Prepare, negotiate, and finalize clinical trial agreements and ancillary agreements for company sponsored and/or investigator-initiated studies through direct negotiation with clinical trial sites or via oversite of a Clinical Research Organization responsible for contract negotiations.• Responsible for analyzing requirements and translating into appropriate contracts and budgets for clinical trial agreements and other relevant legal documents. Responsible for reviewing all… Show more Prepare, negotiate, and finalize clinical trial agreements and ancillary agreements for company sponsored and/or investigator-initiated studies through direct negotiation with clinical trial sites or via oversite of a Clinical Research Organization responsible for contract negotiations.• Responsible for analyzing requirements and translating into appropriate contracts and budgets for clinical trial agreements and other relevant legal documents. Responsible for reviewing all study specific tracking requirements for accuracy and completeness as well as delivering against contracting cycle time targets. • Work with global teams to review and analyze contractual terms and conditions. Assess legal and budget risks in conjunction with team support functions. Partner with Healthcare Compliance, Risk Management, Privacy and other stakeholders to obtain guidance and drive resolution. Analyze investigator fees in relation to fair market value pricing and ensure alignment with regional standards and the J&J pricing guidelines. Participate in and/or lead approval escalations as appropriate. • Provide specialized support and guidance on negotiations in confidentiality agreements, informed consent forms and other ancillary contract documents, as required. Determine potential needs for contract amendments and manage amendment lifecycle. Ensure that contractual terms and provisions are in compliance with corporate process, systems, and strategies• Provide project management oversight to CROs contracted to negotiate CTAs globally, inclusive of training and supervision to ensure adherence to timelines/targets.• Onboard and train new staff and meet regularly with team members to ensure studies are properly supported and identify contracting issues and potential solutions. Assist in resolution of site/study related concerns. Mentor and guide teams on processes and procedures. Serve as a key liaison with management on staff performance and development. Show less

Prepare, negotiate and finalize agreements and budgets related to clinical trials and/or overseeing a Clinical Research Organization responsible for contract negotiations. Responsibilities: • 1.Services rendered will adhere to applicable Johnson & Johnson SOPs, WIs, policies, local regulatory requirements, etc. • 2.Prepare, negotiate, and finalize clinical trial agreements and ancillary agreements for company sponsored and/or investigator-initiated studies through direct negotiation… Show more Prepare, negotiate and finalize agreements and budgets related to clinical trials and/or overseeing a Clinical Research Organization responsible for contract negotiations. Responsibilities: • 1.Services rendered will adhere to applicable Johnson & Johnson SOPs, WIs, policies, local regulatory requirements, etc. • 2.Prepare, negotiate, and finalize clinical trial agreements and ancillary agreements for company sponsored and/or investigator-initiated studies through direct negotiation with clinical trial sites or via oversite of a Clinical Research Organization responsible for contract negotiations. Responsible for delivery on established targets/measurements. • 3.Work with global teams to review and analyze contractual terms and conditions. Assess legal and budget risks in conjunction with team support functions. Partner with Health care Compliance, Risk Management, Privacy and other stakeholders to obtain guidance and drive resolution. Escalate as appropriate. • 4.Analyze investigator fees in relation to fair market value pricing and ensure alignment with regional standards and the J&J pricing guidelines. Participate in and/or lead approval escalations as appropriate. • 5.Provide support for negotiations in confidentiality agreements, informed consent forms and other ancillary contract documents as required. • Participate in discussions related to the development of site/investigator budgets aligned with fair market value. • Manage the contract amendment life cycle. • 6.Work with the global CCS team as necessary to review and analyze contractual terms to reach resolution. Assess risks of budget and legal provisions in conjunction with members of the CCS team and support functions. Escalate issues as appropriate. • 7.Work proactively to provide recommendations to improve processes and establish refinements that reduce cycle time, create savings and improve efficiency in the initiation of clinical trial sites. Show less

• 1.Play service manager role in HP supplier management department through DLM/HP Flex team to oversight APAC maintenance issues of related products and equipment. • 2.Join weekly regular calls with authorized monitor repairs and original design manufacturers to review and monitor their dashboard performance • 3.Negotiate the price and other contract terms with all HP’s APAC suppliers. Ensure the contracts will be successfully implemented and handling the emergency issues • 4.Review… Show more • 1.Play service manager role in HP supplier management department through DLM/HP Flex team to oversight APAC maintenance issues of related products and equipment. • 2.Join weekly regular calls with authorized monitor repairs and original design manufacturers to review and monitor their dashboard performance • 3.Negotiate the price and other contract terms with all HP’s APAC suppliers. Ensure the contracts will be successfully implemented and handling the emergency issues • 4.Review the inventory plans made by AMRs and ODMs to make sure the safety inventory level • 5.Validate the charge back from all AMRs to check all costs are matched with weekly the reports they provided • 6.Perform root cause analysis and corrective actions& preventive actions reviewing and make sure the effectiveness checking if any error or issue occurs. Show less

• 1.Work as senior contract specialist role in the China local CRO to support the clinical trial site contracting pieces. • 2.Participant sponsors’ contracting and pricing training and follow the provided guidance to perform site contracting. • 3.Follow sponsor fallback documents to perform clinical trial contract budget reviewing and language reviewing and need ensure compliance with applicable ICH-GCP and meet site related policy. • 4.Use sponsor pricing documents, tools, such as… Show more • 1.Work as senior contract specialist role in the China local CRO to support the clinical trial site contracting pieces. • 2.Participant sponsors’ contracting and pricing training and follow the provided guidance to perform site contracting. • 3.Follow sponsor fallback documents to perform clinical trial contract budget reviewing and language reviewing and need ensure compliance with applicable ICH-GCP and meet site related policy. • 4.Use sponsor pricing documents, tools, such as Fair Market Value benchmark files for site negotiation. • 5.Track cycle time from gathering country intelligence to CTA fully executed. • 6. Communicate with internal study start up team and address RA submission, EC/IRB approval timeline to ensure site GCP office reviewer can start CTA reviewing and the CTA finalization can achieve based on the goal Show less

• 1.Perform basic data entry work for business contracts and keep contract templates version updating in Health Care and Cosmetics outsourced domains. • 2.Prepare and support the response for information or proposal, track open actions and completed related tasks to follow business engagement team to ensure draft files submission is on time. • 3.Connect with internal stakeholders to address on any progress for bidding documents and proposal creation, amendment, finalization •… Show more • 1.Perform basic data entry work for business contracts and keep contract templates version updating in Health Care and Cosmetics outsourced domains. • 2.Prepare and support the response for information or proposal, track open actions and completed related tasks to follow business engagement team to ensure draft files submission is on time. • 3.Connect with internal stakeholders to address on any progress for bidding documents and proposal creation, amendment, finalization • 4.Ensure data entry and translation accuracy, work proactively to improve processes, and establish refinements that reduce average handling time • 5.Assist team leader to conduct trace and perform root cause analysis based on any mistakes or findings. • 6.Ensure appropriate daily contact with customers and take orders from global customers Show less

- Participating in different surveys (Creating the questionnaires, data input and analysis)- Book editing and assessment grading- Taking care of bookkeeping, filling, marketing