or related field
• Previous research experience (e.g. performing subject consent, data collection, team collaboration) for at least 2 years is an advantage
• Strong written and verbal communication skills
• Excellent interpersonal skills and team player
• High attention to detail in data collection, entry, and analysis
• Strong organizational skills with ability to prioritize tasks and meet deadlines
• Knowledge of ethical guidelines and IRB protocols (if applicable)
• Familiarity with research/medical terminology and scientific methods
• Capable of handling administrative tasks and documentation
• Motivated, results-driven, and proactive
• Proficient in MS Office and Windows-based softwares
  
  
  

Culmen International is committed to enhancing international safety and security, strengthening homeland defense, advancing humanitarian missions, and optimizing government operations. With experience in over 150 countries, Culmen supports our clients to accomplish critical missions in challenging environments.

To learn more about Culmen International, please visit www.culmen.com.

At Culmen International, we are committed to creating and sustaining a workplace that upholds the principles of Equal Employment Opportunity (EEO). We believe in the importance of fair treatment and equal access to opportunities for all employees and applicants. Our commitment to these principles is unwavering across all our operations worldwide.

HOT JOB - IMMEDIATE OPENING!

Culmen International is seeking a Clinical Research Assistant to work in Manila, Philippines.

This position will provide support in clinical areas for research purposes in WRAIR-AFRIMS.

• Screens subjects for eligibility to participate in research protocols, enrolls subjects and obtains informed consent
• Performs study procedures as required, such as specimen collection of respiratory, blood and stool samples
• Performs initial procedures such as rapid tests
• Labels, transports and stores specimens, and assists in shipments
• Collects and records data onto Case Report
• Reviews study-related documents and ensures data completeness, accuracy, and security.
• Schedules and performs follow-up visits with study
• Performs regular quality control checks on data, and reporting any problems or inconsistencies
• Maintains accurate records of interviews, safeguarding the confidentiality of subjects as necessary
• Ensures that target population of the study would be achieved.
• Provide ready access to all experimental data for the Principal Investigator and/or supervisor
• Requests or acquires supplies necessary for the project
• Manages and responds to project-related email
• Codes and verifes data in accordance with specified research protocol and coding procedures and enter data into a computer database and/or spreadsheet application for subsequent analysis
• Assists Clinical Investigators in planning and execution of research
• Manage the regulatory documents and prepare study files for inspections and audits.
• Serves as liaison between WRAIR-AFRIMS Philippines and collaborators
• Coordinates with WRAIR-AFRIMS Philippines, Cebu Senior Clinical Research coordinator for guidance regarding regulatory requirements (if required)
• Prepares study documents that serve as source documents for the study
• Prepares the project site for monitoring visits.
• Assists in preparing progress reports, to include Continuing Review Reports
• Coordinates with the Principal Investigator in training of study staff in the conduct of the research study as defined by the approved protocol, SOPs and SSPs related to the study
• Provide regular feedback to study personnel
• Establishes performance measures so as to monitor the progress of the research project
• Ensures that studies are conducted in accordance with approved protocols, institutional regulatory requirements, SOPs, SSPs, Good Clinical Practice (GCP) guidelines, sponsor guidelines and other regulatory requirements as applicable
• Performs other duties as assigned by his/her direct supervisor or her designee
• Bachelor’s degree in Nursing or related field
• Previous research experience (e.g. performing subject consent, data collection, team collaboration) for at least 2 years is an advantage
• Strong written and verbal communication skills
• Excellent interpersonal skills and team player
• High attention to detail in data collection, entry, and analysis
• Strong organizational skills with ability to prioritize tasks and meet deadlines
• Knowledge of ethical guidelines and IRB protocols (if applicable)
• Familiarity with research/medical terminology and scientific methods
• Capable of handling administrative tasks and documentation
• Motivated, results-driven, and proactive
• Proficient in MS Office and Windows-based softwares
  
  
  

Culmen International is committed to enhancing international safety and security, strengthening homeland defense, advancing humanitarian missions, and optimizing government operations. With experience in over 150 countries, Culmen supports our clients to accomplish critical missions in challenging environments.

To learn more about Culmen International, please visit www.culmen.com.

At Culmen International, we are committed to creating and sustaining a workplace that upholds the principles of Equal Employment Opportunity (EEO). We believe in the importance of fair treatment and equal access to opportunities for all employees and applicants. Our commitment to these principles is unwavering across all our operations worldwide.