What are the responsibilities and job description for the Study Start Up Leader (Clinical Trials) - Home-based position at Parexel - USA?
Job Description
Parexel has new opportunities for home based Study Start UP Leaders to join our global start up team. ,
The Associate Study Start-up Leader/ Study Start-Up Leader is accountable for the execution of the study start-up strategy and planning, including the management and coordination of start-up activities such as alignment to country regulations, Core/Site document collection/ approval, ICF customization/approval, EC and RA/ MoH submissions, SIV scheduling and activation requirements.
The Senior Study Start-Up Leader, is accountable as noted above including:
• Acting as study-level program lead, such as managing multiple protocol delivery for a Sponsor or asset development.
• Acting as an Enterprise or Biotech level lead and provide expert level knowledge on agreed partnership process.
• Additional responsibilities may include:
o Study Start-Up Leader mentorship
o Participation in training and support programs
o Fulfilling subject matter expert or process improvement roles within Clinical Operations.
Key Accountabilities:
• Manage the study start up process, through development of a site activation strategy and to oversee start-up delivery and governance.
• Coordinate, develop and articulate the critical path planning, and implement as part of the Site Initiation Scheduling, System Set-up, EDL Management, EC & RA/ MoH Strategy, ICF Customization, Risk Mitigations, Monitoring Plan, Site Activation Requirements & Relevant Tools.
• Collaborate and communicate within the Global study team matrix to provide study start up strategy, input to milestone development, and alignment of operational targets to ensure timely delivery of study start up activities.
• Participate in client meetings with respect to study start up, including endorsement of the SSU Operational Targets & mitigation of delivery risks, establishing client expectations for delivery, communication, reporting, and metrics.
• Partner closely with both Functional Leaders and Local Site Managers to proactively identify study start up related issues
• Develop and execute corrective actions to mitigate risks to activation timelines
• Ensure that relevant - systems are maintained and up to date to analyze study start-up progress metrics against targets/timelines (at a project/country/site level).
• Deliver and maintain client-focused reporting to measure performance and proactively identify issues for resolution
Qualifications
• Knowledge of applicable international regulatory requirements and guidelines (i.e. ICH-GCP, and/ or EU-Directives).
• Critical thinking and problem solving
• Strategic & tactical thinking skills
• Conflict management skills
• Consulting skills
• Strategic and creative risk management and contingency planning
• Ability to lead virtual teams across cultures and locations
• Excellent interpersonal, verbal, written and presentation skills
• Client-focused action-oriented approach to work
• Strong Leadership skills, with ability to influence both vertically and horizontally
• Ability to manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail
• Able to work independently and manage assignments from a distance
• Sense of urgency and organization in completing tasks
• Strong understanding of cultural differences
• Willingness to work in a matrix environment and to value the importance of teamwork.
• Proficient computer and internet skills, including working knowledge of MS-office applications, such as MS Outlook, Word and Excel
• Ability to travel, as required
This role may be subject to government and/or customer requirements regarding vaccination against COVID-19 that are more stringent than Parexel policy. Accordingly, successful applicants may need to be either vaccinated against COVID-19 or have an approved religious or medical exemption. Employment is contingent on disclosure of your COVID-19 vaccination status and, if relevant, proof of vaccination.
Why Work at Parexel
There are pivotal moments in every career: Sharing new treatments. Improving processes. Delivering life-saving advances. The people who succeed are the ones who make the journey go further and faster every time. What if you had a partner to support you as you reach the next level in your professional path? A partner who believes a collaborative environment is key to achieving your goals? A partner who is dedicated to your health and wellness so you can help make a difference in the lives of millions worldwide?
That’s Parexel. We’re a diverse team of professionals focused on one goal: getting treatments into the hands of those who need them most. Working together, the results we bring to our clients and the opportunities we bring to our team get better with every step.
How can we help you on your journey? Find your path, and learn more on LinkedIn , YouTube , Facebook , Twitter , and Glassdoor .
Parexel has new opportunities for home based Study Start UP Leaders to join our global start up team. ,
The Associate Study Start-up Leader/ Study Start-Up Leader is accountable for the execution of the study start-up strategy and planning, including the management and coordination of start-up activities such as alignment to country regulations, Core/Site document collection/ approval, ICF customization/approval, EC and RA/ MoH submissions, SIV scheduling and activation requirements.
The Senior Study Start-Up Leader, is accountable as noted above including:
• Acting as study-level program lead, such as managing multiple protocol delivery for a Sponsor or asset development.
• Acting as an Enterprise or Biotech level lead and provide expert level knowledge on agreed partnership process.
• Additional responsibilities may include:
o Study Start-Up Leader mentorship
o Participation in training and support programs
o Fulfilling subject matter expert or process improvement roles within Clinical Operations.
Key Accountabilities:
• Manage the study start up process, through development of a site activation strategy and to oversee start-up delivery and governance.
• Coordinate, develop and articulate the critical path planning, and implement as part of the Site Initiation Scheduling, System Set-up, EDL Management, EC & RA/ MoH Strategy, ICF Customization, Risk Mitigations, Monitoring Plan, Site Activation Requirements & Relevant Tools.
• Collaborate and communicate within the Global study team matrix to provide study start up strategy, input to milestone development, and alignment of operational targets to ensure timely delivery of study start up activities.
• Participate in client meetings with respect to study start up, including endorsement of the SSU Operational Targets & mitigation of delivery risks, establishing client expectations for delivery, communication, reporting, and metrics.
• Partner closely with both Functional Leaders and Local Site Managers to proactively identify study start up related issues
• Develop and execute corrective actions to mitigate risks to activation timelines
• Ensure that relevant - systems are maintained and up to date to analyze study start-up progress metrics against targets/timelines (at a project/country/site level).
• Deliver and maintain client-focused reporting to measure performance and proactively identify issues for resolution
Qualifications
• Knowledge of applicable international regulatory requirements and guidelines (i.e. ICH-GCP, and/ or EU-Directives).
• Critical thinking and problem solving
• Strategic & tactical thinking skills
• Conflict management skills
• Consulting skills
• Strategic and creative risk management and contingency planning
• Ability to lead virtual teams across cultures and locations
• Excellent interpersonal, verbal, written and presentation skills
• Client-focused action-oriented approach to work
• Strong Leadership skills, with ability to influence both vertically and horizontally
• Ability to manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail
• Able to work independently and manage assignments from a distance
• Sense of urgency and organization in completing tasks
• Strong understanding of cultural differences
• Willingness to work in a matrix environment and to value the importance of teamwork.
• Proficient computer and internet skills, including working knowledge of MS-office applications, such as MS Outlook, Word and Excel
• Ability to travel, as required
This role may be subject to government and/or customer requirements regarding vaccination against COVID-19 that are more stringent than Parexel policy. Accordingly, successful applicants may need to be either vaccinated against COVID-19 or have an approved religious or medical exemption. Employment is contingent on disclosure of your COVID-19 vaccination status and, if relevant, proof of vaccination.
Why Work at Parexel
There are pivotal moments in every career: Sharing new treatments. Improving processes. Delivering life-saving advances. The people who succeed are the ones who make the journey go further and faster every time. What if you had a partner to support you as you reach the next level in your professional path? A partner who believes a collaborative environment is key to achieving your goals? A partner who is dedicated to your health and wellness so you can help make a difference in the lives of millions worldwide?
That’s Parexel. We’re a diverse team of professionals focused on one goal: getting treatments into the hands of those who need them most. Working together, the results we bring to our clients and the opportunities we bring to our team get better with every step.
How can we help you on your journey? Find your path, and learn more on LinkedIn , YouTube , Facebook , Twitter , and Glassdoor .
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