TRABAJO CLINICAL MEDICAL WRITER BARCELONA, BARCELONA

medical strategy... medical information... medical records... skills: clinical trials... collaborates productively on clinical safety tasks with colleagues from...

We are looking for a medical writer... excellent medical writing skills... the medical writer will support the development and maintenance of global medical information...

As their clinical assets move towards phases i and ii, we are now searching for a clinical development medical director to oversee clinical research and be a key...

Process improvement, training, standard operating procedure (sop) development, other clinical development line function initiatives) may be assigned to lead clinical...

Offer field-based medical support for sobi's clinical research programs, registries, and facilitate the processes related to investigator-initiated research and...

Working relations:  core study team global clinical lead / clinical development lead/ early clinical lead global safety lead data monitoring committee / steering...

Familiarity with complementary tools, including automation & scripting (github, java), and ai/ml tools for documentation (github copilot, chatgpt/openai, writer...

Lead medical assessment for potential new candidates to enter a clinical development phase... participate as medical representative in internal strategic committees...

clinical trial support:  provide technical support for clinical trial activities within the assigned territory, including site authorization and study procedures...

Specific requirements medical doctor... experience in global health and clinical epidemiology research... to support implementation and supervise activities of clinical...

• minimum of 5+ years of experience in clinical research area inclusive of, but not limited to, good clinical practice or good clinical practice quality assurance...

medical evidence practice (mep) our consultants within the  medical evidence practice, support the expansion of patients' access to innovative medicines by strategically...

• organize and participate in medical conferences, seminars, and workshops... •deep understanding of biosimilar products, their regulatory environment, and their...

Support and contribute to medical monitoring of trials...     understanding of scientific and clinical issues related to the design and implementation of clinical...

Support and contribute to medical monitoring of trials... understanding of scientific and clinical issues related to the design and implementation of clinical trials...

clinical development, medical affairs, regulatory affairs)...   demonstrated clinical safety and research expertise in an appropriate disease area...

Selection criteria  medical doctor or registered nurse... together with other referents, s/he will support msf medical activities and programs through close collaboration...