1999 Clinical Trials Jobs - Page 10

Define major accountabilities and/or activities. List most complex or difficult parts of job first and indicate percentage of time required to perform each task. Key roles may be different country by country. So, % of time can be put at each OpCo level considering local situation. TA Leadership New Product Launches Be trusted scientific experts in the related TA -New Product Launches Be aware of latest scientific and clinical advances in relevant therapy areas. Know well and skillful in conducting literature search and good ability in reading and analyzing clinical papers to promote evidence/scientific-based brand concepts. Provide regular clinical & scientific knowledge sharing across the T...

About the Role: Grade Level (for internal use): 07 The Team : The team is responsible for developing, maintaining, and enhancing drug database products, delivering strategic and financial insights to clients, and creating innovative, client-facing functionalities. The team values collaboration, precision, and a forward-thinking approach to driving impact in the healthcare data landscape. The Impact : This role contributes directly to the creation and management of high-quality drug databases, supporting critical decision-making in the healthcare and biopharma sectors. By providing contextual information on drugs and ensuring the accuracy and usability of drug data, this position enhances the...

Join Clario in transforming how clinical trials are delivered globally. As a Clinical Systems Translations Project Manager, you ll play a pivotal role in ensuring our electronic solutions are linguistically validated and regulatory-ready across diverse global studies. This is a client-facing role with high visibility and impact ideal for someone who thrives in cross-functional environments and is passionate about quality and precision. What We Offer Competitive compensation Attractive benefits (security, flexibility, support and well-being) Engaging employee programs Technology for hybrid working and great onsite facilities What Youll Be Doing Own and manage all translation-related tasks for...

Career Category Research Job Description Manager Competitive Intelligence R&D , CD&A Role Name: Manager of Competitive Intelligence R&D, CD&A Department Name: Customer Data and Analytics (CD&A) Role GCF: 5 ABOUT AMGEN Amgen is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing, and delivering innovative human therapeutics. This approach begins by using tools like advanced human genetics to unravel the complexities of disease and understand the fundamentals of human biology. A biotechnology pioneer since 1980, Amgen has grown to be one of the world s leading independent biotechnology companies, reaching milli...

Dear Candidate, CBCC Global Research is looking for CRA/Sr. CRA with onco PK experience for Pune location. Job Code : CBCC/IND/CRA (Please mentioned job code in subject line of your application ) Work Experience: 3-8 Years Monitoring experience with Oncology PK studies is mandatory Work Location: Pune Pre-Requisite Skills: Minimum 2 years onsite monitoring experience mandatory Patient base PK studies monitoring experience is preferred Key Responsibilities Overall site management of clinical trials and Patient base PK studies Ensure effective communication to sites Prepare for site visits Assist PM in developing the project plan Prepare the Site Activation checklist Handle back-office monitor...

Career Category Research Job Description Senior Manager Competitive Intelligence R&D , CD&A Role Name: Sr Manager of Competitive Intelligence R&D, CD&A Department Name: Customer Data and Analytics (CD&A) Role GCF: 6 ABOUT AMGEN Amgen is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing, and delivering innovative human therapeutics. This approach begins by using tools like advanced human genetics to unravel the complexities of disease and understand the fundamentals of human biology. A biotechnology pioneer since 1980, Amgen has grown to be one of the world s leading independent biotechnology companies, reac...

Dear Candidate, Below are the Job Details for Clinical SAS Programmer role at CBCC Global Research LLP. Candidate should have the exposure of SDTM, ADAM and TLF. Job Location : Ahmedabad At Office Position : 2 Experience: 2-5 years in CRO preferred / Pharma industry Qualification : M. Sc. Statistics/Any Science Graduate Mandatory experience in Clinical trials Responsibilities: Ensure consistently high quality outputs for reporting and submission- 1.1. Build SAS datasets from clinical database. 1.2. Develop SAS macros, templates and utilities for data cleaning and reporting. 1.3. Utilize SDTM guidelines to build datasets. 1.4. Communicate with an internal team to create deliverables for pharm...

Responsibilities: Assist in designing business collaterals, including presentations, reports, and promotional materials. Create visual content for events, such as flyers, posters, banners, and social media posts. Develop business videos, mailers, and digital assets to support marketing campaigns. Support the execution of design projects from conceptualization to completion. Collaborate with other teams to understand project requirements and provide design solutions. Maintain high-quality standards and consistency in design across all materials. Contribute to the overall creative process and offer suggestions to improve design and layout. What are we looking for? Bachelors or Masters degree i...

Clin Infotech is Offering Internship Opportunity For Freshers to gain Work Experience on Live Projects and Clinical Software's in Clinical Research and Pharmacovigilance Internship Is followed with Certification Course in Clinical Research. Required Candidate profile Should be pharmacy & Life Science Graduates Should have done Certification Course in Clinical Research and Pharmacovigilance Diploma in Clinical Research will be Preferable Good Communication Skills Perks and benefits Please apply through Naukri.com only.

Study Coordination: Manage and oversee all aspects of clinical research studies, till the closeout. Participant Recruitment: Screen and recruit study participants Data Management: Collect, record, and maintain accurate study data and documentation. Required Candidate profile Knowledge of the pharmaceutical industry, terminology, and practices. - Knowledge of FDA regulations and their practical implementation. - Strong verbal and written communication skills.

Urgent Clin Infotech Hiring B.Pharm Freshers With Certification in Clinical Research and Clinical Data Management Candidate With Hands On Experience In Clinical Data Management Is Preferrable Required Candidate profile Candidate With Knowledge in Clinical Research Roles and Responsibilities is Prefferable Candidate Should have Good Communication Skills is Mandatory

Should have knowledge in clinical research studies Monitoring of Clinical studies conducted at various CROs located globally as per ICH/GCP, applicable regulatory requirements, protocols and SOPs. Perform Site visits (i.e. Site Selection Visit) Required Candidate profile Strong understanding of clinical trial processes and regulatory requirements. Excellent clinical assessment skills and a commitment to patient safety and ethical research practices.

Clin Infotech is offering internship Opportunities for B.Pharm and M.Pharm Freshers who are willing to start a career in Clinical Research Pharmacovigilance clinical data management sas Medical writing and Medical coding Required Candidate profile Clinical Research Internship includes of Hands on Experience on softwares in Clinical Research Pharmacovigilance clinical data management Domain. B.Pharm M.Pharm and Pharm D Are Eligible to Apply

Coordinate and manage clinical trials from initiation to completion, ensuring compliance with regulatory guidelines and study protocols Recruit, screen, and enroll study participants while maintaining accurate documentation and records Required Candidate profile Maintain study supplies, track data collection, and support data analysis, ensuring high-quality and ethical research practices throughout the study

JD: Skills : CDM- clinical data management,PV- pharmacovigilance ,statistical Data,Discrepancy management- Domain- Life science,Clinical trial design -Leading training teams Good to have : SAS,statistical programming Exp : End to end CDM exp||TL exp for 15-20 PPL US UK shift- should be flexible - WFO What are we looking for? •Commitment to quality • Education Graduate from an accredited college or university; or an equivalent level of education. • 12-16 years of experience, with at least 6-8 years in end-to-end clinical data management and Pharmacovigilance and 4-6 years of training experience on process/language/soft skills • Prior experience in managing teams directly and indirectly. • Exc...

Job Title: Business Analyst Market Access & Pricing Software Location: Hyderabad, India (flexible working arrangements) About Us Access Infinity is a fast-growing Pharma tech company revolutionizing how pharmaceutical companies approach global market access and pricing strategy. Our leadership team brings over five decades of experience in the highest levels of Market Access and Pricing. We offer a dynamic environment focused on innovation, learning, and delivering real-world value to our clients. With 20+ structured learning modules, we invest heavily in subject matter training and core skill development to support your growth. Our accessible leadership team, flat structure, and commitment ...

You are an experienced project management professional with a proven ability to lead complex, cross-functional projects in a dynamic environment. Your expertise lies in managing projects that ensure the timely execution of R&D, clinical trials, and product launches. Your strategic oversight, strong collaboration across departments, and ability to deliver results in a fast-paced environment are key drivers of success. You will oversee the entire lifecycle of projects, from initiation through launch, ensuring alignment with business goals. Leading cross-functional teams, coordinating with R&D, manufacturing, regulatory, clinical, and BD teams to drive project milestones. Ensure clinical trials...

As a Manager of Clinical Research at MultiCare, you will play a crucial role in ensuring the efficient and effective implementation of research protocols, starting from protocol development to long-term follow-up. Your responsibilities will include providing project management for multiple complex clinical projects, developing and managing timelines, ensuring quality performance in clinical research, communicating effectively with diverse stakeholders, generating training and study-specific materials, establishing new clinical research sites for rigorous trials, contributing to the growth of the clinical trial business, strategizing to enhance rapid subject recruitment, and promoting departm...

The Head Clinical Operations & Clinical Strategy role in Bangalore requires a highly skilled and independent professional with expertise in clinical research. This individual will be responsible for supporting Global Research & Development activities related to clinical trials by providing excellent data interpretation, creative thinking, and persuasive communication. Working closely with the senior leadership team of R&D, the role involves determining clinical strategies for various products and markets within the global portfolio. Additionally, this position plays a key role in evaluating external partnership opportunities through due diligence assessments. Responsibilities include oversee...

As a Statistical Programmer II at Advanced Clinical, you will play a crucial role in providing programming support for clinical trials. Your responsibilities will include exceeding the expectations and responsibilities of a Statistical Programmer I, understanding and implementing CDISC and other regulatory standards, and following internal SAS programming conventions. You may also serve as a programming lead, prepare programming specifications for SDTM, ADaM, and other derived datasets, and work with cross-functional team members to ensure accurate and high-quality statistical outputs. In this role, you will apply your knowledge of SAS programming to program and develop statistical outputs a...

Job Description As an Executive at Amneal Pharmaceuticals Pvt. Ltd., located in Ahmedabad, you will be responsible for daily tasks related to the Amneal pharmaceuticals complex injectable (Microspheres) division. This full-time on-site role requires a strong background in Medicine and Medical Affairs skills, Research and Clinical Trials experience, as well as Regulatory Affairs knowledge. To excel in this role, you must possess excellent analytical and problem-solving skills, along with attention to detail and strong organizational abilities. Collaboration is key, so the ability to work effectively in a team setting is essential. Previous experience in the pharmaceutical industry is preferre...

Tracom Stock Brokers is looking for Compliance Professional to join our dynamic team and embark on a rewarding career journey Regulatory Compliance: Monitor and ensure compliance with all relevant laws, regulations, and industry standards that affect the organization Policy Development: Develop, implement, and maintain compliance policies, procedures, and programs to mitigate risks and maintain adherence to regulations Risk Assessment:Risk Analysis: Conduct risk assessments and analyze potential compliance risks, providing recommendations for risk mitigation Training and Education:Training Programs: Develop and deliver compliance training programs for employees to ensure awareness and unders...

Drug Safety Physician We are currently seeking a Drug Safety Physician to join our diverse and dynamic team. As a Drug Safety Physician at ICON, you will play a pivotal role in overseeing the medical aspects of pharmacovigilance activities, ensuring the safety of investigational drugs and contributing to the advancement of inNvative treatments and therapies. What you will be doing Review of coding (e.g. MedDRA) and accurate assessment (seriousness, expectedness, listedness, relatedness) of Adverse Events (serious and non-serious) and of Adverse Drug Reactions (serious and non-serious) Provide support to the Drug Information & Pharmacovigilance Product Support (call) Centre and the related pr...

. Our most valuable asset is our people . At ZS we honor the visible and invisible elements of our identities, personal experiences and belief systems the ones that comprise us as individuals, shape who we are and make us unique. We believe your personal interests, identities, and desire to learn are part of your success here. Learn more about our diversity, equity, and inclusion efforts and the networks ZS supports to assist our ZSers in cultivating community spaces, obtaining the resources they need to thrive, and sharing the What You ll Do - You will design & implement various innovative solutions in the realms of clinical trial, data management, analytics You will work in designing commo...

Job Title: Study Start-up and Regulatory Submission Manager Location: Navi Mumbai, India Experience Required: 5 10 years Employment Type: Full-Time Working Days: 2nd & 4th Saturdays; All Sundays Off Job Description We are seeking an experienced Study Start-up and Regulatory Submission Manager to join our clinical operations team in Navi Mumbai. The ideal candidate should have strong expertise in India-specific clinical trial operations , with proven experience managing regulatory submissions and study start-up activities . Key Responsibilities: Lead and manage Clinical Trial Applications (CTA) and regulatory submissions in compliance with Indian regulatory requirements. Drive clinical study ...