Manager, Clinical Medical - Hyderabad

Join Novo Nordisk as a Clinical Medical Manager and be part of a fast-growing dynamic team where your expertise will shape strategy and execution of Novo Nordisk pipeline in India. · Deliver industry-leading clinical trial excellence with scientific insights and external engageme ...

We are looking for a highly skilled and experienced Clinical Medical Manager to join our team in Hyderabad. The ideal candidate will have a strong background in clinical medicine and excellent leadership skills. · ...

We're changing lives for living. · Deliver industry-leading clinical trial excellence with scientific insights and external engagement · Partner with Clinical Operations Therapy Area Leads and Trial Managers on scientific and medical aspects of early trial planning, start up, rec ...

Join Novo Nordisk as a Clinical Medical Manager and be part of a fast-growing,dynamic team where your expertise will shape strategy and execution of Novo Nordisk pipeline in India. · ...

Are you a skilled medical professional with a passion for Clinical development strategy and a drive to make a real impact? Join Novo Nordisk as a Clinical Medical Manager and be part of a fast-growing, dynamic team where your expertise will shape strategy and execution of Novo No ...

We are seeking a skilled medical professional to join our Clinical Medical team as a Manager. You will spearhead the creation of scientific strategy for clinical trial excellence and translate it into impactful field execution. · ...

Responsible for reviewing adverse event and serious adverse event data in clinical trials for completeness and accuracy. Provides inputs on protocol preparation from a clinical perspective. · ...

The Senior Regulatory Medical Writer-Clinical trials (RMW-CT) is responsible for providing regulatory affairs (RA) strategic document expertise and support to one or more therapeutic areas (TAs) as designated by leadership. · The RMW provides support for the preparation and submi ...

You'll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world. · ...

Clinical medical manager with a passion for clinical development strategy and a drive to make a real impact. Join Novo Nordisk as part of a fast-growing, dynamic team where your expertise will shape strategy and execution of Novo Nordisk pipeline in India. · Deliver industry-lead ...

We are seeking a Clinical Research, CDM, PV, Medical Writing, Biostatistics, Regulatory.The ideal candidate will have experience in Clinical Data Management Jobs, · Clinical Regulatory Writing Jobs, · Clinical Operations Jobs, · Medical Writing Jobs, · Pharmacovigilance (PV) Jobs ...

This is a full-time, on-site role for a Clinic Receptionist in Hyderabad. The responsibilities include managing appointment scheduling and ensuring an efficient check-in process. · Managing appointment scheduling. · Greeting patients and visitors. · ...

Provide comprehensive medical and scientific expertise and oversight for clinical trials, · ensuring study integrity and participant safety. · ...

Serves as a senior medical writer on clinical study or regulatory project teams. Writes edits and coordinates content for clinical/regulatory. ...

The Deputy Medical Superintendent supports the Medical Superintendent in managing medical affairs and supervising clinical services. · MBBS/BAMS/BHMS & MBA/PGDM/MHA · ...

Writing and reviewing clinical/regulatory documents such as clinical trial protocols investigator brochures informed consent forms according to ICH or other guidelines. · CER - Medical Devices or IVD/IVDR (Clinical Evaluation) Module & Documentation writing.Publication manuscript ...

The Medical Director is responsible for overseeing the clinical operations, quality of care, and compliance with medical standards within the organization. · ...

We are seeking an experienced Medical Writer with strong expertise in Medical Devices, In Vitro Diagnostics (IVD), and Software as a Medical Device (SaMD). The ideal candidate will be responsible for developing, reviewing, and maintaining high-quality scientific and regulatory do ...

+As an internal medical / technical / scientific resource, leads medical affairs objectives in the affiliate country. · + · +Minimum 2-3 years post-qualification work experience in Medical affairs function. · Demonstrated ability to learn quickly and convey clinical and non-clini ...

Assist physicians in patient examinations and treatments. Provide emergency support and manage clinical documentation. · ...