3711 Clinical Research Jobs - Page 47

About The Role Skill required: Regulatory Services - Life Sciences Regulatory Operations Designation: LifeScience Regulatory Svs Analyst Qualifications: Master of Pharmacy Years of Experience: 3 to 5 years What would you do? You will be aligned with our Life Sciences R&D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions. Employees under this span will be a part of one of the sub-offerings - Clinical, Pharmacovigilance & Regulatory, helping the worlds leading biopharma companies bring their vision to life enabling them to improve outcomes by c...

About The Role Skill required: KYC Screening - Know Your Customer (KYC) Designation: Regulatory Compliance Senior Analyst Qualifications: Any Graduation Years of Experience: 5 to 8 years What would you do? Help clients transform their compliance function from reactive to proactive through an intelligent compliance operating model powered by data, intelligent technologies and talentLooking for someone with AML and Fraud mgmt experience.Understand & implement laws, and regulations designed to stop the practice of generating income through illegal actions during transfer of funds. Anti Money Laundering law covers limited number of transactions and criminal behaviors to prevent terrorist financi...

Responsibilities: Develop and maintain strong relationships with KOLs, academic institutions, medical societies, and other relevant stakeholders in assigned therapeutic areas. Serve as a credible and trusted scientific resource for healthcare professionals, providing accurate and up-to-date information on our products, disease states, clinical data, and treatment guidelines. Identify and engage with potential investigators for company-sponsored clinical trials and support investigator-initiated research studies (IIS) by providing scientific and logistical support. Deliver scientific presentations and educational programs to HCPs, both individually and in group settings, to enhance understand...

We are looking for a highly skilled and experienced Analyst to join our team in the IT Services & Consulting industry. The ideal candidate will have 6-8 years of experience in KYC analysis. Roles and Responsibility Conduct thorough analysis of customer data to identify potential risks and ensure compliance with regulatory requirements. Develop and implement effective risk management strategies to mitigate identified risks. Collaborate with cross-functional teams to resolve complex issues and improve overall process efficiency. Provide expert guidance on KYC procedures and best practices to junior team members. Stay up-to-date with changes in regulations and industry standards related to KYC....

OVERALL PURPOSE OF THE ROLE: The Line Manager Is responsable to support the Operations Manager to deliver the service demandes of the DEPOT by leading and facilitating effective team working among the team members for servicing / planned maintennece and renovation/modernisation/corrective maintenance activity. The purpose of the job is to Manage all the maintenance activities (PM/ CM/ A&V) in the Line/Workshop including the responsibilities linked to the position as hierarchical manager of the employees of the Maintenance organization who belong to this Line/Workshop RESPONSIBILITIES: Team Management Lead all aspects of the team in the maintenance, servicing to meet customer requirements wit...

We are looking for a skilled Associate Process Manager to join our team at eClerx Services Ltd., responsible for managing the KYC process. The ideal candidate will have a strong background in IT Services & Consulting, with excellent leadership and management skills. Roles and Responsibility Manage and oversee the KYC process to ensure compliance with regulatory requirements. Develop and implement process improvements to increase efficiency and reduce costs. Collaborate with cross-functional teams to identify and mitigate risks. Analyze data and metrics to optimize processes and improve customer satisfaction. Train and guide team members on new processes and procedures. Monitor and report on ...

We are looking for a highly skilled and experienced Analyst to join our team in the IT Services & Consulting industry. The ideal candidate will have 6-9 years of experience in KYC analysis. Roles and Responsibility Conduct thorough analysis of customer data to identify potential risks and ensure compliance with regulatory requirements. Develop and implement effective risk management strategies to mitigate identified risks. Collaborate with cross-functional teams to resolve complex issues and improve overall process efficiency. Provide expert guidance on KYC procedures and best practices to junior team members. Stay up-to-date with industry trends and regulatory changes to ensure the organiza...

We are looking for a skilled Associate Process Manager to join our team at eClerx Services Ltd., responsible for managing the Know Your Customer (KYC) process. The ideal candidate will have a strong background in IT Services & Consulting, with excellent analytical and problem-solving skills. Roles and Responsibility Manage and oversee the KYC process to ensure compliance with regulatory requirements. Develop and implement process improvements to increase efficiency and reduce errors. Collaborate with cross-functional teams to resolve issues and enhance customer experience. Analyze data and metrics to identify trends and areas for improvement. Implement risk management strategies to mitigate ...

Residential Medical Officer (RMO) will provide 24x7 medical care, emergency handling, and patient monitoring in a rural hospital. Must reside on campus, support consultants, ensure records, and maintain protocols for safe, quality care. Required Candidate profile MBBS/ BAMS/ BHMS/ BAMS/ BUMS with valid registration, 0–3 years’ experience (freshers welcome), strong clinical and emergency skills, good communication, willing to work in rural healthcare setup. Perks and benefits Accomodation

You will be playing a key role in developing clinical database products across various therapeutic areas such as Metabolic & CV, Neuroscience, Autoimmune, Oncology, and Respiratory with a focus on high quality to support Meta-analysis. Your responsibilities will include analyzing and annotating trial design information, treatments, demographics, and outcomes data from clinical literature sources. You will also be required to digitize results from graphs accurately and consistently. Collaboration will be a key aspect of your role as you work with lead consultants, peer data analysts, and quality managers to contribute to database rules, specifications, and quality processes. Additionally, you...

As a Pharmacovigilance/Senior Pharmacovigilance Associate at ICON plc, you will play a crucial role in reviewing and processing safety events, including pre-marketing, post-marketing, medical device, and drug-related information. You will be responsible for conducting safety reviews of clinical and diagnostic data, generating data listings from the safety database, and ensuring the accuracy and quality of the data. Additionally, you will support the development of safety management plans, post-marketing safety activities, and participate in safety-related meetings and teleconferences. Your key responsibilities will include collaborating with cross-functional teams to support safety-related i...

As a qualified candidate for the position, you should hold a DM/DNB in Pediatric Hematology, Pediatric Oncology, or Pediatric Hemato-Oncology from an institute recognized by the National Medical Commission (NMC). Your experience should align with the norms set by NMC and affiliating university for teaching faculty positions. Having teaching experience in a recognized medical college, publications in indexed peer-reviewed journals, and exposure to clinical research and academic program development would be considered additional desirables for this role. Your key responsibilities will include conducting undergraduate and postgraduate teaching as per NMC curriculum, providing clinical care to c...

The Sr. Clinical Research Coordinator position at Shree Clinical Research in Belgaum is a full-time on-site role that involves overseeing clinical trials, managing protocols, and ensuring regulatory compliance. In this role, you will be responsible for obtaining informed consent, coordinating with investigators, sites, and patients, and ensuring the smooth execution of clinical research activities. To qualify for this position, you should have experience in Clinical Research and Clinical Trials, proficiency in handling Informed Consent, knowledge of Protocol and Research methodologies, strong organizational and communication skills, and the ability to work both independently and collaborativ...

The clinical operations activities at our organization are expanding rapidly, and we are currently looking for a full-time Clinical Research (CRA) Manager to join our Clinical Monitoring team in Navi Mumbai, India. In this role, you will play a crucial part in the clinical trial management process at Medpace. If you are seeking a challenging career where you can utilize your existing expertise and further develop and advance your professional journey, then this opportunity is perfect for you. Your responsibilities will include: - Managing a team of Clinical Research Associates (CRAs) - Recruiting, providing initial and ongoing training, and fostering the development of CRAs - Overseeing and ...

The ideal candidate for this role will be responsible for Business Development & Sales tasks such as identifying and targeting potential clients in pharmaceutical, biotech, and medical device companies. You will promote clinical research services offered by the company, prepare and present proposals, budgets, and bids for new projects, negotiate contracts, and close deals to meet company objectives. In addition, you will be involved in Market Research & Strategy by analyzing industry trends, competitors, and client needs to develop growth strategies. Attending industry events, conferences, and networking sessions will be essential to identify leads. You will also develop go-to-market strateg...

You are required to have a professional qualification such as MSc in Life Science, MPharm, BAMS, BHMS, MBBS, along with experience in medical writing. Excellent communication skills and a good understanding of clinical research are essential for this role. Your responsibilities will include preparing and editing medical and scientific manuscripts and abstracts, as well as producing and publishing peer-reviewed scientific papers and presentations that explain the results of clinical studies. You should possess good communication skills and have a thorough understanding of editing and regulatory processes and requirements. If you meet the qualifications for this position and are interested in ...

At Medtronic, you can embark on a lifelong career dedicated to exploration and innovation, all while advocating for healthcare access and equity for all. Your role will be purpose-driven, aimed at breaking down barriers to innovation in a more interconnected and compassionate world. As a Clinical Research Specialist at Medtronic, based in India, your responsibilities will include overseeing, designing, planning, and developing clinical evaluation research studies. You will be involved in preparing and authoring protocols and patient record forms, as well as conducting clinical studies of products that address medical needs or have commercial potential. You will interpret the results of clini...

The Associate Medical Expert in Translational Clinical Oncology (TCO) plays a crucial role as the medical leader for various global studies, roll-over studies, long-term follow-up studies, and studies in the close-out phase. Working under the guidance of a Clinical Program Leader (CPL) and/or Medical Expert, you will provide essential medical support for assigned aspects of active TCO studies. TCO is a department within the Biomedical Research division that focuses on designing and conducting early phase clinical studies in cancer patients, aiming to develop innovative treatments for oncology conditions and bridge the gap between drug discovery and late-phase clinical development. In this ro...

As a Manager of Clinical Research at The Ayurveda Experience, you will be responsible for leading and managing clinical trials and research studies to ensure timely delivery, budget adherence, and compliance with regulatory standards. In this role, you will supervise research teams, collaborate with cross-functional departments, and provide strategic direction to achieve high-quality research outcomes that align with the company's mission. Your responsibilities will include planning, initiating, and overseeing clinical research projects from start to finish while ensuring adherence to protocols, timelines, budgets, and Good Clinical Practice (GCP) standards. You will lead and mentor clinical...

Thepharmadaily LLP is looking for Biostatistician I to join our dynamic team and embark on a rewarding career journey Collect, analyze, and interpret data related to healthcare and clinical research. Develop and apply statistical models to address research questions. Collaborate with researchers to design studies and experiments. Prepare statistical reports and present findings to stakeholders. Ensure the integrity and accuracy of data and statistical analyses. Stay updated with the latest statistical methods and software.

Veranex's mission as an Innovation CRO is to improve patient outcomes by accelerating our clients" innovations to market. As the world's only end-to-end professional services firm focused on MedTech, we take clients" Vision to Velocity through our comprehensive service portfolio, with expertise in human-centered design and product development, preclinical and clinical research, regulatory affairs, and market access and reimbursement consulting. Veranex has an exciting opportunity for you to join our team as a Clinical Data Co-ordinator 2. As a member of the Clinical Data Management team, you will play a vital role in improving lives globally through medical technology innovation and Data Man...

The Group Leader -GCP QA (Clinical) at Syngene in Bangalore is responsible for managing the GCP QA auditors team and conducting various audits related to clinical research, process audits, Investigational Site audits, and safety database audits. The role involves assessing systems and practices to improve the GCP Quality System practices in alignment with the national and international GCP Quality System standards. The Group Leader must ensure compliance with quality (GxP) regulations and standards, making the facility audit-ready at all times. Key Responsibilities include: - Scheduling and conducting GCP QA audits to ensure compliance with regulatory requirements - Developing risk-based aud...

Description We are seeking a dedicated and skilled Para Medical professional to join our healthcare team. The ideal candidate will play a crucial role in providing high-quality patient care and supporting medical staff in various procedures. Responsibilities Assist in patient care and support medical staff in diagnostic and therapeutic procedures. Perform basic medical procedures such as taking vital signs, administering injections, and conducting laboratory tests. Maintain patient records and documentation accurately and ensure confidentiality. Communicate effectively with patients to explain procedures and provide comfort. Assist in the management of medical supplies and equipment, ensurin...

As an experienced medical writer with expertise in CTD medical writing and clinical development of medicines, your responsibilities will include the following: Writing high-quality CTD modules such as nonclinical and clinical overviews & summaries (Module 2.5, 2.4, 2.7, 2.7) to meet EU submission requirements. Addressing clinical deficiencies by providing appropriate responses. Contributing to drug development strategy. Updating documents like SmPC, Patient Information Leaflet, CCDS, Safety variations. Preparing Clinical Study Reports, Study design, and synopsis. Assisting in the formulation of clinical development strategies and reviewing study reports and published papers. Conducting liter...

We are offering a 6-month full-time internship at our organization, aimed at graduates and freshers who are looking to start a long-term career. Upon successful completion of the internship, eligible and high-performing candidates will be offered permanent employment with us. Responsibilities - Work closely with our Clinical Research team - Maintaining accurate documentation and data collection for clinical trials - Coordinating clinical research studies - Maintain reports and update internal systems regularly - Participate in team meetings, training sessions, and project briefings - Assist in day-to-day project tasks and documentation Requirements - Bachelor's degree in a related field (e.g...