6,509 Remote Clinical Research Jobs (August 2026)

At Parexel, we strive to enhance global health through clinical trials and innovative solutions. We value personal contributions toward developing therapies for patients, seeking individuals who are proactive and passionate about improving processes. The Clinical Payments Specialist role in Warsaw involves payment tracking, document coordination, and collaboration with external partners. Essential skills include clinical administration experience and proficiency in Excel. We offer a premium salary and attractive benefits, alongside a supportive work environment focused on teamwork and innovation.

Posted 1 week ago

When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference. Parexel FSP is looking for a Clinical Trial Coordinator with experience with budget negotiation. This position is a hybrid position with 1-day minimum onsite requirement in Kirkland, Quebec. Job Title: Clinical Trial Coordinator (CTC) Position Purpose: The Clinical Trial Coordinator (CTC) is responsible for the following: • Supports the Clinical Research Manager (CRM) and other team members through the life cycle of the study from study start up to study closure. Organizational Relationships: • Reports to Parexel assigned Line Management with day-to-day direction from Client. Refer to Organizational Chart for details regarding assigned role and associated reporting structure. Primary Responsibilities: • Trial and site administration: o Tracking (e.g., essential documents) and reporting (e.g., Safety Reports). o Ensure collation and distribution of study tools and documents. o Update clinical trial databases (CTMS) and trackers. o Clinical supply non‐clinical supply management, in collaboration with other country roles. o Manage Labeling requirements and coordinate/sign translation change request. • Document management: o Prepare documents and correspondence. o Collate, distribute/ship, and archive clinical documents. o Assist with electronic Trial Master File (eTMF) reconciliation. o Updating manuals/documents (e.g., patient diaries, instructions). o Document proper destruction of clinical supplies. o Prepare Investigator trial file binders. o Execute eTMF Quality Control Plan. o Obtain translations of documents. • Regulatory Site Start Up responsibilities: o Provide to and collect from investigators forms/lists for site evaluation/validation, site start‐up and submissions in a timely manner. o Obtain, track and update study insurance certificates. o Support preparation of submission package for Institutional Review Board (IRB) / Ethics Review Committee (ERC) and support regulatory agencies submissions. o Publish study results for Global Clinical Trial Operations (GCTO) and Regulatory Affairs (RA) where required per local legislation. • Budgeting, Agreement and Payments: Collaborate with finance/budgeting representatives for: o Development of country and site budgets (including Split site budget). o Tracking and reporting of negotiations. o Maintenance of tracking tools. o Working knowledge of contract development, negotiation, approval, and maintenance (e.g., Clinical Trial Research Agreements (CTRAs)). o Updating and maintenance of contract templates (in cooperation with Legal Department) o Payment calculation and execution (investigators, vendors, grants o Ensuring compliance with financial procedures. o Monitoring and tracking adherence and disclosures. o Budget closeout. o Obtain and process Foreign Corrupt Practices Act (FCPA) documentation in a timely manner. • Meeting Planning: o Organize meetings (create track study memos/letters/protocols). o Support local investigator meetings (invitations, prepare materials, select venue, support where applicable). • Completes training assigned by Client and/or EP, as necessary, including general training requirements, SOPs, and system and process related training. • Adheres to EP and Client SOPs and processes. Education and Certification: • B.A./B.S. (Life Sciences preferred) or equivalent healthcare experience. Skills and Experience: • Minimum 1-2 years in Clinical Research or relevant healthcare experience. Note - Specific experience requirements may vary depending on the Country • Good understanding of Global, Country/Regional Clinical Research Guidelines and ability to work within these guidelines. • Hands on knowledge of Good Documentation Practices. • Good IT skills (Use of MS office, use of some clinical IT applications on computer) and ability to adapt to new IT applications. Strong MS Excel skills required. • International Committee on Harmonization (ICH) ‐ Good Clinical Practice (GCP) knowledge appropriate to role. • Effective time management, organizational and interpersonal skills, conflict management. • Effective communication with external customers (e.g., sites and investigators). • High sense of accountability / urgency. Ability to set priorities and handle multiple tasks simultaneously in a changing environment. • Works effectively in a matrix multicultural environment. Ability to establish and maintain culturally sensitive working relationships. • Demonstrates commitment to Customer focus. • Able to work independently. • Proactive attitude to solving problems / proposing solutions. • Positive mindset, growth mindset, capable of working independently with assigned tasks. • Contributes to CTC team knowledge by acting as buddy /mentor and sharing best practices as appropriate/required. Language Skills: • Fluent in Local Languages and business proficient in English (verbal and written) and excellent communication skills. #LI-KW1

Posted 3 weeks ago

RayzeBio, a subsidiary of Bristol Myers Squibb, is seeking a Clinical Trials Manager for their Clinical Operations. This role focuses on the oversight, planning, and execution of clinical studies to ensure compliance with industry standards and regulations. The Clinical Trials Manager will lead cross-functional teams, manage budgets, and address operational risks, making a significant impact on the company's goal to develop innovative cancer therapies. Candidates should have 5-7 years of experience in clinical operations and a related degree.

Posted 1 week ago

Worldwide Clinical Trials, a global mid-size CRO, is seeking a Senior Clinical Research Associate for the Midwest/Southeast regions (remote). This role calls for a professional who can manage clinical research activities at various sites, collaborating with diverse therapeutic areas. The company offers a supportive work environment, prioritizing professional development and diversity. Candidates must bring strong communication, organizational skills, and experience in CNS or neurology.

Posted 1 week ago

Syneos Health is seeking a Senior CRA to join their Clinical Solutions team. In this role, you'll ensure compliance with regulatory guidelines while performing site management tasks. You'll collaborate with a dynamic team dedicated to delivering quality solutions for drug development and commercialization. The position requires strong interpersonal skills, knowledge of clinical practices, and the ability to handle significant travel. Syneos Health prioritizes career development and an inclusive culture, making it an ideal environment for those passionate about advancing healthcare.

Posted 1 week ago

PSI CRO is seeking a Senior Clinical Research Associate to join its dynamic team. This role involves direct communication with project stakeholders and maintaining relationships with clinical sites. You will ensure compliance with the highest standards of clinical research while focusing on subjects' rights and safety. Ideal candidates should have significant experience in on-site monitoring, particularly in Oncology trials, and be proficient in English. This position offers the opportunity to be involved in all aspects of clinical studies while supporting a company that prioritizes its employees.

Posted 1 week ago

WEP Clinical is seeking a Senior Clinical Research Associate to oversee clinical monitoring and site management. This remote role requires expertise in clinical research, compliance with regulations, and strong relationship-building skills. The ideal candidate will have 5-7 years of experience, preferably in a leadership capacity, and must be detail-oriented and adaptable. Responsibilities include supervising monitoring processes, contributing to study document design, and ensuring protocol adherence. Join a mission-driven team that supports drug development and improves patient access to treatments.

Posted 2 weeks ago

JOB SUMMARY The Senior Clinical Research Associate is responsible for the site management, site monitoring and close[1]-out of assigned clinical trials investigator sites to ensure patient safety and quality study execution in accordance with applicable prevailing laws, Good Clinical Practices, and Pfizer standards. The Senior Clinical Research Associate I role is accountable for site management and monitoring, managing investigator site relationships to ensure effective delivery of clinical trials (e.g. enrollment, database release), to safeguard the quality of investigator sites (e.g. patient safety, site quality and compliance with GCP), to maintain investigator and site staff engagement and satisfaction, and to enhance the company’s image with its external stakeholders. The Senior Clinical Research Associate I is responsible for the resolution of all protocol-related issues for assigned investigator sites and will work closely with the Site Care Partner, and other members of the study team, as required, in activities associated with the set-up, running and close out of sites in a clinical trial. JOB RESPONSIBILITIES Responsible for investigator site management and monitoring for assigned sites: Clinical Trial Monitoring: • Ensure proper conduct of clinical trials in accordance with the Study Monitoring Plan and applicable prevailing laws, Good Clinical Practices, and Pfizer standards to achieve project goals, timelines and quality • Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites from site initiation through to database lock, ensuring relevant timelines and quality deliverables are met • During study conduct, serve as the primary point of contact for assigned investigator sites. Work in partnership with and/or escalate to the SCP to ensure quality of site delivery • Interface with the study team as needed, facilitate information flow between members of the study team, vendors and assigned investigator sites • Partner with SCP to perform investigator site development, coaching and training of site personnel to ensure ongoing compliance with protocol and the safeguarding of patients; provide protocol training to, and address protocol related questions from the investigator site staff when required, including discussions on known/anticipated operational and clinical trial risks • Attend investigator meetings when required (virtual or F2F). • Provide enrollment support and ensure progress by responding to site activation and recruitment issues from investigators. Partner with SCP and the study team to define and support recruitment initiatives at site level • Conduct onsite, remote/electronic monitoring as needed for study site initiation, routine monitoring and study site closure activities and ensure these are conducted accordance to the Study Monitoring Plan, SOPs and commensurate with emerging issues and technologies. • Monitor site level AEs and SAEs and collaborate with the Drug Safety Unit and follow-up with investigators sites, as needed, to bring SAE reports required information to resolution • Submit all required reports, documentation, updates and tracking within required timeframes, including but not limited to Trial Master File documentation, site reports, site follow up letters, protocol deviations, patient recruitment, clinical supply management, study progress and metrics • Identify and resolve investigator site issues within required timeframes; agree and develop corrective and preventative actions with investigator and site personnel to close open issues and to prevent recurrence/persistence of issues • Resolve data queries within required timelines, prepare investigator site close-out plan and conduct close-out activities within required timelines • Ensures adequate oversight of the investigational product at the investigator site, including receipt, handling, accounting, storage conditions, and destruction activities. • Support database release as needed • May undertake the responsibilities of an unblinded monitor where required Clinical/Scientific and Site Monitoring Ris k: • Maintain thorough understanding of the product, protocol and therapy area in sufficient details to have appropriate discussions with the investigator and site team • Interact with investigator site heath care professionals in a manner which enhances Pfizer’s credibility, scientific leadership and in order to facilitate Pfizer’s clinical development goals • Support the study clinician in ensuring patient safety, eligibility and providing clinical guidance to investigators • Drive Quality Event remediation, when applicable • Serve as a point of contact for audit conduct, and drive Audit Observation CAPA development andchecks, when applicable. Other: • Mentor/train Clinical Research Associates as assigned • Serve as an SME for CRA-related processes • Participate in regional or local working groups/process improvement initiatives • Perform activities under guidance of a Site Care Partner prior to site activation e.g. feasibility and site selection, PTA, coordination of site activation checklist items, ICD finalization, SIV (as applicable), including management of issues that may compromise time to site activation • Conduct co-monitoring activities as requested QUALIFICATIONS • Bachelor’s degree in life sciences or professional degree in life sciences such as nursing, pharmacy, medical background or equivalent • Extensive knowledge of clinical trial methodologies, ICH/GCP, FDA and local country regulations • Monitoring Experience: Minimum 3 years relevant experience in clinical research site monitoring (preferably 2 years in Oncology) • Preferred therapeutic experience in Oncology, Vaccines, Internal Medicine or Infectious Diseases • Global clinical trial experience • Must be fluent in English and in the native language(s) of the country they will work in PHYSICAL/MENTAL REQUIREMENTS Advanced knowledge of clinical research and development processes and ability to gain command of process details • Demonstrated knowledge of global and local regulatory requirements • Advanced understanding of key operational elements of clinical research (e.g., monitoring, data acquisition and cleaning, reporting, etc.) • Advanced knowledge in disease and technical areas pertaining to clinical studies, including knowledge of company direction, investigational product(s), and associated development plan(s) • Demonstrated ability to support sponsor regulatory interactions/inspections • Demonstrated knowledge of the processes around protocol design and feasibility assessment • Demonstrated understanding of region/country, culture, and medical practice and how they affect clinical trial delivery • Proven ability to work in a matrix team environment with the ability to influence, drive / lead and work through others for successful delivery of clinical trial • Proven ability to evaluate, interpret and present complex issues and data to support risk management and mitigation • Effective verbal and written communication skills in relating to colleagues and associates both inside and outside of the organization • Significant travel (60-80%) within area is required. May require some international travel and some weekend travel • Valid driver’s license and passport required ORGANIZATIONAL RELATIONSHIPS • Partners with Site Care Partner and Country SOM • Reports to Director of Clinical Site Operations, or Director of Site Management and Monitoring, or Site Care Partner III in some countries • When required Partners with other Study Team members e.g. Clinician, Recruitment Specialist, Clinical Data Scientist • Act as a mentor for Clinical Research Associates • Partner with other functional lines if engaged in a workstream/ LDT/ SME role Work Location Assignment: Remote Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates. To learn more about acceptable and prohibited uses of AI during the recruitment process, please review our candidate AI-use guidelines available on Pfizer Careers . #xa;Medical

Posted 3 weeks ago

Join Immatics and shape the future of cancer immunotherapy; one patient at a time! Immatics is committed to making a meaningful impact on the lives of patients with cancer. We are the global leader in precision targeting of PRAME , a target expressed in more than 50 cancers. Our cutting-edge science and robust clinical pipeline form the broadest PRAME franchise with the most PRAME indications and modalities, spanning TCR T-cell therapies and TCR bispecifics. Why Join Us? Innovative Environment: Help to pioneer advancements in cancer immunotherapy. Collaborative Culture: Be part of a diverse team dedicated to your professional growth. Global Impact: Contribute to therapies that make a lasting impact on patients globally. Role Overview: We are seeking a Senior Clinical Research Associate (CRA) to support our Clinical Operations team. The Senior CRA will be responsible for overseeing clinical trial site management and monitoring activities to ensure compliance with ICH-GCP, regulatory requirements, and company SOPs. In this role, you will partner closely with clinical sites and cross-functional teams to support high-quality study execution, patient recruitment, and operational excellence across clinical trials. Reports to : Director, Team Lead Site Operations Location : Fully Remote Salary Range: $120,000 to $135,000 Basic Qualifications: Bachelor’s degree in life sciences, nursing, or a related field 4+ years of on-site monitoring experience within the pharmaceutical or biotechnology industry, including all clinical monitoring visit types Strong knowledge of ICH-GCP, FDA, EMA, and applicable clinical trial regulations Demonstrated experience managing clinical trial sites, monitoring activities, and clinical trial documentation Proficiency with clinical trial systems and tools (e.g., CTMS, eTMF, Microsoft Office) Preferred Qualifications: Experience in oncology clinical trials or related therapeutic areas Advanced presentation, organizational, and stakeholder management skills Experience mentoring or training junior CRAs and supporting cross-functional clinical operations activities Demonstrated ability to drive quality, efficiency, and continuous improvement initiatives in clinical operations Strong understanding of clinical trial recruitment strategies, data capture, and site engagement best practices Experience contributing to global harmonization, process optimization, or operational innovation initiatives In this role you will: Conduct all clinical monitoring activities, including site qualification, initiation, routine monitoring, and close-out visits Support site feasibility, site selection, and ongoing site management activities throughout the clinical trial lifecycle Review clinical trial progress, patient recruitment, and data quality metrics, and implement actions to support study objectives Maintain accurate and timely monitoring documentation, including trip reports and trial master file records Collaborate with vendors, clinical sites, and cross-functional teams to support study execution and operational compliance Participate in investigator meetings, clinical trial documentation development, and study team meetings Mentor junior CRA team members and contribute to continuous improvement of clinical operations processes and procedures Travel required: Willingness to travel up to 75%. Valid Driver's License preferable. Qualified candidates will participate in a structured interview process, which includes: An initial recruiter phone screen (conducted via video) A recruiter-facilitated introduction and interview with the hiring leader and key stakeholders (via video) A final-stage interview, which may include an in-person meeting at our U.S. Headquarters in Houston, TX What do we offer? At Immatics, we believe in investing in our team’s health, safety and well-being. Here’s what you can expect if you join Immatics Comprehensive Benefits : Competitive rates for Health, Dental, and Vision Insurance 4 weeks of vacation, granted up front each year and prorated for first and last year of employment. 12 company paid holidays 7 days of sick time 100% employer-paid life insurance up to at 1x annual salary, up to one hundred thousand dollars 100% employer-paid short- and long-Term disability coverage 401(k) with immediate eligibility and company match… The company will match 100% of your contributions up to 3% of your base salary for the first two years of employment, 4% for years 2-3 of employment, and up to 5% of your salary from the fourth year onward of continued employment. Partially paid parental leave for eligible employees. Additional voluntary employee-paid benefits and services, including accident, hospital indemnity, and critical illness insurance, as well as identity theft protection and pet insurance. Equal Employment Opportunity We are an equal opportunity employer and are committed to building a diverse and inclusive workplace. We consider all qualified applicants for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity or expression, national origin, ancestry, age, marital status, disability, genetic information, veteran status, or any other status protected by applicable law. Reasonable Accommodations We are committed to providing reasonable accommodations to individuals with disabilities and to applicants with sincerely held religious beliefs, practices, or observances. If you require assistance or accommodation during the application or interview process, please contact us at [email protected] . Work Authorization Applicants must be authorized to work in the United States without the need for current or future sponsorship. Visa sponsorships may be available for certain roles. Pre-Employment Requirements Employment is contingent upon successful completion of a background check, reference checks and pre-employment drug screening, where permitted by applicable law. For certain roles, additional screenings such as a credit check or motor vehicle record review may be required, where job-related and consistent with business necessity.

Posted 3 weeks ago

Caribou Biosciences is a leading clinical-stage CRISPR genome-editing biopharmaceutical company dedicated to developing transformative therapies for patients with devastating diseases. Our next-generation genome-editing technology enables superior precision to develop cell therapies that are armored to potentially improve activity against diseases. We believe the future of cell therapy is off-the-shelf, and we are advancing our pipeline of off-the-shelf, or allogeneic, cell therapies from our CAR-T cell therapy platform as readily available treatments for patients with hematologic malignancies and autoimmune diseases. Members of the Caribou herd open their minds to new ideas and welcome diverse perspectives. We proudly assert that teams do their best work when their members are personally engaged, their ideas are taken seriously, and contributions are recognized. Members of the herd work from our headquarters in Berkeley, California, or remotely. We are seeking a Clinical Trial Manager (CTM) to join our Clinical Operations group. You will be responsible for the operational execution and Sponsor oversight of global clinical trial activities from study start-up through study close-out. The CTM ensures trials are conducted in accordance with ICH-GCP, applicable country regulations, standard operating procedures, and study-specific protocols. The CTM will report to the Director of Clinical Operations. This position may be onsite, hybrid, or remote. Responsibilities: Study Management Manage operational activities related to all phases of clinical studies, including study/site feasibility, start-up, maintenance, and close-out Support study operational planning and execution, including site and vendor identification, evaluation, qualification, and oversight Implement operational strategies to support timely patient enrollment and maintain high standards for site monitoring and trial execution Manage operational aspects of clinical trials throughout the study lifecycle from study start-up through to Clinical Study Report completion Develop and manage study-specific operational tools, documentation, timelines, trackers, and communications, while coordinating cross-functional development and review of key study documents Manage trial-level operational risks, including identification, assessment, tracking, mitigation, and documentation to ensure compliance, and quality across trial activities Organize and prepare for study-related meetings, including agendas, minutes, presentations, and action items CRO and Vendor Oversight Provide Sponsor oversight of CRO performance related to site qualification, site initiation, monitoring, enrollment, data quality, sample logistics, and site close-out activities Review vendor performance, deliverables, key performance metrics, and governance activities to ensure contractual obligations and study expectations are met Collaborate with Supply Chain, CROs, and external vendors to support investigational product, laboratory, sample management, and study supply logistics Review and verify service provider deliverables and operational activities for quality and timeliness Data Review and Quality Oversight Perform ongoing Sponsor data review to identify trends and support query management, protocol deviation review, safety review, and issue resolution Review monitoring visit reports and, as appropriate, participate in co-monitoring, monitoring, or oversight visits. Support oversight of clinical site performance through review of study metrics, monitoring data, and trends Ensure all trial operations are executed within timelines and budgets while adhering to ICH-GCP, applicable regulations, and company procedures Trial Master File and Inspection Readiness Maintain and oversee the Trial Master File (TMF), ensuring completeness, quality, and continuous inspection readiness Review and/or approve site-specific documents, including informed consent forms, site budgets, monitoring reports, and other study documentation Support the preparation, conduct, and follow-up of audits and inspections, including site, vendor, and internal quality audits Cross-Functional Collaboration Provide timely updates on trial progress, operational risks, and mitigation strategies to stakeholders Support the development and implementation of study training for investigators, site staff, and internal teams Collaborate effectively with Clinical Development, Data Management, Biostatistics, Regulatory Affairs, Medical Monitoring, Drug Supply, Quality Assurance, Safety, and other cross-functional partners to ensure successful trial execution Support Clinical Operations process improvements, infrastructure development, and other strategic initiatives as assigned Requirements : BS degree in the life sciences with a minimum of 6+ years in Clinical Operations, with a MS degree in the life sciences with a minimum of 4+ years of Clinical Operations experience 3 years of Sponsor Clinical Trial Management experience Experience supporting complex global Phase III clinical trials Cell therapy or Oncology Experience Strong understanding of ICH-GCP, FDA, EMA, and applicable global regulatory requirements Demonstrated proficiency in technology use, documentation practices, and sound business acumen Advanced proficiency in Microsoft 365 (Word, Excel, PowerPoint, Outlook, and SharePoint) Strong attention to detail and a commitment to producing high-quality work Excellent written and verbal communication and interpersonal skills Ability to travel up to 20% based on business needs Nice-to-haves: Experience working in a fast-paced, dynamic start-up biotechnology environment Caribou compensation and benefits include: Comprehensive compensation package, which includes competitive salary, bonus, and equity for all employees Salary Range: $160,000 - $175,000; this represents the present low and high end of the Company’s pay range for this position; actual pay will vary based on various factors, including but not limited to location, skill, experience, and performance Generous paid vacation time, in addition to company-observed holidays Excellent medical, dental, and vision insurance 401(k) retirement savings plan, which includes matching employer contributions Employee stock purchase plan (ESPP) Tuition reimbursement program The benefits and stock purchase described above are subject to the terms and conditions of any governing plans, policies, practices, agreements, or other materials or documents as in effect from time to time, including but not limited to terms and conditions regarding eligibility. Caribou is an equal opportunity employer and does not discriminate based on race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical conditions, veteran status, sexual orientation, gender (including gender identity and gender expression), sex (which includes pregnancy, childbirth, and breastfeeding), genetic information, taking or requesting statutorily protected leave, or any other basis protected by law. In addition, Caribou prohibits the harassment of any individual on any of the bases listed above or any other characteristics protected under federal, state, or local laws. Legal authorization to work in the United States is required. In compliance with federal law, all persons hired will be required to verify identity and eligibility to work in the United States and to complete the required employment eligibility verification form upon hire. We do not accept unsolicited resumes or candidate submissions from staffing agencies. All agencies must have a valid written agreement with Caribou Biosciences, Inc. for service in place. Any resume or candidate submitted by a staffing agency without such an agreement in place will be considered unsolicited, and Caribou Biosciences, Inc. will not be obligated to pay any referral or placement fee.

Posted 2 days ago

Syneos Health is seeking a Clinical Trial Manager focused on project management to oversee clinical trials and ensure compliance with regulations. The ideal candidate will lead teams to achieve project milestones, manage site interactions, and mitigate risks throughout the trial process. This position requires strong leadership, communication, and problem-solving skills in a dynamic work environment. The role offers an opportunity to make a significant impact on clinical research initiatives and improve patient outcomes by working closely with various stakeholders.

Posted 3 days ago

About the Job Join Excelya, where Audacity, Care, and Energy define who we are and how we work. We believe in creating bold solutions and fostering an inclusive environment where collaboration and individual growth go hand in hand. This role is an exciting opportunity to contribute to a dynamic, ambitious team in Clinical Operations. You will play a critical part in driving innovation and making an impact in the clinical research space, while enjoying a stimulating professional environment that encourages personal and intellectual growth. Key responsibilities : Manage and maintain the Trial Master File (TMF/eTMF), ensuring completeness, accuracy, compliance, and inspection readiness throughout the study lifecycle. Coordinate TMF documentation activities, including collection, filing, tracking, and reconciliation of study documents from internal teams and CROs. Conduct TMF quality reviews and QC checks to ensure compliance with ICH-GCP requirements and company procedures. Ensure timely identification and resolution of missing, outdated, or incomplete study documentation. Oversee study document archiving activities in accordance with regulatory and company requirements. Support financial management of clinical studies, including purchase orders, invoices, budget tracking, commitments, and payment follow-up. Coordinate transparency reporting activities and maintain documentation required for compliance with local and international disclosure regulations. Provide operational support for clinical studies, including contract management, insurance renewals, clinical supply coordination, and maintenance of essential legal documents. Maintain and update clinical systems and tracking tools (CTMS, SAP, SharePoint, iCap, and related platforms) to ensure accurate study status reporting. Act as a key operational liaison between Clinical Research Managers, CROs, vendors, and internal stakeholders, supporting the successful delivery of clinical trials within quality, timeline, and regulatory requirements.

Posted 3 days ago