Parexel International Corporation
Site Contract Leader
Parexel International Corporation, Billerica, Massachusetts, us, 01821
Home Based, US
As a Site Contract Leader with Parexel you will manage the entire Clinical Site Agreement (CSA) process for a number projects, including the development of the study specific CSA strategy with the Sponsor, preparation of the corresponding country specific CSA templates and country specific budgets and also negotiation of such CSAs and budgets with the individual sites located in his/her region/country. Further, the responsibilities include managing CSA activities and liaising with PL, COL and the Sponsor to ensure that the CSA start-up deliverables are met.
Key AccountabilitiesAct as functional Leader on projects and develop study specific CSA strategy.Support site confidential disclosure agreements (Site CDA) negotiations, as required.Agree and negotiate study specific generic and/or country CSA templates and, subject to the input provided by other internal areas, negotiate the country budgets with the Sponsor.Gather relevant study information from PL/COL.Discuss and finalize specific country CSA templates with input from Sponsor, PL and/or COL, if appropriateUpon Sponsor approval of the country specific template, store the final approved and complete country CSA template and country budget in PMED, along with the corresponding CSA approval form.Arrange translations of CSA templates to local language.Prepare and negotiate with sites the respective CSA in accordance with the CSA strategy agreed with the Sponsor, CSA turnaround timelines, CTMS tracking requirements and budget negotiation parameters.Work within the defined "fallback" / approval parameters to manage / resolve significant CSA changes requested by the siteEscalate changes that fall outside the documented "fall-back" parameters, if available, to the Sponsor, SCL line manager, or any other internal point of escalation, as appropriate and ensure that sufficient background information is supplied.Proactively keep PL/COL informed about CSA progress and any issues/challenges during the CSA negotiation.Maintain CSA negotiation status accurately tracked in CTMSCollect CSA signaturesFile fully executed CSAMaintain comprehensive language trackerEarly recognition of areas of potential problems and formulate contingency plansParticipate in client, investigator and team meetings, as required.Maintain and assure quality of work generatedPrioritize effectively and respond to urgent requests within team or sponsor leadMaintain a working knowledge of, and ensure compliance with applicable ICH-GCP Guidelines, local regulatory requirements, and PAREXEL SOPs and study specific proceduresComplete routine administrative tasks in a timely manner (e.g. Timesheets, metrics, travel expense claims)SkillsPossess strong negotiation, diplomacy, team leadership skills and excellent organizational abilityExcellent interpersonal, verbal and written communication skillsAbility to motivate both individuals and a team.Ability to successfully work in a "virtual" team environmentAbility to complete tasks in an accurate, timely manner and effectively manage multiple tasksEffective time management in order to meet daily metrics or team objectivesShows commitment to and performs consistently high quality workAbility to identify and address issues proactively in a timely mannerAbility to take initiative, work independently and delegateAccountability for all assigned tasksExcellent computer and internet skills including knowledge of MS- Office products such as Excel, WordEducationDegree in business, legal or life science or other relevant work experience in Contracting, Clinical Operations or in Legal (Paralegal).
#LI-REMOTE
As a Site Contract Leader with Parexel you will manage the entire Clinical Site Agreement (CSA) process for a number projects, including the development of the study specific CSA strategy with the Sponsor, preparation of the corresponding country specific CSA templates and country specific budgets and also negotiation of such CSAs and budgets with the individual sites located in his/her region/country. Further, the responsibilities include managing CSA activities and liaising with PL, COL and the Sponsor to ensure that the CSA start-up deliverables are met.
Key AccountabilitiesAct as functional Leader on projects and develop study specific CSA strategy.Support site confidential disclosure agreements (Site CDA) negotiations, as required.Agree and negotiate study specific generic and/or country CSA templates and, subject to the input provided by other internal areas, negotiate the country budgets with the Sponsor.Gather relevant study information from PL/COL.Discuss and finalize specific country CSA templates with input from Sponsor, PL and/or COL, if appropriateUpon Sponsor approval of the country specific template, store the final approved and complete country CSA template and country budget in PMED, along with the corresponding CSA approval form.Arrange translations of CSA templates to local language.Prepare and negotiate with sites the respective CSA in accordance with the CSA strategy agreed with the Sponsor, CSA turnaround timelines, CTMS tracking requirements and budget negotiation parameters.Work within the defined "fallback" / approval parameters to manage / resolve significant CSA changes requested by the siteEscalate changes that fall outside the documented "fall-back" parameters, if available, to the Sponsor, SCL line manager, or any other internal point of escalation, as appropriate and ensure that sufficient background information is supplied.Proactively keep PL/COL informed about CSA progress and any issues/challenges during the CSA negotiation.Maintain CSA negotiation status accurately tracked in CTMSCollect CSA signaturesFile fully executed CSAMaintain comprehensive language trackerEarly recognition of areas of potential problems and formulate contingency plansParticipate in client, investigator and team meetings, as required.Maintain and assure quality of work generatedPrioritize effectively and respond to urgent requests within team or sponsor leadMaintain a working knowledge of, and ensure compliance with applicable ICH-GCP Guidelines, local regulatory requirements, and PAREXEL SOPs and study specific proceduresComplete routine administrative tasks in a timely manner (e.g. Timesheets, metrics, travel expense claims)SkillsPossess strong negotiation, diplomacy, team leadership skills and excellent organizational abilityExcellent interpersonal, verbal and written communication skillsAbility to motivate both individuals and a team.Ability to successfully work in a "virtual" team environmentAbility to complete tasks in an accurate, timely manner and effectively manage multiple tasksEffective time management in order to meet daily metrics or team objectivesShows commitment to and performs consistently high quality workAbility to identify and address issues proactively in a timely mannerAbility to take initiative, work independently and delegateAccountability for all assigned tasksExcellent computer and internet skills including knowledge of MS- Office products such as Excel, WordEducationDegree in business, legal or life science or other relevant work experience in Contracting, Clinical Operations or in Legal (Paralegal).
#LI-REMOTE