Clinical Research

• Accountable for the full spectrum of investigator engagement from identification and qualification through enrollment, and support database lock, and study closeout
• Serve as a clinical trial scientific ambassador, ensuring investigators deeply understand protocol intent, scientific rationale, and patient eligibility requirements
• Develop and sustain strategic, high-trust relationships with investigators that span trials and therapeutic areas
• Influence enrollment by co-creating tailored recruitment strategies aligned with site capabilities, patient population realities, and study objectives
• Proactively find opportunities to reach new patients, accelerate enrollment and increase impact at priority sites
• Capture and elevate critical insights from sites to optimize feasibility, protocol design, and study conduct
• Lead site-level strategy and risk planning to ensure strong and predictable enrollment and data delivery
• Collaborate across functions and with vendor partners to resolve operational barriers
• Maintain advanced understanding of local treatment paradigms and standard of care to influence strategic country/site selection and protocol localization

Clinical Trial Liaison – Clinical Research Lead

• Accountable for the full spectrum of investigator engagement from identification and qualification through enrollment, and support database lock, and study closeout
• Serve as a clinical trial scientific ambassador, ensuring investigators deeply understand protocol intent, scientific rationale, and patient eligibility requirements
• Develop and sustain strategic, high-trust relationships with investigators that span trials and therapeutic areas
• Influence enrollment by co-creating tailored recruitment strategies aligned with site capabilities, patient population realities, and study objectives
• Proactively find opportunities to reach new patients, accelerate enrollment and increase impact at priority sites, including for example, novel site models, community-based research initiatives etc
• Capture and elevate critical insights from sites to optimize feasibility, protocol design, and study conduct
• Lead site-level strategy and risk planning to ensure strong and predictable enrollment and data delivery
• Leverage performance metrics to anticipate issues, intervene decisively, and maintain momentum toward clinical milestones
• Drive inspection readiness as a continuous discipline across sites
• Collaborate across functions and with vendor partners to resolve operational barriers, ensuring delivery with speed and quality
• Maintain advanced understanding of local treatment paradigms and standard of care to influence strategic country/site selection and protocol localization
• Provide oversight and quality assurance for vendor monitoring, escalating risks proactively
• Cultivate a portfolio of strategically aligned, high-impact investigators who consistently prioritize client trials
• Enable an exceptional investigator experience by being a responsive, knowledgeable, and valued scientific partner
• Collaborate cross-functionally (e.g., Medical, Clinical, Study Delivery) to align on trial and site priorities, troubleshooting challenges with urgency and creativity
• Conduct data-informed site prospecting and prioritization, contributing to trial competitiveness and regional strategic execution
• Maintain scientific fluency and therapeutic expertise to lead meaningful, solutions-focused discussions with site personnel
• Act as a key liaison between field teams, vendors, and investigators, ensuring alignment, shared purpose, and continuous knowledge transfer
• Partner closely with field team colleagues to elevate the investigator and site experience, ensuring seamless collaboration and improving enrollment outcomes and Investigator relationships

• In collaboration with other members of the clinical research site team, works to support source document requirements for assigned studies.
• Creation of source documents that will follow GCP Guidelines and 21 CFR Part 11 Compliance in addition to internal SOPs.
• Create templates, worksheets, supplemental source for visits based on detailed review of protocol-defined exams, tests, evaluations, and assessments.
• Initial creation of source documents will use all available protocol specific documents (i.e., current IRB approved protocol, blank or annotated CRF, Sponsor provided source templates/worksheets, or reference manuals) to create a source document that is accurate and complete and to ensure that the source document is equipped to record all the required data for the visit.
• Creating, maintaining, updating, control, and release source documents, including paper and electronic source documents in line with the study protocol, and relevant sponsor guiding documents.
• Reviewing draft source and ensuring it is accurate and complete and to ensure that the source document is equipped to record all the required data for the trial.
• Coordinating initial source review and update process.
• Filing, maintaining, distributing, organizing, and archiving source documents for each clinical trial.
• Updating current source documents according to new clinical study protocol amendments.
• Activating studies and visits at the appropriate time.
• Supporting Quality Control (QC) of source documents before it goes to the users.
• Attending all relevant meetings to stay up to date with upcoming studies, progress on current studies, and studies closing out.
• Maintaining a single tracker for the department to track source document design activities and the status of the activities.
• Maintaining version control of all source documents.
• Managing daily communication with site staff and other internal departments.
• Remaining up to date with all assigned Clinical Study Protocol for study.
• Developing and maintaining excellent working relationships with internal and external clients to understand and meet their needs in line with company policies and procedures.
• Maintaining a positive, results-oriented work environment, building partnerships within the team and across the organization at large, and modeling teamwork.
• Participating in continuing education activities to maintain current knowledge of source document design and relevant software.
• Performing all other duties that may be requested or assigned.

Clinical Research Source Development Coordinator

• Serve as a member of the central services team to deliver pharmaceutical support.
• Ensure delivery of therapeutic medication monitoring, EMR regimen build and review, protocol management.
• Provide drug information, dosing, monitoring, and education for safe medication therapy for patients in clinical trials.
• Collaborate with Research Department staff for quality patient care.
• Perform administrative and communication responsibilities for clinical trials.
• Support the development of new research regimen builds and inquiries.

Oncology Clinical Research Pharmacist

• Leads Life Extension Clinical Research and ensures studies are conducted in a timely, quality driven manner while following all applicable guidelines
• Provides overall leadership to LECR and staff by clearly communicating goals and expectations and driving productivity with a sense of urgency while ensuring 100% compliance with rules and regulations.
• Ensure all clinical trial projects (internal and external), to include project management, tracking and reporting trial progress and monitoring test item expiration dates in relation to project timelines
• Management and oversight of research projects and laboratory components of studies; develops appropriate study design and establishes accurate timelines; collaborates on statistical plans and data analysis
• Prepares and/or supervises the preparation of the Protocol, Informed Consent and associated documentation for clinical studies and assures necessary project approvals from an Institutional Review Board (IRB) are obtained
• Primary point of contact for the IRB
• Prepares and manages all LE Clinical Research budgets
• Sets priorities for all staff to assure project timelines are met, including active promotion of clinical research initiatives, i.e. use of social media
• Assures all applicable regulations are implemented and followed; supervises management of data files and confidential information; follows established SOPs, i.e. for appropriate document destruction
• Responds to inquiries from individuals seeking funding or product donations, and if warranted, presents project and recommendations to administration
• Monitors progress of ongoing external projects that received Life Extension support and/or donated materials, assuring resupply so materials do not expire without replacement during a project
• Seeks out ways to employ innovative technology to optimize organization and individual efficiency and performance
• Proactively drives the effort to achieve the goal of creating an impactful Clinical Center of Excellence.

Director, Clinical Research

• Full accountability for country-level study delivery and performance
• Serve as the client’s voice within Civia, ensuring their priorities, timelines, and standards are understood and met across all functions
• Maintain disciplined oversight of start-up, recruitment, regulatory progress, data quality, and site performance
• Drive immediate cross-functional action when performance deviates from plan
• Lead structured governance routines with clarity, transparency, and solution orientation
• Ensure ongoing audit and inspection readiness across all study activities

Clinical Trial Manager

• Responsible for study coordination and data management with a focus on managing subject recruitment and enrollment
• Maintain site compliance for all clinical trial activities and regulations
• Complete all relevant Profound Research required training in a timely manner
• Educates and directs protocol compliance with physicians and staff
• Ensure good documentation practices are applied by all team members
• Communicate effectively and professionally with coworkers, leadership, study subjects, sponsors, CROs, and vendors
• Acts as a patient advocate
• Collaborates with scheduling staff and the physician to assure appointments are scheduled correctly and treatment orders are written and delivered

Clinical Research Coordinator, RN

• Responsible for the performance of the research study under the medical supervision of the Principal Investigator and the research director
• Overall successful implementation and ongoing site management of the research studies
• Provide coverage in clinics when research staff are out of the office
• Precept new research staff in clinics
• Assist with research projects assigned by the Senior Clinical Research Coordinator III

RN Clinical Research Coordinator III – Drug Development Unit

• Conduct clinical studies according to FDA/GCP and ICH regulations and guidelines.
• Provide medical care to patients, always ensuring patient safety comes first.
• Schedule subject visits within protocol windows, ensuring scheduling capacity is maximized.
• Perform all defined study activities (i.e., informed consent, screening, and protocol procedures which include but are not limited to vital signs, pregnancy tests, height, weight, ECG's, etc.).
• Record all patient information and results from tests as per protocol on required forms.
• Where required, may complete IP accountability logs and associated information.
• Reports suspected non-compliance with relevant site staff.
• Ensures that IRB approval is obtained prior to study initiation and IRB requirements are met throughout the study.
• Promotes the company and builds a positive relationship with patients to ensure retention.
• Attend site initiation meetings and all other relevant meetings to receive training on protocol.
• May be required to call patients, do patient bookings and follow-up calls to confirm bookings or provide information or results.
• Logs/complete information on sponsor systems and ensures all information provided is accurate (i.e., case report forms, EDC, etc.) and ensures it is completed within timeframe.
• Gather and maintain source documents, updates patient files and notes, always ensuring relevant and most up to date information is recorded.
• Adhere to company COP/SCOP.
• May be required to dispose of waste according to standards and assist in keeping a general neat appearance of the facility.

Traveling Clinical Research Coordinator II

• Recruit, screen, and provide research-related services, interventions, and evaluations per protocol for participants enrolled in OB/GYN clinical research studies under the direction of the Principal Investigator (PI).
• Provide initial and ongoing informed consent with participants and families.
• Schedule study visits and procedures and follow-up study visits per protocol visit windows.
• Administer investigational product per protocol.
• Perform study-related procedures such as collection of vital signs, phlebotomy, and other procedures per protocol as delegated by the PI and in accordance with training and experience.
• Compile and maintain research progress notes and source documents and record data for each study participant in accordance with the research protocol.
• Monitor participants’ unexpected and adverse events, laboratory, radiology, and other procedure test results, and report to Investigator, sponsor, and IRB (Institutional Review Board) as appropriate.
• Collect and report study data on paper Case Report Forms or in electronic data capture systems per protocol, including query resolution.
• Prepare and submit documents to the Institutional Review Board(s) and other research review boards and committees as applicable and according to regulatory and institutional requirements.
• Educate patients, families, and staff in regard to clinical research activity.

Clinical Research Associate

• Ability to phone screen patients or caregivers in caring and empathetic manner.
• Document patient information correctly in the computer database.
• Schedule/reschedule patient screen and prescreen appointments.
• Manage incoming calls from patients interested in taking part in research studies.
• Evaluate eligibility of potential subjects through methods such as screening interviews, reviews of medical records, or discussions with site clinic staff.
• Learn and maintain knowledge regarding clinical research studies including inclusion and exclusion criteria for different studies.
• Record contact status of patients and document information in the database.
• Review, call and update sponsor patient portals as needed.
• Perform all other duties that may be requested or assigned.

Clinical Research Patient Recruiter

• Working cross-functionally to conduct gap analyses in clinical evidence and recommending strategies in line with business goals
• Providing leadership for the conduct of clinical research for product approval, post-market clinical follow-up, and market adoption or development
• Ensuring research plans are scientifically valid, meeting regulatory requirements, and are conducted within ethical guidelines
• Ensuring audit readiness and participating in related activities, e.g., serving as a subject matter expert
• Setting and communicating strategy, direction, priorities, and goals in partnership with the CRMS Leadership Team
• Serving as the ENT Clinical Research representative for enterprise councils and communities of practice
• Creating and maintaining a culture of ownership and accountability
• Managing performance, developing talent, and fostering engagement and inclusion through 1:1s, feedback, coaching, and delegation
• Setting and maintaining the budget and resourcing for the clinical research program and team
• Advancing ways of working and operational efficiency, including the use of AI-enabled tools
• Communicating business and operational developments up, down, and across
• Preparing reports and presentations for internal and external stakeholders for projects and budgets, integrating information from multiple sources

Senior Clinical Research Manager

• The Clinical Research Lead (CRL) is a strategic, field-based scientific leader responsible for driving the execution of Lilly clinical trials through exceptional investigator engagement and site performance management.
• Accountable for the full spectrum of investigator engagement from identification and qualification through enrollment, and support database lock, and study closeout
• Serve as a clinical trial scientific ambassador, ensuring investigators deeply understand protocol intent, scientific rationale, and patient eligibility requirements
• Develop and sustain strategic, high-trust relationships with investigators that span trials and therapeutic areas
• Influence enrollment by co-creating tailored recruitment strategies aligned with site capabilities, patient population realities, and study objectives
• Proactively find opportunities to reach new patients, accelerate enrollment and increase impact at priority sites, including novel site models, community-based research initiatives etc
• Capture and elevate critical insights from sites to optimize feasibility, protocol design, and study conduct
• Lead site-level strategy and risk planning to ensure strong and predictable enrollment and data delivery
• Leverage performance metrics to anticipate issues, intervene decisively, and maintain momentum toward clinical milestones
• Drive inspection readiness as a continuous discipline across sites
• Collaborate across functions and with vendor partners to resolve operational barriers, ensuring delivery with speed and quality
• Maintain advanced understanding of local treatment paradigms and standard of care to influence strategic country/site selection and protocol localization
• Provide oversight and quality assurance for vendor monitoring, escalating risks proactively
• Cultivate a portfolio of strategically aligned, high-impact investigators who consistently prioritize Lilly trials
• Enable an exceptional investigator experience by being a responsive, knowledgeable, and valued scientific partner
• Collaborate cross-functionally (e.g., Medical, Clinical, Study Delivery) to align on trial and site priorities, troubleshooting challenges with urgency and creativity
• Conduct data-informed site prospecting and prioritization, contributing to trial competitiveness and regional strategic execution
• Maintain scientific fluency and therapeutic expertise to lead meaningful, solutions-focused discussions with site personnel
• Act as a key liaison between field teams, vendors, and investigators, ensuring alignment, shared purpose, and continuous knowledge transfer
• Partner closely with field team colleagues to elevate the investigator and site experience, ensuring seamless collaboration and improving enrollment outcomes and Investigator relationships
• Represent Investigator Engagement with regulatory agencies, ethics committees, and national research organizations in countries/territory
• Influence the clinical trial ecosystem to improve regulatory agility and operational feasibility
• Ensure that local requirements are translated into compliant, efficient trial execution and that Lilly’s internal processes reflect evolving country landscapes
• Partner with leadership to identify and align regional initiatives and contribute to enterprise-wide clinical development success

Associate Director – Clinical Research Lead, Oncology

• Conduct and coordinate all aspects of clinical trial activities at the site.
• Perform phlebotomy on patients, following proper clinical and safety protocols.
• Recruit, screen, and enroll study participants according to inclusion/exclusion criteria.
• Schedule and conduct study visits, ensuring adherence to protocol requirements.
• Accurately collect, process, and ship biological samples per study-specific guidelines.
• Complete and maintain study documentation, including source documents, regulatory binders, and informed consent forms.
• Perform timely and accurate data entry into electronic data capture systems (EDC).
• Communicate effectively with sponsors, monitors, and other research team members.
• Ensure compliance with GCP, ICH, FDA, and IRB regulations.
• Assist in monitoring visits and audit preparation as needed.

See all jobs on JobTailor

Clinical Trial Liaison – Clinical Research Lead

Clinical Trial Liaison – Clinical Research Lead

Clinical Research Source Development Coordinator

Oncology Clinical Research Pharmacist

Director, Clinical Research

Clinical Trial Manager

Clinical Research Coordinator, RN

RN Clinical Research Coordinator III – Drug Development Unit

Traveling Clinical Research Coordinator II

Clinical Research Associate

Clinical Research Patient Recruiter

Senior Clinical Research Manager

Associate Director – Clinical Research Lead, Oncology

Clinical Research Coordinator