Director, Clinical Affairs

ClinicalPro is seeking a Director, Clinical Affairs for a leading Medical Devices organisation located in the USA.

This individual will be responsible for advancing strategic clinical objectives and directing the execution of many clinical research programmes, managing clinical operations, and leading scientific teams.

Must be eligible to work in the USA.

Responsibilities

• Implement the Clinical Affairs policies and procedures in accordance with the pertinent business goals.
• Establish and maintain professional connections with physicians, professional associations, key opinion leaders (KOLs), scientists, and other parties pertinent to Clinical Affairs initiatives.
• By offering advice and information from the scientific community, assist KOL development.
• Overseeing the creation of the content for scientific papers, manuscripts, and abstracts; offering cross-functional assistance in examining materials for correctness in science and conformity to pertinent standards and procedures.
• At gatherings or functions, present pertinent scientific knowledge.
• To comprehend the context and spot any potential contradictions in the data, do a survey of the literature, abstracts, podium presentations, and scientific paper publications.
• To guide the development of future programmes, review pertinent literature, and analyse clinical and research data.
• Actively assess competing clinical and scientific evidence to protect important intellectual property.
• Assist the clinical team in analysing data, developing data reviews, drawing inferences from the data, and creating clinical reports.
• Support regulatory submissions revising portions of documentation.
• Give advice about the veracity of the clinical and scientific information in advertising.
• Recognise business requirements and cultivate credibility and goodwill among colleagues.
• Participate in the collaborative effort by doing pertinent tasks as needed.
• Respect the rules, regulations, and job directions.

Skills and Requirement

• Ph.D. or an MSc in biomedical engineering or a closely related field.
• Ten or more years experience working in a highly regulated field.
• Travel (10–20%).
• It is desirable if you have knowledge of active implanted medical device technologies.
• shown writing and presenting abilities in science.
• Past oral podium presentations and peer-reviewed publications.
• Knowledge of software in devices, data analytics, data visualisations, data collecting, and data management. Advanced software application abilities.

Apply

If you’re interested in this position, apply now to send us an updated copy of your CV, or give us a call right away.

---

To explore more opportunities, visit Opportunities at ClinicalPro