Nursing

Career for Drug Safety Associates at Bioclinica - M.Pharm, M.Sc, B.Pharm | Fresher can apply

Bioclinica is a global life sciences solution provider of Pharmacovigilance, Regulatory Affairs, Cardiac Safety, Molecular Marker Laboratory, Trial Supply Optimization, eHealth Cloud, App Xchange, Clinical Adjudication ,Clinical Trials, Medical Imaging, Clinica Trial Management System (CTMS), Risk-Based Monitoring, Site Network, Electronic Data Capture ( EDC) and Payments & Forecasting.

Post : Drug Safety Associate

Opportunity for Senior Clinical Data Manager at Novo Nordisk

Novo Nordisk is a global healthcare company with 89 years of innovation and leadership in diabetes care. The company also has leading positions within Haemophilia care, growth hormone therapy and hormone replacement therapy. Headquartered in Denmark, Novo Nordisk employs approximately 33,300 employees in 75 countries, and markets its products in more than 190 countries Novo Nordisk’s B shares are listed on NASDAQ OMX Copenhagen (Novo-B).

Post : Senior Clinical Data Manager

Job for Clinical Coding Specialist at IQVIA

IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics and human ingenuity to drive healthcare forward.

Post : Clinical Coding Specialist

Work as Medical Recs Coding Senior Representative at NTT DATA Services

At NTT DATA Services, we know that with the right people on board, anything is possible. The quality, integrity, and commitment of our employees are key factors in our company’s growth, market presence and our ability to help our clients stay a step ahead of the competition. By hiring the best people and helping them grow both professionally and personally, we ensure a bright future for NTT DATA Services and for the people who work here.

Post : MEDICAL RECS CODING & TRANSC. SR. REP

Job for Drug Safety Associates at Bioclinica | M.Pharm, M.Sc, B.Pharm

BIOCLINICA is a global specialty clinical trials services provider delivering expertise and technologies to enhance clinical research, data and analytics . Bioclinica delivers focused service supporting multifaceted technologies such as Medical Imaging, Cardiac safety services, Molecular marker laboratory, Drug Safety and Regulatory solutions, Network of research sites, patient recruitment-retention services, and a post-approval research division. Bioclinica serves more than 400 pharmaceutical, biotechnology, and device organizations - including all of the top 20 - through a network of offices in the U.S., Europe and Asia

Post : Drug Safety Associates

Job for Clinical Research Associate at Rho | USA

Rho is a full-service contract research organization optimally sized to deliver results from clinical research with agility and adaptability. Maximizing profitability, stability, and planned growth has helped provide us with the experience, capacities, and capabilities of a larger organization—all without losing touch with our entrepreneurial passion.  From our headquarters in Chapel Hill, North Carolina, we employ more than 400 creative and critical thinkers. We provide excellent service to some of the nation’s leading pharmaceutical, biotechnology, and medical device companies as well as a number of federal agencies. Our experienced teams help our clients bring new products to the marketplace in a wide range of therapeutic areas.

Post : Clinical Research Associate II

Vacancy for Clinical Research Analyst at Duke Nurses | Durham

Duke Nurses are transforming the future of patient care. Guided by our mission, vision and values, we are committed to excellence. We are leaders, innovators, and educators. We are passionate about what we do. Duke University Health System Nursing is committed to quality care of our patients, their family members, and the community through excellence in leadership, practice, innovation, and education.

Coordinate DOCR’s portion of the Clinical Research Institutional Approval process. Review study documents to complete required start-up build in OnCore and meet with study teams to review the billing grid prior to the study orders and Beacon builds for Maestro Care. Collaborate with teams internal and external to DOCR to assess study readiness prior to go-live. Provide clinical guidance and training to Clinical Research Analysts regarding protocol interpretation and billing grid creation.

Post : CLINICAL RESEARCH ANALYST

Job for Quality Manager in NIMHANS at Clinical Development Services Agency | Emoluments upto Rs 80,000/- pm

Clinical Development Services Agency (CDSA) is an extramural unit of Translational Health Science and Technology Institute which is an autonomous institute created by the Department of Biotechnology (DBT), Ministry of Science & Technology, Government of India to strengthen the existing clinical trial / study capacity for affordable health care products in India and raise it to international standards. It is committed to strengthening and expanding the evidence base for healthcare nationally. CDSA has a national reputation for assisting academic investigators, bio-pharma entrepreneurs and innovative SMEs in the delivery of clinical trials and cohort studies throughout their life cycle from set up to closure. Over time, and building on current strengths, the mission of the Clinical Portfolio Section of CDSA is to become a centre of excellence that supports the conduct of Phase III/IV clinical trials and epidemiological studies of national importance.

Post : Quality Manager (ADBS Study)

Career for M.Pharm, B.Pharm, M.Sc as Trainee Medical Coding at GeBBS Healthcare | Fresher apply

GebbsGeBBS is a leading Healthcare outsourcing solutions company based in Englewood Cliffs, New Jersey with a multiple Global Delivery Centers (GDC) located in India. Our in-depth understanding of the Healthcare industry enables us to provide innovative end-to-end Business Process Outsourcing (BPO) solutions to our clients. We help our clients succeed by leveraging on our domain expertise and our innovative and cost effective approach to outsourcing on-shore/ off-shore. GeBBS service and delivery are based on our highly skilled professionals, robust processes, proprietary workflow engines, world-class infrastructure, in-house domain expertise and a commitment to our clients. This combination makes us an ideal partner for your outsourcing needs.

Post : Trainee Medical Coding

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