Research Assistant- Surveys
CORPORATE
Manhasset, NYFull-time
Behavioral Health Market Context
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Job Description
ude:
1. Planning/Reporting
• Collaborates with investigator and other team members in developing plans, organization, implementation and monitoring for research projects, interpretation of results, and preparation of manuscripts or reports.
• Sets-up related interviews, as appropriate.
• Participates in compilation/writing of integrated reports and preparation of presentations and manuscripts of scientific meetings and technical journals.
2. Protocols/Procedures/Techniques
• Organizes and conducts assigned studies, independently, following and adhering to current experimental protocols. Initial set-up and/or results may be reviewed.
• Learns, researches and recommends new experimental procedures, as necessary
• Develops forms and questionnaires and coordinates the application of research techniques, as necessary.
• Ensures work is in compliance with the currently approved protocols, with Good Clinical Research Practice (GCP), and with applicable regulatory requirement(s).
• Participates in design and writing of protocols, case report forms and informed consent forms for clinical trials.
3. Data
• Performs a variety of independent activities involved in the collection, verification, analysis, documentation and interpretation of research data.
• Selects sources of information and specific data.
• Prepares correspondence to locate the specific data, as required.
• Evaluates and interprets collected data, and prepares presentations, reports and analyses describing progress, trends, and recommendations or conclusions.
4. Performs related duties, as required.
Qualifications
• Bachelor's Degree, required.
• Research or analytical experience, preferred
• Maintains current knowledge of research study area including attending scientific/professional meetings and training courses as appropriate.
• Works effectively as part of a team with good interpersonal skills.
• Able to take initiative and work interdependently, meet deadlines with a sense of urgency, multitask, adjust to shifting priorities, communicate effectively, and work under defined rules and regulations.
• Detail-oriented. Uses good judgment. Possesses perseverance and persistence.
About the Company:
CORPORATE
1. Planning/Reporting
• Collaborates with investigator and other team members in developing plans, organization, implementation and monitoring for research projects, interpretation of results, and preparation of manuscripts or reports.
• Sets-up related interviews, as appropriate.
• Participates in compilation/writing of integrated reports and preparation of presentations and manuscripts of scientific meetings and technical journals.
2. Protocols/Procedures/Techniques
• Organizes and conducts assigned studies, independently, following and adhering to current experimental protocols. Initial set-up and/or results may be reviewed.
• Learns, researches and recommends new experimental procedures, as necessary
• Develops forms and questionnaires and coordinates the application of research techniques, as necessary.
• Ensures work is in compliance with the currently approved protocols, with Good Clinical Research Practice (GCP), and with applicable regulatory requirement(s).
• Participates in design and writing of protocols, case report forms and informed consent forms for clinical trials.
3. Data
• Performs a variety of independent activities involved in the collection, verification, analysis, documentation and interpretation of research data.
• Selects sources of information and specific data.
• Prepares correspondence to locate the specific data, as required.
• Evaluates and interprets collected data, and prepares presentations, reports and analyses describing progress, trends, and recommendations or conclusions.
4. Performs related duties, as required.
Qualifications
• Bachelor's Degree, required.
• Research or analytical experience, preferred
• Maintains current knowledge of research study area including attending scientific/professional meetings and training courses as appropriate.
• Works effectively as part of a team with good interpersonal skills.
• Able to take initiative and work interdependently, meet deadlines with a sense of urgency, multitask, adjust to shifting priorities, communicate effectively, and work under defined rules and regulations.
• Detail-oriented. Uses good judgment. Possesses perseverance and persistence.
About the Company:
CORPORATE
Qualifications
- •Bachelor's Degree, required
- •Maintains current knowledge of research study area including attending scientific/professional meetings and training courses as appropriate
- •Works effectively as part of a team with good interpersonal skills
- •Able to take initiative and work interdependently, meet deadlines with a sense of urgency, multitask, adjust to shifting priorities, communicate effectively, and work under defined rules and regulations
- •Detail-oriented
- •Possesses perseverance and persistence
Benefits
Responsibilities
- •Performs a variety of independent activities involved in planning, organizing and conducting assigned portion(s) of research studies
- •Participates in the coordination of sharing information, lending assistance, and solving problems with other team members, as needed
- •Assignments may be fewer and less complex and may receive general guidance and/or direction
- •Planning/Reporting
- •Collaborates with investigator and other team members in developing plans, organization, implementation and monitoring for research projects, interpretation of results, and preparation of manuscripts or reports
- •Sets-up related interviews, as appropriate
- •Participates in compilation/writing of integrated reports and preparation of presentations and manuscripts of scientific meetings and technical journals
- •Protocols/Procedures/Techniques
- •Organizes and conducts assigned studies, independently, following and adhering to current experimental protocols
- •Initial set-up and/or results may be reviewed
- •Learns, researches and recommends new experimental procedures, as necessary
- •Develops forms and questionnaires and coordinates the application of research techniques, as necessary
- •Ensures work is in compliance with the currently approved protocols, with Good Clinical Research Practice (GCP), and with applicable regulatory requirement(s)
- •Participates in design and writing of protocols, case report forms and informed consent forms for clinical trials
- •Performs a variety of independent activities involved in the collection, verification, analysis, documentation and interpretation of research data
- •Selects sources of information and specific data
- •Prepares correspondence to locate the specific data, as required
- •Evaluates and interprets collected data, and prepares presentations, reports and analyses describing progress, trends, and recommendations or conclusions
- •Performs related duties, as required
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