2 Site Activation Specialist jobs in the Philippines
Site Activation Specialist
Pasig, Palawan
IQVIA
Posted 11 days ago
Job Viewed
Job Description
**Job Responsibilities:**
+ Serve as Single Point of Contact (SPOC) in assigned studies for investigative sites, RSU Team Lead, Clinical Operations, Feasibility, Site Identification, Project Leadership and GICS. Ensure adherence to standard operating procedures (SOPs), work instructions (WIs), quality of designated deliverables and to project timelines. Where applicable, act as a Country Lead for projects with no regional Lead assigned.
+ Perform Regulatory, Start-up and Maintenance activities according to applicable regulations, SOPs and work instructions.
+ Prepare site regulatory documents, reviewing for completeness and accuracy.
+ Review, prepare and negotiate site contracts and budgets with sites, if applicable.
+ Ensure accurate completion and maintenance of internal systems, databases and tracking tools with project specific information.
+ Ensure contracts are fully executed, regulatory documents and approvals are granted, IP Release authorized and specific project deliverables are completed.
+ Review and provide feedback to management on site performance metrics.
+ Review, establish and agree on project planning and project timelines. Ensure overall project efficiency and adherence to project timelines. Ensure monitoring measures are in place and implement contingency plan as needed.
+ May contribute to the collection, interpretation, analysis and dissemination of accurate regulatory intelligence to support assigned studies and wider company, as required.
+ May assist in pre-award activities including bid defenses, proposals and oversights of the scope of work at country level.
+ May provide input into contract and budget template development.
+ May support importation activities.
+ May have direct contact with sponsors on specific initiatives.
+ May act as Local Regulatory, Ethics and Contract Expert and reviewer of ICF.
+ May act as mentor, and prepare and deliver country-specific training, for less experienced staff.
+ May participate in feasibility and/or site identification activities.
+ May perform Site Selection Visits if a trained monitor.
**Job Requirements:**
+ Bachelor's Degree in life sciences or a related field and 3 years' clinical research or other relevant experience; or equivalent combination of education, training and experience.
+ In-depth knowledge of clinical systems, procedures, and corporate standards.
+ Good negotiating and communication skills with ability to challenge, if applicable.
+ Effective communication, organizational, and interpersonal skills.
+ Ability to work independently and to effectively prioritize tasks.
+ Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines.
+ Knowledge of applicable regulatory requirements, including local regulations, , SOPs and company's Corporate Standards.
+ Understanding of regulated clinical trial environment and knowledge of drug development process.
+ Ability to establish and maintain effective working relationships with coworkers, managers and clients
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
+ Serve as Single Point of Contact (SPOC) in assigned studies for investigative sites, RSU Team Lead, Clinical Operations, Feasibility, Site Identification, Project Leadership and GICS. Ensure adherence to standard operating procedures (SOPs), work instructions (WIs), quality of designated deliverables and to project timelines. Where applicable, act as a Country Lead for projects with no regional Lead assigned.
+ Perform Regulatory, Start-up and Maintenance activities according to applicable regulations, SOPs and work instructions.
+ Prepare site regulatory documents, reviewing for completeness and accuracy.
+ Review, prepare and negotiate site contracts and budgets with sites, if applicable.
+ Ensure accurate completion and maintenance of internal systems, databases and tracking tools with project specific information.
+ Ensure contracts are fully executed, regulatory documents and approvals are granted, IP Release authorized and specific project deliverables are completed.
+ Review and provide feedback to management on site performance metrics.
+ Review, establish and agree on project planning and project timelines. Ensure overall project efficiency and adherence to project timelines. Ensure monitoring measures are in place and implement contingency plan as needed.
+ May contribute to the collection, interpretation, analysis and dissemination of accurate regulatory intelligence to support assigned studies and wider company, as required.
+ May assist in pre-award activities including bid defenses, proposals and oversights of the scope of work at country level.
+ May provide input into contract and budget template development.
+ May support importation activities.
+ May have direct contact with sponsors on specific initiatives.
+ May act as Local Regulatory, Ethics and Contract Expert and reviewer of ICF.
+ May act as mentor, and prepare and deliver country-specific training, for less experienced staff.
+ May participate in feasibility and/or site identification activities.
+ May perform Site Selection Visits if a trained monitor.
**Job Requirements:**
+ Bachelor's Degree in life sciences or a related field and 3 years' clinical research or other relevant experience; or equivalent combination of education, training and experience.
+ In-depth knowledge of clinical systems, procedures, and corporate standards.
+ Good negotiating and communication skills with ability to challenge, if applicable.
+ Effective communication, organizational, and interpersonal skills.
+ Ability to work independently and to effectively prioritize tasks.
+ Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines.
+ Knowledge of applicable regulatory requirements, including local regulations, , SOPs and company's Corporate Standards.
+ Understanding of regulated clinical trial environment and knowledge of drug development process.
+ Ability to establish and maintain effective working relationships with coworkers, managers and clients
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
This advertiser has chosen not to accept applicants from your region.
0
Site Budget Specialist (Clinical Trials)
ThermoFisher Scientific
Posted 21 days ago
Job Viewed
Job Description
**Work Schedule**
Standard (Mon-Fri)
**Environmental Conditions**
Office
**Job Description**
**Job Description**
At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future.
**Job Title:** **Associate Investigator Grants Analyst**
**Summarized Purpose:**
Prepares, reviews and finalizes global investigator grant budget and
Standard (Mon-Fri)
**Environmental Conditions**
Office
**Job Description**
**Job Description**
At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future.
**Job Title:** **Associate Investigator Grants Analyst**
**Summarized Purpose:**
Prepares, reviews and finalizes global investigator grant budget and
This advertiser has chosen not to accept applicants from your region.
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