Clinical Research Associate Jobs

5 open positions found · Salary range: From $24

Clinical Research Associate

ClinoGenesis Research InstituteKerala, Kerala, India

From $202/yr

Clinical Research Associate (Trainee/Freshers Only) Organization: Clinogenesis Research Organization Location: Remote (India) Department: Clinical Operations Employment Type: Full-Time About the Role Are you a recent graduate eager to start a career in Clinical Research but finding it difficult to gain entry? Clinogenesis Research Organization is bridging the gap between graduation and professional success. We are offering an exclusive, entry-level Career Launchpad designed specifically for freshers. This is not just a job; it is a dedicated training program where we teach you the actual industry-required skills necessary to excel as a Clinical Research Associate (CRA). We transform your academic knowledge into practical, real-world expertise. Why Join Our Program? Skill-First Training: We bridge the gap between your degree and the job market by providing intensive training on industry-standard operations. Mentorship: Work directly with industry experts who are committed to your professional development. Hands-on Exposure: Gain practical experience in global clinical trial standards, moving beyond textbook theory. Clear Growth Path: A structured roadmap within a globally recognized organization designed to evolve you into a seasoned professional. Key Responsibilities Industry Skill Mastery: Actively participate in specialized training sessions to master clinical operations, documentation, and regulatory compliance. Site & Documentation Support: Learn to manage Trial Master Files (TMF), site files, and Case Report Forms (CRF) with accuracy. Protocol Compliance: Gain a deep understanding of ICH-GCP, ethical guidelines, and local regulatory requirements. Operational Assistance: Assist in the daily management of clinical trial activities and patient coordination under the guidance of senior mentors. Eligibility Criteria (Strictly Freshers) Education: B.Pharma, M.Pharma, D.Pharma, and all Life Sciences graduates (B.Sc/M.Sc in Biotechnology, Microbiology, Nursing, Biochemistry, or equivalent healthcare fields). Batch: 2024, 2025, and 2026 graduates (Final year students are highly encouraged to apply). Experience: Strictly 0 years. We are looking for fresh talent ready to be molded. Candidates with prior professional clinical research experience will not be considered. Skills: Exceptional communication, a high level of organization, and a genuine passion for building a long-term career in the life sciences industry. How to Apply If you are ready to transition from a student to a professional, we want to hear from you! Join our Fresher Intake Program and let us help you launch your clinical research career. #ClinicalResearch #CRA #FreshersHiring #PharmaJobs #LifeSciences #DPharma #BPharma #MPharma #CareerLaunchpad #JobSearch2026 #ClinicalTrials #EntryLevelJobs #HiringFreshers #clinicalresearchassociate Please mention the word POIGNANT and tag RMjE3LjE1Ni42NS4xNjY= when applying to show you read the job post completely (#RMjE3LjE1Ni42NS4xNjY=). This is a beta feature to avoid spam applicants. Companies can search these words to find applicants that read this and see they're human.

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Clinical Research Associate 2, Adelaide

Emerald ClinicalAdelaide, South Australia, Australia

From $160/yr

Who We Are Emerald Clinical Trials is a global leader in clinical research, partnering with over 160 biotech companies and 15 of the world’s top 20 pharmaceutical firms. Headquartered in Singapore, we combine scientific excellence with operational expertise to deliver end-to-end clinical trial solutions across all phases, offering Phase I-IV and real-world studies . With over 25 years of experience and a world-renowned focus in renal research , Emerald Clinical has helped drive medical breakthroughs through deep scientific insight, flawless execution, and an unwavering commitment to quality. Global Expertise. Local Insight. Real Impact. Emerald Clinical is where science, speed, and strategy come together to transform healthcare. For over 25 years, we have led the way in clinical research, combining global reach with deep Asia-Pacific expertise and unparalleled local insight to deliver smarter trials and stronger outcomes. Our 1000+ employees that span across Asia-Pacific, Europe, and the Americas are embedded in communities worldwide. We drive faster recruitment, deeper patient engagement, and meaningful results that move medicine forward. About The Role The Clinical Research Associate 2 is a member of the Clinical Operations group at Emerald Clinical . The Clinical Operations group is responsible for site management, monitoring tasks, and the operational support of clinical trials. The group allocates resources to projects as appropriate to assist with implementing project plans and to ensure compliance with regulatory requirements and Standard Operating Procedures (SOPs) Your Responsibilities * Coordinate the identification, feasibility assessment, and selection of investigators and sites to undertake the trial. * Complete all monitoring activities per the Monitoring Plan along with completing monitoring visit reports, accurately and within the predetermined timeframe. * Prepare, plan, organize, and conduct site evaluation visits and report on these visits to assist in site selection. * Prepare, submit, and/or liaise with regulatory specialist colleagues, regarding the preparation of regulatory packages, importation/exportation requirements, and updates of Ethics Committee packages. * Negotiate site budgets, coordinate for site contract execution, track invoicing, and ensure timely site payments. * Prepare, plan, organize, and conduct site initiation visits. * Develop and maintain appropriate monitoring tools and project-specific documents. * Motivate and train investigators to ensure that the trial site personnel have a good understanding of the protocol, investigational product, and requirements of the trial so they can fulfill their obligations to conduct the trial accurately and to deadlines. Collect, review, and approve essential documents from trial sites, to ensure quality and compliance, and code documents for Trial Master File (TMF) filing. * Reconcile contents of in-house TMF and site’s Investigator Site Files. * Coordinate distribution, tracking, handling, and destruction of investigational product and other trial supplies per site/trial requirements. * Maintain trial information using the clinical trial management system and any other tracking and reporting tools for the trial. * Support strategies to boost recruitment efforts. About You * Tertiary qualifications in a related science or health care discipline. * Previous experience in clinical trials within an academic, CRO, or pharmaceutical environment with more than 2 years' experience in on-site monitoring and site management experience is mandatory * Experience in Renal and/or Oncology clinical trials is a plus. * Demonstrate practical knowledge of ICH-GCP guidelines and global and local ethical and regulatory research requirements. * Display competence in the following technical areas: ethical and participant safety considerations, site start-up management, site conduct management, risk management, quality management, supply management, scientific concepts and clinical research design, and issue escalation management. * Demonstrate competence in the following business skill areas: negotiation and conflict resolution, critical thinking, problem-solving, decision making, and strategic thinking. * Demonstrate solid interpersonal communication, presentation skills, and flexibility to work well within a multi-disciplinary team both autonomously and with a wide range of varying stakeholders * Ability to be flexible and adaptable in the face of changing organizational priorities and ambiguous environments. * Ability and willingness to travel Why Join Us? At our core, Emerald Clinical Trials is committed to transforming clinical research by putting people first—both patients and our employees. By joining our team, you’ll be part of a global network of passionate professionals working together to deliver better research and outcomes for millions worldwide. Here’s What Makes Us Stand Out * Purpose-Driven Work: You’ll contribute to clinical trials that genuinely improve lives, with a focus on therapies in renal, cardiometabolic, and oncology. * Global Reach, Local Expertise: Our teams connect with local communities, building trust and meaningful engagement for every trial. * Collaboration and Innovation: Work in a culture that values diverse perspectives and creative solutions to solve global health challenges. What We Offer We understand that great work happens when people feel valued and supported. That’s why we provide: * Competitive Compensation: A tailored salary and benefits package to reflect your skills and experience. * Flexibility: Enjoy hybrid or remote working arrangements, depending on your location and role. * Career Growth: Access to a wealth of learning opportunities and a global network of scientific leaders to help you grow and develop in your role. * Employee Wellbeing: Participate in programs and initiatives designed to promote work-life balance, health, and team connection, including global engagement surveys, recognition programs, and team-building events. * Global Opportunities: Be part of a company with international reach, offering you exposure to diverse projects and clients. Interested? Apply now and help us achieve our mission to improve the health of millions worldwide. We are an equal-opportunity employer and encourage applications from all qualified candidates.

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Clinical Research Associate I

AbbVieSydney, NSW, AU

From $24/yr

Company Description About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube. Job Description Join AbbVie's Expanding Clinical Operations Team At AbbVie, we are committed to discovering and delivering innovative medicines that solve serious health issues today while addressing the medical challenges of tomorrow. We're looking for a Clinical Research Associate I (CRA I) to join our growing team in Australia and help advance clinical studies that have the potential to transform patient outcomes. This is an opportunity to become part of a growing team supporting a strong pipeline and diverse portfolio of clinical programs across multiple therapeutic areas, while building a long-term career with one of the world's leading biopharmaceutical companies. If you're looking for more than just your next role and want the opportunity to broaden your experience and contribute to innovative clinical development programs, we'd love to hear from you. KEY DUTIES AND RESPONSIBILITIES * Monitors activities conducted by clinical investigative sites as they relate to AbbVie clinical studies to ensure successful execution of the protocol. Ensures adherence to federal regulations and applicable local regulations, Good Clinical Practices (GCPs), ICH Guidelines, AbbVie Standard Operating Procedures (SOPs), Monitoring Plans, and quality standards in conducting clinical research. * Conducts site qualification, initiation, interim monitoring and study closeout visits for Phase 1-4 studies in accordance with applicable regulations, Good Clinical Practices (GCPs), ICH Guidelines, and AbbVie Standard Operating Procedures (SOPs) and business processes. * Overviews the overall activities of site personnel over whom there is no direct authority and motivates/influences them to meet study objectives. proactively manages the site and ensures action plans are put into place as needed to ensure compliance. Ensures regulatory inspection readiness at assigned clinical sites. * Ensures quality of data submitted from study sites and ensures timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel. * Ensures safety and protection of study subjects through compliance with the study monitoring plan, AbbVie SOPs, ICH Guidelines, and applicable regulations. * Trains study site personnel on the protocol and applicable regulatory requirements in collaboration with pertinent project team members. * Manage investigator payments as per executed contract obligations. Maintain and complete own expense reports as per local and applicable guidelines. * Identifies, evaluates and recommends new/potential investigators/sites on an ongoing basis. Potential sites may be identified through networking or internal AbbVie requests to assist in the placement of planned clinical studies with qualified investigators. * Report any adverse event within 24 hours as per AbbVie’s policies and procedures. * Proactively participate in AbbVie’s WHS programs, adhere to policies and promote a safe work environment at all times. * Adhere to AbbVie’s internal codes of conduct and compliance processes. * Other ad hoc duties such as administrative duties, as requested. Qualifications * Appropriate tertiary qualification, health related (e.g., Medical, Scientific, Nursing) preferred. * Minimum of 1 year of clinically related experience, of which a period of 6 months is preferable in clinical research monitoring. Experience in on-site monitoring of investigational drug or device trials are required. * Current in-depth knowledge and understanding of appropriate therapeutic indications as they relate to the conduct of clinical trials. * Current in-depth knowledge of regulations governing clinical research, ICH/GCP Guidelines and applicable regulations. * Strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines. * Ability to work, understand and follow work processes within the assigned function. * Strong analytical and conceptual capabilities, interpersonal skills, and ability to communicate with clarity. * Ability to address study related clinical site issues with appropriate guidance and initiates and communicate corrective action as indicated. * Ability to use functional expertise and exercise good judgment. * Demonstrated business ethics and integrity. Flexibility and Availability: In line with Australia’s 'Right to Disconnect' legislation, we recognize and respect employees' right to refuse contact outside of their working hours, unless such refusal is deemed unreasonable. As we operate in an international, matrixed environment, there may be occasions where your role requires participation in business meetings outside of standard hours. We value and support flexibility and appreciate your willingness to occasionally accommodate these requests to ensure effective collaboration and communication within our global team. Additional Information AbbVie is an equal opportunity employer, and dedicated to fostering an inclusive, flexible, and supportive workplace that values and respects every individual. We are committed to operating with integrity, driving innovation, transforming lives, and embracing diversity and inclusion. It is AbbVie’s policy to employ qualified persons of the greatest ability. We ensure a fair and inclusive recruitment process without discrimination against any employee or applicant because of, and not limited to, race, religion, age, physical or mental disability, gender identity or expression, sexual orientation, or marital status. Our hiring process is flexible and accessible, so if you have any specific requests or accessibility requirement, please feel comfortable to let our team know by emailing CareersANZ@abbvie.com or speaking with your Recruiter and we'll make any necessary adjustments to accommodate your needs. WAYS WE WORK All For One Abbvie; We weigh all decisions against the common good. We inspire, share and create as a team. We solve problems for all rather than serving our immediate team. * Decide Smart \& Sure; We make intelligent decisions to create the best outcomes. We act quickly, embrace experimentation, and learn what doesn’t work and get on to what does. * Agile \& Accountable; We streamline and eliminate unnecessary obstacles. We plan but adapt as we go. We delegate and make tough decisions to ensure focus on results, staying keenly aware of the urgency in all we do. * Clear \& Courageous; Open, honest, candid dialogue is core to our work and how we act with each other. We share information freely and continuously to find solutions. We admit mistakes. We grow stronger by putting the courage of our conviction to the test. Make Possibilities Real; We question with endless curiosity. We’re never satisfied with good enough—patients depend on us to deliver more. We challenge ourselves to find creative, constructive solutions to turn possibilities into reality. * CODE OF CONDUCT \& BUSINESS INTEGRITY STATEMENT AbbVie is committed to observing high integrity and ethical standards in all its business dealings with our customers, with each other, business partners and suppliers. * AbbVie as a responsible corporate citizen will adhere to these standards, as well as to local, national and international laws. * All AbbVie employees are responsible for maintaining the Company’s reputation for conduct in accordance with the highest level of business integrity, ethics and compliance with the law. * Soliciting and/or accepting/attempting/offering bribes or any illegal gratification is therefore cause for immediate dismissal. * AbbVie is committed to operating with integrity, driving innovation, transforming lives, serving our community, and embracing diversity and inclusion. AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. US \& Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html US \& Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.abbvie.com/join-us/reasonable-accommodations.html

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Clinical Research Associate II (FSP)

Thermo Fisher ScientificMelbourne, Victoria, Australia

From $50/yr

Work Schedule Standard (Mon-Fri) Environmental Conditions Office As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer. About the Role: Join Us as a Clinical Research Associate (Level II) – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750 biotech's, spanning 2,700 clinical trials across 100+ countries in the last 5 years. As part of our global team, you’ll have the opportunity to perform and coordinate all aspects of the clinical monitoring and site management process. As a Clinical Research Associate (Level II), you'll conduct remote or on-site visits to assess protocol and regulatory compliance and manage required documentation. What You'll Do: * Monitors investigator sites with a risk-based monitoring approach: applies root cause analysis (RCA), critical thinking and problem-solving skills to identify site processes failure and corrective/preventive actions to bring the site into compliance and decrease risks. * Ensures data accuracy through SDR, SDV and CRF review as applicable through on-site and remote monitoring activities. Assess investigational product through physical inventory and records review. Documents observations in reports and letters in a timely manner using approved business writing standards. * Escalates observed deficiencies and issues to clinical management expeditiously and follow all issues through to resolution. May need to maintain regular contact between monitoring visits with investigative sites to confirm that the protocol is being followed, that previously identified issues are being resolved and that the data is being recorded in a timely manner. * Conducts monitoring tasks in accordance with the approved monitoring plan. Participates in the investigator payment process. * Ensures a shared responsibility with other project team members on issues/findings resolution. Investigates and follows-up on findings as applicable. * Participates in investigator meetings as necessary. * Identifies potential investigators in collaboration with the client company to ensure the acceptability of qualified investigative sites. Initiates clinical trial sites according to the relevant procedures to ensure compliance with the protocol and regulatory and ICH GCP obligations, making recommendations where warranted. * Performs trial close out and retrieval of trial materials. * Ensures that required essential documents are complete and in place, according to ICH-GCP and applicable regulations. * Conducts on-site file reviews as per project specifications. * Provides trial status tracking and progress update reports to the Clinical Team Manager (CTM) as required. * Ensures study systems are updated per agreed study conventions (e.g. Clinical Trial Management System). * Facilitates effective communication between investigative sites, the client company and the PPD project team through written, oral and/or electronic contacts. * Responds to company, client and applicable regulatory requirements/audits/inspections. * Maintains \& completes administrative tasks such as expense reports and timesheets in a timely manner. * Contributes to the project team by assisting in preparation of project publications/tools, and sharing ideas/suggestions with team members. * Contributes to other project work and initiatives for process improvement, as required. Education * Bachelor's degree in a life sciences related field or a Registered Nursing certification or equivalent and relevant formal academic / vocational qualification. * Valid driver's license where applicable. Experience * Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 1 years as a clinical research monitor) or completion of PPD Drug Development Fellowship. * In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role. Knowledge, Skills, Abilities * Proven clinical monitoring skills * Demonstrated understanding of medical/therapeutic area knowledge and medical terminology\ * Demonstrated ability to attain and maintain a working knowledge of ICH GCPs, applicable regulations and procedural documents * Well-developed critical thinking skills, including but not limited to: critical mindset, in-depth investigation for appropriate root cause analysis and problem solving * Ability to manage Risk Based Monitoring concepts and processes * Good oral and written communication skills, with the ability to communicate effectively with medical personnel * Ability to maintain customer focus through the utilization of good listening skills, attention to detail and the ability to perceive customers’ underlying issues * Good organizational and time management skills * Effective interpersonal skills * Attention to detail * Ability to remain flexible and adaptable in a wide range of scenarios * Ability to work in a team or independently as required Benefits Join our team and take advantage of these great benefits! Apply now to learn more about the full range of benefits we offer. * Health \& Wellbeing: Join a company that prioritizes your health \& wellbeing with comprehensive benefits, wellness programs, and an Employee Assistance Program providing confidential support for personal and work-related issues. * Flexibility: Balance your work and personal life with flexible arrangements. * Extra Leave: Benefit from generous leave policies, including the option to purchase additional leave, paid birthday leave, and company paid parental leave. * Charitable Giving \& Volunteering: Make an impact with paid volunteer time to support non-profit organizations that matter to you. * Learning \& Development: Advance your career with access to online courses via Thermo Fisher Scientific University Plus and LinkedIn learning, workshops, and mentorship programs for continuous learning and skill development. Thermo Fisher Scientific Australia WGEA Employer of Choice for Gender Equality Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 125,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory at Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued. Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

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Clinical Research Associate

NovoPuteaux, A8, FR

From $49/yr

Category: Clinical Development Location: Puteaux, Île-de-France, FR Department: Operations Excellence \& Study Start-up, Clinical Development Centre France, International Operations Location: Paris, France, with travel to clinical trial sites if required Job category: Clinical Development Your impact begins here As Clinical Research Associate, you will be the link between Novo, clinical trial sites and study teams in France. You will make sure trials run to protocol, data can be trusted and the safety and rights of every trial participant are protected. Using risk-based monitoring, you will spot issues early and help sites deliver on time and to high quality. Your work helps move new treatments closer to the people living with serious chronic diseases who need them. What you’ll bring You know how to run high-quality trials at site level, and you build the kind of relationships that keep studies moving. You will also bring: * A bachelor’s degree in Life Sciences or a related field. * 1+ years’ experience in clinical trial monitoring, or in a relevant pharmaceutical industry or CRO role. * Strong knowledge of ICH-GCP guidelines, regulatory requirements and clinical trial methodology, and a track record of compliant, high-quality trial execution. * Strong organisational, time management and project management skills, with the ability to manage multiple sites and priorities with close attention to detail. * Confidence using digital trial tools, including EDC systems, CTMS and eTMF. * Excellent written and verbal communication, and the ability to build trusted relationships with internal and external stakeholders at all levels. * A proactive approach to problem-solving, risk identification and decision-making, working both independently and as part of a team. * Flexibility to travel to sites as required. * Fluency in French and professional English. Useful, but not essential: * Hands-on experience applying risk-based quality management (RBQM) principles in study conduct. * Experience supporting audits or regulatory inspections. What you’ll do You will oversee your assigned trial sites from monitoring through to inspection readiness, making sure every study delivers reliable data while protecting the people taking part. * Act as the primary liaison between Novo, clinical sites and cross-functional study teams, building strong relationships with investigators and site staff. * Conduct on-site and remote monitoring visits in line with the Monitoring Plan, Protocol, ICH-GCP, internal SOPs and regulatory requirements. * Protect patient safety and data integrity by reviewing site data, resolving discrepancies, managing adverse events and keeping data cleaning on track. * Track site performance, recruitment and retention, and resolve site-level issues early to keep timelines and quality on target. * Apply RBQM principles to identify, assess and reduce risks, maintain inspection readiness and support audits and inspections. * Train and support sites on protocols, procedures and systems, and manage investigational medicinal product, study supplies, essential documents and the Investigator Trial Master File. * Share site feedback and insights to improve protocols, patient engagement and operational planning. Who you’ll work with You will join the Operations Excellence \& Study Start-up team at the Clinical Development Centre in France, part of International Operations, and report to a Clinical Operations Manager. Day to day, you will work closely with investigators, study nurses, coordinators and pharmacists at your sites, as well as key opinion leaders and vendors. Inside Novo, your closest partners will be Trial Managers, the Study Start-up team, Vendor Managers, trial squads and the Global Project Team, alongside Clinical Operations, Medical Affairs and country management teams. You will sit at the point where global trial plans meet real sites and real people. By keeping communication clear and raising issues early, you help everyone move with speed and confidence. What you can expect here You will be trusted to own your sites and make decisions that keep studies on track, supported by colleagues across clinical operations. Your insights from the field will be heard and can shape how trials are planned and run. You will build your skills through investigator meetings, CRA training sessions and work on a range of trials, and you will be encouraged to explore new technologies and digital tools that improve how we work. Clear performance expectations help you deliver your best work and be recognised for it. Salary For this role, the Annual Base Salary ranges from 49.200 Euros to 71.340 Euros corresponding to the level of the position. The placement within the salary range will be assessed during the recruitment process based on the candidate's skills, competencies, knowledge, and relevant experience. Incentives and Benefits The salary package may include short-term and/or long-term incentives as well as other employee benefits based on position level, location, functional area and relevant market benchmarks. Start now Your impact begins today. If you are ready to help bring high-quality clinical trials to life in France, apply for the Clinical Research Associate role by 23 October 2026. Applications are reviewed on an ongoing basis, so we encourage you to apply as soon as possible.

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Companies hiring for Clinical Research Associate

ClinoGenesis Research Institute (1)Emerald Clinical (1)AbbVie (1)Thermo Fisher Scientific (1)Novo (1)

Clinical Research Associate Salary Data

View detailed salary ranges from 5 listings with reported compensation ›

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