Johnson Johnson is currently seeking a Senior Site Manager - Clinical Research to join us located in Warsaw / Poland.

About Johnson Johnson

At Johnson Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com/. 

Description:

A Senior Clinical Research Associate (Senior Site Manager) serves as the primary contact point between the Sponsor and the Investigational Site. ASenior Clinical Research Associateis assigned to trial sites to ensure inspection readiness through compliance with the clinical trial protocol, company Standard Operating Procedures (SOP), Good Clinical Practice (GCP), and applicable regulations and guidelines from study start-up through to site closure. Responsibilities may include assisting with site selection, pre-trial assessment, subject recruitment and retention planning, site initiation, on-site and remote monitoring and close-out activities.Senior Clinical Research Associatewill partner with the Local Trial Manager (LTM), Clinical Trial Assistant (CTA) and Clinical Trial Manager (CTM) to ensure overall site management while performing trial related activities for assigned protocols. ASenior Clinical Research Associatemay contribute to process improvement, training and mentoring of other Site Managers.

Principal Responsibilities:

1. Acts as primary local company contact for assigned sites for specific trials.
2. May participate in site feasibility and/or pre-trial site assessment visits
3. Attends/participates in investigator meetings as needed.
4. Responsible for executing activities within site initiation and start-up, preparation and conduct of sitemonitoring (including remote monitoring), site management (by study specific systems and otherreports/dashboards) and site/study close-out according to SOPs, Work Instructions (WIs) and policies.Responsible for the implementation of analytical risk based monitoring model at the site level and towork with site to ensure timely resolution of issues found during monitoring visits.
5. Ensures site staff are trained and the corresponding training records are complete and accurate at anytime point during all trial phases. Responsible in close collaboration with LTM and central study teamfor the activities during site activation phase in order to speed up the process and activate the site inshortest possible timeframe.
6. Contributes to site level recruitment strategy and contingency planning and implementation inpartnership with other functional areas.
7. Ensures site study supplies (such as Non-Investigational Product (IP), lab kits, etc.) are adequate for trialconduct.
8. Ensures that clinical drug supplies are appropriately used, handled and stored and returns areaccurately inventoried and documented.
9. Arranges for the appropriate destruction of clinical supplies.
10. Ensures site staff complete data entry and resolve queries within expected timelines.
11. Ensures accuracy, validity and completeness of data collected at trial sites.
12. Ensures that all Adverse Events (AE) /Serious Adverse Events (SAEs )/Product Quality Complaints (PQCs)are reported within the required reporting timelines and documented as appropriate. For AEs/SAEs,ensures that they are consistent with all data collected and with the information in the sourcedocuments.
13. Maintains complete, accurate and timely data and essential documents in relevant systems utilized fortrial management.
14. Fully documents trial related activities, in particular monitoring. Writes visit reports and follow-up letter
in accordance with the SOPs. Promptly communicates relevant status information and issues to
appropriate stakeholders.
15. Reviews study files for completeness and ensures archiving retention requirements are met, including
storage in a secure area at all times.
16. Collaborates with LTM for documenting and communicating site/study progress and issues to trial
central team.
17. Attends regularly scheduled team meetings and trainings.
18. Complies with relevant training requirements. Act as local expert in assigned protocols. Develops
therapeutic knowledge sufficient to support role and responsibilities.
19. Works closely with LTM to ensure Corrective Action Preventative Action (CAPA) is completed for Quality
Assurance (QA) site audits and for quality issues identified at the site during routine monitoring and
other visit types, e.g. On Site Quality Monitoring Visit (OSQMV).
20. Prepares trial sites for close out, conduct final close out visit.
21. Tracks costs at site level and ensure payments are made, if applicable.
22. Establishes and maintains good working relationships with internal and external stakeholders in
particular investigators, trial coordinators and other site staff.
23. May participate in the Health Authority (HA) and IEC/IRB submission and notification processes as
required/appropriate.
24. Acts as a point of contact in site management practices.
25. May be assigned as a coach and mentor to a less experienced site manager.
26. May contribute to process improvement and training.
27. Leads and/or participates in special initiatives as assigned.
28. May assume additional responsibilities or special initiatives such as “Champion” or Subject Matter
Expert”.

Johnson Johnson is currently seeking a Senior Site Manager - Clinical Research to join us located in Warsaw / Poland.

About Johnson Johnson

At Johnson Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com/. 

Description:

A Senior Clinical Research Associate (Senior Site Manager) serves as the primary contact point between the Sponsor and the Investigational Site. ASenior Clinical Research Associateis assigned to trial sites to ensure inspection readiness through compliance with the clinical trial protocol, company Standard Operating Procedures (SOP), Good Clinical Practice (GCP), and applicable regulations and guidelines from study start-up through to site closure. Responsibilities may include assisting with site selection, pre-trial assessment, subject recruitment and retention planning, site initiation, on-site and remote monitoring and close-out activities.Senior Clinical Research Associatewill partner with the Local Trial Manager (LTM), Clinical Trial Assistant (CTA) and Clinical Trial Manager (CTM) to ensure overall site management while performing trial related activities for assigned protocols. ASenior Clinical Research Associatemay contribute to process improvement, training and mentoring of other Site Managers.

Principal Responsibilities:

1. Acts as primary local company contact for assigned sites for specific trials.
2. May participate in site feasibility and/or pre-trial site assessment visits
3. Attends/participates in investigator meetings as needed.
4. Responsible for executing activities within site initiation and start-up, preparation and conduct of sitemonitoring (including remote monitoring), site management (by study specific systems and otherreports/dashboards) and site/study close-out according to SOPs, Work Instructions (WIs) and policies.Responsible for the implementation of analytical risk based monitoring model at the site level and towork with site to ensure timely resolution of issues found during monitoring visits.
5. Ensures site staff are trained and the corresponding training records are complete and accurate at anytime point during all trial phases. Responsible in close collaboration with LTM and central study teamfor the activities during site activation phase in order to speed up the process and activate the site inshortest possible timeframe.
6. Contributes to site level recruitment strategy and contingency planning and implementation inpartnership with other functional areas.
7. Ensures site study supplies (such as Non-Investigational Product (IP), lab kits, etc.) are adequate for trialconduct.
8. Ensures that clinical drug supplies are appropriately used, handled and stored and returns areaccurately inventoried and documented.
9. Arranges for the appropriate destruction of clinical supplies.
10. Ensures site staff complete data entry and resolve queries within expected timelines.
11. Ensures accuracy, validity and completeness of data collected at trial sites.
12. Ensures that all Adverse Events (AE) /Serious Adverse Events (SAEs )/Product Quality Complaints (PQCs)are reported within the required reporting timelines and documented as appropriate. For AEs/SAEs,ensures that they are consistent with all data collected and with the information in the sourcedocuments.
13. Maintains complete, accurate and timely data and essential documents in relevant systems utilized fortrial management.
14. Fully documents trial related activities, in particular monitoring. Writes visit reports and follow-up letter
in accordance with the SOPs. Promptly communicates relevant status information and issues to
appropriate stakeholders.
15. Reviews study files for completeness and ensures archiving retention requirements are met, including
storage in a secure area at all times.
16. Collaborates with LTM for documenting and communicating site/study progress and issues to trial
central team.
17. Attends regularly scheduled team meetings and trainings.
18. Complies with relevant training requirements. Act as local expert in assigned protocols. Develops
therapeutic knowledge sufficient to support role and responsibilities.
19. Works closely with LTM to ensure Corrective Action Preventative Action (CAPA) is completed for Quality
Assurance (QA) site audits and for quality issues identified at the site during routine monitoring and
other visit types, e.g. On Site Quality Monitoring Visit (OSQMV).
20. Prepares trial sites for close out, conduct final close out visit.
21. Tracks costs at site level and ensure payments are made, if applicable.
22. Establishes and maintains good working relationships with internal and external stakeholders in
particular investigators, trial coordinators and other site staff.
23. May participate in the Health Authority (HA) and IEC/IRB submission and notification processes as
required/appropriate.
24. Acts as a point of contact in site management practices.
25. May be assigned as a coach and mentor to a less experienced site manager.
26. May contribute to process improvement and training.
27. Leads and/or participates in special initiatives as assigned.
28. May assume additional responsibilities or special initiatives such as “Champion” or Subject Matter
Expert”.

Education and Experience Requirements:

A minimum of a BA or BS degree in Life Sciences, Nursing or related scientific field (or equivalent experience)
is required.A minimum of 3 years of clinical trial monitoring experience is required, however, other relevant
experiences and skills may be considered by the hiring manager when considering the candidate’s eligibility.Oncology and/or Hematology experience is a very strong assetSpecific therapeutic area experience may be required depending on the position.
Strong working knowledge of GCP, company SOPs, local laws and regulations, assigned protocols and
associated protocol specific procedures including monitoring guidelines.Strong IT skills in appropriate software and company systems. Willingness to travel with occasional overnight
stay away from home.Proficient in speaking and writing the country language and English. Good written and oral communication.Ability to work on multiple trials in parallel.
Demonstrated capability to consistently deliver clinical trials.
Demonstrated capability to effectively communicate and engage with sites and sites personnel.
Demonstrated problem solving capability.

About Johnson Johnson

At Johnson Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more athttps://www.jnj.com/.

Johnson Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.

For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visitwww.careers.jnj.com.

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

DEI Statement

For more than 130 years, diversity, equity inclusion (DEI) has been a part of our cultural fabric at Johnson Johnson and woven into how we do business every day. Rooted in Our Credo, the values of DEI fuel our pursuit to create a healthier, more equitable world. Our diverse workforce and culture of belonging accelerate innovation to solve the world’s most pressing healthcare challenges.

We know that the success of our business – and our ability to deliver meaningful solutions – depends on how well we understand and meet the diverse needs of the communities we serve. Which is why we foster a culture of inclusion and belonging where all perspectives, abilities and experiences are valued and our people can reach their potential.

At Johnson Johnson, we all belong.

Education and Experience Requirements:

A minimum of a BA or BS degree in Life Sciences, Nursing or related scientific field (or equivalent experience)
is required.A minimum of 3 years of clinical trial monitoring experience is required, however, other relevant
experiences and skills may be considered by the hiring manager when considering the candidate’s eligibility.Oncology and/or Hematology experience is a very strong assetSpecific therapeutic area experience may be required depending on the position.
Strong working knowledge of GCP, company SOPs, local laws and regulations, assigned protocols and
associated protocol specific procedures including monitoring guidelines.Strong IT skills in appropriate software and company systems. Willingness to travel with occasional overnight
stay away from home.Proficient in speaking and writing the country language and English. Good written and oral communication.Ability to work on multiple trials in parallel.
Demonstrated capability to consistently deliver clinical trials.
Demonstrated capability to effectively communicate and engage with sites and sites personnel.
Demonstrated problem solving capability.

About Johnson Johnson

At Johnson Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more athttps://www.jnj.com/.

Johnson Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.

For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visitwww.careers.jnj.com.

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

DEI Statement

For more than 130 years, diversity, equity inclusion (DEI) has been a part of our cultural fabric at Johnson Johnson and woven into how we do business every day. Rooted in Our Credo, the values of DEI fuel our pursuit to create a healthier, more equitable world. Our diverse workforce and culture of belonging accelerate innovation to solve the world’s most pressing healthcare challenges.

We know that the success of our business – and our ability to deliver meaningful solutions – depends on how well we understand and meet the diverse needs of the communities we serve. Which is why we foster a culture of inclusion and belonging where all perspectives, abilities and experiences are valued and our people can reach their potential.

At Johnson Johnson, we all belong.