Medical Officer
GAP Solutions, Inc. · Bethesda, MD · 1 mo ago
On-siteHealthcareFull-time
We need to output HTML fragment with sections for headings like About the role, Responsibilities, Requirements, Qualifications, Skills, Benefits, Pay, Schedule. Use for each heading. Use
for each heading. Use - for any list of duties/requirements/benefits, and
for prose. Do NOT repeat job title as heading. Do NOT put Job ID etc. Remove boilerplate. Preserve all substantive info. Include a section only when posting has real specific content for it. Avoid filler like "commensurate with experience". We need to parse the posting.
The posting: "Position Objective: The Medical Officer will provide support services to satisfy the overall operational objectives of the National Human Genome Research Institute (NHGRI) within the National Institutes of Health (NIH)." That's about the role.
Then "Duties And Responsibilities" followed by a long list of duties (many repeated). We need to extract duties as list items.
Then there is no explicit "Requirements", "Qualifications", "Skills", "Benefits", "Pay", "Schedule". The posting does not mention those. So we should not create those sections. Only include sections for which we have content: About the role (maybe from Position Objective) and Responsibilities (duties). Possibly also "Qualifications" if any? Not present. So we output two sections: About the role and Responsibilities.
We need to format:
About the role
then ...
. Then Responsibilities
then - each duty.
We must preserve all substantive information, not invent or summarize away detail. So we need to include all duties listed, but we can combine duplicates? The instruction: "Preserve ALL substantive information; do NOT invent or summarize away detail." Removing duplicates might be considered summarizing away detail? It might be okay to deduplicate identical lines? The posting has many repeated sentences. Might be considered boilerplate duplication. The instruction also says: "Remove cookie/navigation/legal/EEO/equal-opportunity/scam-warning boilerplate, duplicated lines, and application instructions." So we can remove duplicated lines. So we should deduplicate duties.
We need to extract unique duty statements.
Let's parse the duties text:
"Duties And Responsibilities Coordinates all aspects of clinical protocol development, review and implementation.Provide advice on the oversight of clinical trials and protocols.Monitors ongoing clinical studies and clinical trials.Administer clinical and basic research projects, including clinical trials; monitor progress and conduct of projects, including protection and safety of participants in clinical trials.Perform periodic medical data review - review laboratory values, adverse events, coding documentaries and data tables, listing and figures as needed.Provide expertise for ongoing trials, including suitability of volunteers for enrollment into a study, consult for protocol PIs, and assist in safety oversight/assessments.Evaluates existing protocols and provides suggestions for design, execution and improvement.Collaborate with staff on the review, planning and implementation of clinical trials and ensure all concerns are addressed.Plan, implement, coordinate and evaluate programs and initiatives in the assigned specialty area of research.Establish goals and objectives for the assigned research area and organize efforts to initiate pioneering programs and resolve critical issues involving accomplishment of the research.Work with staff on protocol development; provide input on study safety design; identify medical and logistical problems that may impede the study; conduct reviews of clinical protocols and all supporting documents; and provide feedback to staff and clinical investigators.Assists in developing protocols for future clinical projects.Formulate concepts to foster research in new of underdeveloped areas of research.Produces various detailed reports for use by upper clinic or laboratory management.Help collect, collate, and analyze data pertinent to genetic disorders, and according to the research aims of the MGU.Review pertinent literature to provide a scientifically rigorous review of the subject matter. 4Provide written scientific reports on specific symptom management topics as needed. 5Participate in discussions of and prepare written summaries of evaluations of clinical trial concepts.Provide oral and/or written reports and status updates of on-going projects.Analyze data from clinical trials and research investigations; prepare abstracts for submission and manuscripts for publication.Update and maintain patient and protocol records; prepare reports are required.Evaluates various reports and safety monitoring plans and produces detailed reports for use by upper clinic or laboratory management. Participate in discussions of and prepare written summaries of evaluations of clinical trial concepts.Participates in site visits as needed.Take part in site visits to review and assess medical issues.Reviews the clinical protocols for safety of the study.Provide medical expertise in protocol follow-up stages for subject safety and protection.Provides advice and guidance for all clinical trials.Review clinical trial protocols.Reviews safety reports and provides recommendations for improvement.Provide medical expertise in protocol follow-up stages for subject safety and protection.Provides guidance to staff on various clinical processes and operational issues.Provide advice on the oversight of clinical trials.Develops policies and guidelines.Formulate concepts to foster research in new of underdeveloped areas of research.Coordinates and participates in various meetings, training and safety-related educational programs.Attend and participate in scientific meetings and conferences. 2Collaborate on the planning, development, implementation and administration of research and training programs, projects, and contracts, conferences and workshops. 3Work with Medical Genomics Unit (MGU) and collaborating/aligned research and related staff to perform services that help achieve the overall goals of developing and implementing new analytic approaches and technologies to better investigate a variety of genetic conditions.Assist with IRB-related research protocol requirements relevant to MGU studies.Assist with the management of research data and use and implementation of research databases in accordance with all applicable NIH/ NHGRI, and other policies.Participate in department standing meeting, training and safety related educational programs and efforts. 1Meet with lab members to present updates Work products and documents related to contributing to ongoing research studies, including presentations (e.g., posters, lectures), manuscripts, and related materials.Work products and documents related to supporting administrative requirements for ongoing research, including submission of materials to the IRB and other regulatory and oversight entities.Work products and documents related to helping collect, collate, and analyze data pertinent to genetic disorders, and according to the research aims of the MGUCoordination of research subject activities.Work products and documents related to assisting with the formation and maintenance of collaborations with other investigators."
We need to split into sentences/phrases separated by periods. Many have no spaces after period. We'll need to parse manually.
Let's extract each distinct duty statement.
I'll go through and list them:
1. Coordinates all aspects of clinical protocol development, review and implementation.
2. Provide advice on the oversight of clinical trials and protocols.
3. Monitors ongoing clinical studies and clinical trials.
4. Administer clinical and basic research projects, including clinical trials; monitor progress and conduct of projects, including protection and safety of participants in clinical trials.
5. Perform periodic medical data review - review laboratory values, adverse events, coding documentaries and data tables, listing and figures as needed.
6. Provide expertise for ongoing trials, including suitability of volunteers for enrollment into a study, consult for protocol PIs, and assist in safety oversight/assessments.
7. Evaluates existing protocols and provides suggestions for design, execution and improvement.
8. Collaborate with staff on the review, planning and implementation of clinical trials and ensure all concerns are addressed.
9. Plan, implement, coordinate and evaluate programs and initiatives in the assigned specialty area of research.
10. Establish goals and objectives for the assigned research area and organize efforts to initiate pioneering programs and resolve critical issues involving accomplishment of the research.
11. Work with staff on protocol development; provide input on study safety design; identify medical and logistical problems that may impede the study; conduct reviews of clinical protocols and all supporting documents; and provide feedback to staff and clinical investigators.
12. Assists in developing protocols for future clinical projects.
13. Formulate concepts to foster research in new of underdeveloped areas of research.
14. Produces various detailed reports for use by upper clinic or laboratory management.
15. Help collect, collate, and analyze data pertinent to genetic disorders, and according to the research aims of the MGU.
16. Review pertinent literature to provide a scientifically rigorous review of the subject matter.
17. Provide written scientific reports on specific symptom management topics as needed.
18. Participate in discussions of and prepare written summaries of evaluations of clinical trial concepts.
19. Provide oral and/or written reports and status updates of on-going projects.
20. Analyze data from clinical trials and research investigations; prepare abstracts for submission and manuscripts for publication.
21. Update and maintain patient and protocol records; prepare reports are required.
22. Evaluates various reports and safety monitoring plans and produces detailed reports for use by upper clinic or laboratory management.
23. Participate in discussions of and prepare written summaries of evaluations of clinical trial concepts. (duplicate of 18)
24. Participates in site visits as needed.
25. Take part in site visits to review and assess medical issues.
26. Reviews the clinical protocols for safety of the study.
27. Provide medical expertise in protocol follow-up stages for subject safety and protection.
28. Provides advice and guidance for all clinical trials.
29. Review clinical trial protocols.
30. Reviews safety reports and provides recommendations for improvement.
31. Provide medical expertise in protocol follow-up stages for subject safety and protection. (duplicate of 27)
32. Provides guidance to staff on various clinical processes and operational issues.
33. Provide advice on the oversight of clinical trials. (duplicate of 2)
34. Develops policies and guidelines.
35. Formulate concepts to foster research in new of underdeveloped areas of research. (duplicate of 13)
36. Coordinates and participates in various meetings, training and safety-related educational programs.
37. Attend and participate in scientific meetings and conferences.
38. Collaborate on the planning, development, implementation and administration of research and training programs, projects, and contracts, conferences and workshops.
39. Work with Medical Genomics Unit (MGU) and collaborating/aligned research and related staff to perform services that help achieve the overall goals of developing and implementing new analytic approaches and technologies to better investigate a variety of genetic conditions.
40. Assist with IRB-related research protocol requirements relevant to MGU studies.
41. Assist with the management of research data and use and implementation of research databases in accordance with all applicable NIH/ NHGRI, and other policies.
42. Participate in department standing meeting, training and safety related educational programs and efforts.
43. Meet with lab members to present updates
44. Work products and documents related to contributing to ongoing research studies, including presentations (e.g., posters, lectures), manuscripts, and related materials.
45. Work products and documents related to supporting administrative requirements for ongoing research, including submission of materials to the IRB and other regulatory and oversight entities.
46. Work products and documents related to helping collect, collate, and analyze data pertinent to genetic disorders, and according to the research aims of the MGU
47. Coordination of research subject activities.
48. Work products and documents related to assisting with the formation and maintenance of collaborations with other investigators.
Now we need to remove duplicates. Let's identify duplicates:
- 2 and 33 both "Provide advice on the oversight of clinical trials." (same)
- 18 and 23 duplicate.
- 27 and 31 duplicate.
- 13 and 35 duplicate.
- Possibly others: "Provide medical expertise in protocol follow-up stages for subject safety and protection." appears twice (27,31). Already noted.
- "Review clinical trial protocols." appears as 29 only.
- "Reviews safety reports and provides recommendations for improvement." appears as 30 only.
- "Provides advice and guidance for all clinical trials." appears as 28 only.
- "Provides guidance to staff on various clinical processes and operational issues." appears as 32 only.
- "Develops policies and guidelines." appears as 34 only.
- "Coordinates and participates in various meetings, training and safety-related educational programs." appears as 36 only.
- "Attend and participate in scientific meetings and
for prose. Do NOT repeat job title as heading. Do NOT put Job ID etc. Remove boilerplate. Preserve all substantive info. Include a section only when posting has real specific content for it. Avoid filler like "commensurate with experience". We need to parse the posting. The posting: "Position Objective: The Medical Officer will provide support services to satisfy the overall operational objectives of the National Human Genome Research Institute (NHGRI) within the National Institutes of Health (NIH)." That's about the role. Then "Duties And Responsibilities" followed by a long list of duties (many repeated). We need to extract duties as list items. Then there is no explicit "Requirements", "Qualifications", "Skills", "Benefits", "Pay", "Schedule". The posting does not mention those. So we should not create those sections. Only include sections for which we have content: About the role (maybe from Position Objective) and Responsibilities (duties). Possibly also "Qualifications" if any? Not present. So we output two sections: About the role and Responsibilities. We need to format:
About the role
then...
. ThenResponsibilities
then- each duty. We must preserve all substantive information, not invent or summarize away detail. So we need to include all duties listed, but we can combine duplicates? The instruction: "Preserve ALL substantive information; do NOT invent or summarize away detail." Removing duplicates might be considered summarizing away detail? It might be okay to deduplicate identical lines? The posting has many repeated sentences. Might be considered boilerplate duplication. The instruction also says: "Remove cookie/navigation/legal/EEO/equal-opportunity/scam-warning boilerplate, duplicated lines, and application instructions." So we can remove duplicated lines. So we should deduplicate duties. We need to extract unique duty statements. Let's parse the duties text: "Duties And Responsibilities Coordinates all aspects of clinical protocol development, review and implementation.Provide advice on the oversight of clinical trials and protocols.Monitors ongoing clinical studies and clinical trials.Administer clinical and basic research projects, including clinical trials; monitor progress and conduct of projects, including protection and safety of participants in clinical trials.Perform periodic medical data review - review laboratory values, adverse events, coding documentaries and data tables, listing and figures as needed.Provide expertise for ongoing trials, including suitability of volunteers for enrollment into a study, consult for protocol PIs, and assist in safety oversight/assessments.Evaluates existing protocols and provides suggestions for design, execution and improvement.Collaborate with staff on the review, planning and implementation of clinical trials and ensure all concerns are addressed.Plan, implement, coordinate and evaluate programs and initiatives in the assigned specialty area of research.Establish goals and objectives for the assigned research area and organize efforts to initiate pioneering programs and resolve critical issues involving accomplishment of the research.Work with staff on protocol development; provide input on study safety design; identify medical and logistical problems that may impede the study; conduct reviews of clinical protocols and all supporting documents; and provide feedback to staff and clinical investigators.Assists in developing protocols for future clinical projects.Formulate concepts to foster research in new of underdeveloped areas of research.Produces various detailed reports for use by upper clinic or laboratory management.Help collect, collate, and analyze data pertinent to genetic disorders, and according to the research aims of the MGU.Review pertinent literature to provide a scientifically rigorous review of the subject matter. 4Provide written scientific reports on specific symptom management topics as needed. 5Participate in discussions of and prepare written summaries of evaluations of clinical trial concepts.Provide oral and/or written reports and status updates of on-going projects.Analyze data from clinical trials and research investigations; prepare abstracts for submission and manuscripts for publication.Update and maintain patient and protocol records; prepare reports are required.Evaluates various reports and safety monitoring plans and produces detailed reports for use by upper clinic or laboratory management. Participate in discussions of and prepare written summaries of evaluations of clinical trial concepts.Participates in site visits as needed.Take part in site visits to review and assess medical issues.Reviews the clinical protocols for safety of the study.Provide medical expertise in protocol follow-up stages for subject safety and protection.Provides advice and guidance for all clinical trials.Review clinical trial protocols.Reviews safety reports and provides recommendations for improvement.Provide medical expertise in protocol follow-up stages for subject safety and protection.Provides guidance to staff on various clinical processes and operational issues.Provide advice on the oversight of clinical trials.Develops policies and guidelines.Formulate concepts to foster research in new of underdeveloped areas of research.Coordinates and participates in various meetings, training and safety-related educational programs.Attend and participate in scientific meetings and conferences. 2Collaborate on the planning, development, implementation and administration of research and training programs, projects, and contracts, conferences and workshops. 3Work with Medical Genomics Unit (MGU) and collaborating/aligned research and related staff to perform services that help achieve the overall goals of developing and implementing new analytic approaches and technologies to better investigate a variety of genetic conditions.Assist with IRB-related research protocol requirements relevant to MGU studies.Assist with the management of research data and use and implementation of research databases in accordance with all applicable NIH/ NHGRI, and other policies.Participate in department standing meeting, training and safety related educational programs and efforts. 1Meet with lab members to present updates Work products and documents related to contributing to ongoing research studies, including presentations (e.g., posters, lectures), manuscripts, and related materials.Work products and documents related to supporting administrative requirements for ongoing research, including submission of materials to the IRB and other regulatory and oversight entities.Work products and documents related to helping collect, collate, and analyze data pertinent to genetic disorders, and according to the research aims of the MGUCoordination of research subject activities.Work products and documents related to assisting with the formation and maintenance of collaborations with other investigators." We need to split into sentences/phrases separated by periods. Many have no spaces after period. We'll need to parse manually. Let's extract each distinct duty statement. I'll go through and list them: 1. Coordinates all aspects of clinical protocol development, review and implementation. 2. Provide advice on the oversight of clinical trials and protocols. 3. Monitors ongoing clinical studies and clinical trials. 4. Administer clinical and basic research projects, including clinical trials; monitor progress and conduct of projects, including protection and safety of participants in clinical trials. 5. Perform periodic medical data review - review laboratory values, adverse events, coding documentaries and data tables, listing and figures as needed. 6. Provide expertise for ongoing trials, including suitability of volunteers for enrollment into a study, consult for protocol PIs, and assist in safety oversight/assessments. 7. Evaluates existing protocols and provides suggestions for design, execution and improvement. 8. Collaborate with staff on the review, planning and implementation of clinical trials and ensure all concerns are addressed. 9. Plan, implement, coordinate and evaluate programs and initiatives in the assigned specialty area of research. 10. Establish goals and objectives for the assigned research area and organize efforts to initiate pioneering programs and resolve critical issues involving accomplishment of the research. 11. Work with staff on protocol development; provide input on study safety design; identify medical and logistical problems that may impede the study; conduct reviews of clinical protocols and all supporting documents; and provide feedback to staff and clinical investigators. 12. Assists in developing protocols for future clinical projects. 13. Formulate concepts to foster research in new of underdeveloped areas of research. 14. Produces various detailed reports for use by upper clinic or laboratory management. 15. Help collect, collate, and analyze data pertinent to genetic disorders, and according to the research aims of the MGU. 16. Review pertinent literature to provide a scientifically rigorous review of the subject matter. 17. Provide written scientific reports on specific symptom management topics as needed. 18. Participate in discussions of and prepare written summaries of evaluations of clinical trial concepts. 19. Provide oral and/or written reports and status updates of on-going projects. 20. Analyze data from clinical trials and research investigations; prepare abstracts for submission and manuscripts for publication. 21. Update and maintain patient and protocol records; prepare reports are required. 22. Evaluates various reports and safety monitoring plans and produces detailed reports for use by upper clinic or laboratory management. 23. Participate in discussions of and prepare written summaries of evaluations of clinical trial concepts. (duplicate of 18) 24. Participates in site visits as needed. 25. Take part in site visits to review and assess medical issues. 26. Reviews the clinical protocols for safety of the study. 27. Provide medical expertise in protocol follow-up stages for subject safety and protection. 28. Provides advice and guidance for all clinical trials. 29. Review clinical trial protocols. 30. Reviews safety reports and provides recommendations for improvement. 31. Provide medical expertise in protocol follow-up stages for subject safety and protection. (duplicate of 27) 32. Provides guidance to staff on various clinical processes and operational issues. 33. Provide advice on the oversight of clinical trials. (duplicate of 2) 34. Develops policies and guidelines. 35. Formulate concepts to foster research in new of underdeveloped areas of research. (duplicate of 13) 36. Coordinates and participates in various meetings, training and safety-related educational programs. 37. Attend and participate in scientific meetings and conferences. 38. Collaborate on the planning, development, implementation and administration of research and training programs, projects, and contracts, conferences and workshops. 39. Work with Medical Genomics Unit (MGU) and collaborating/aligned research and related staff to perform services that help achieve the overall goals of developing and implementing new analytic approaches and technologies to better investigate a variety of genetic conditions. 40. Assist with IRB-related research protocol requirements relevant to MGU studies. 41. Assist with the management of research data and use and implementation of research databases in accordance with all applicable NIH/ NHGRI, and other policies. 42. Participate in department standing meeting, training and safety related educational programs and efforts. 43. Meet with lab members to present updates 44. Work products and documents related to contributing to ongoing research studies, including presentations (e.g., posters, lectures), manuscripts, and related materials. 45. Work products and documents related to supporting administrative requirements for ongoing research, including submission of materials to the IRB and other regulatory and oversight entities. 46. Work products and documents related to helping collect, collate, and analyze data pertinent to genetic disorders, and according to the research aims of the MGU 47. Coordination of research subject activities. 48. Work products and documents related to assisting with the formation and maintenance of collaborations with other investigators. Now we need to remove duplicates. Let's identify duplicates: - 2 and 33 both "Provide advice on the oversight of clinical trials." (same) - 18 and 23 duplicate. - 27 and 31 duplicate. - 13 and 35 duplicate. - Possibly others: "Provide medical expertise in protocol follow-up stages for subject safety and protection." appears twice (27,31). Already noted. - "Review clinical trial protocols." appears as 29 only. - "Reviews safety reports and provides recommendations for improvement." appears as 30 only. - "Provides advice and guidance for all clinical trials." appears as 28 only. - "Provides guidance to staff on various clinical processes and operational issues." appears as 32 only. - "Develops policies and guidelines." appears as 34 only. - "Coordinates and participates in various meetings, training and safety-related educational programs." appears as 36 only. - "Attend and participate in scientific meetings and