Medical Monitor at ClinChoice

Aachen, North Rhine-Westphalia, Germany -

Full Time

Start Date

Immediate

Expiry Date

09 Feb, 26

Salary

0.0

Posted On

11 Nov, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Support, Medical Advice, Data Analysis, Protocol Writing, Training, Recruitment, Retention, Medical Queries, Clinical Trials, Microsoft Office, Fluent English, Medical Interpretation, Investigator Meetings, On-call Coverage, Study Data Review, Therapeutic Area Knowledge

Industry

Pharmaceutical Manufacturing

Description

ClinChoice is a global full-service CRO dedicated to professional development and providing an excellent work-life balance, with a quality-focused, collaborative “one-team” culture. We are looking for a dynamic person to join our in-house team as a Medical Monitor on a permanent basis. This is a hybrid position, to be based either in Italy, Poland, Spain, Germany, Netherlands, Belgium, United Kingdom. The Medical Monitor will provide clinical support to the Clinical Operations team from study design through to dissemination of the results. Join our team: you can be part of making a difference in peoples’ lives and experience a fulfilling and rewarding career! Main Job Tasks and Responsibilities: Will be the Clinical Advisor for the entire lifecycle of the clinical trial by answering medical questions. Participates in the project meetings by giving medical advice. Reviews study data listing from a medical point of view. Analyzes and makes an independent interpretation of study data/results. Writes and reviews protocol, Case Report Forms (CRF) and Clinical Study Reports (CSR). Provides training in specific disease/therapeutic area. May provide study team with assistance in developing criteria for investigator site selection and networking for potential investigators for study participation. Participates in subject recruitment and retention activities which may include per sponsor request individual calls to Key Opinion Leaders, Investigators and site staff, and participation in teleconference and virtual presentations. May present protocol and safety reporting information at Investigator Meetings (as required). Provides on-call coverage for medical queries on the protocol. Education, Experience and Skills University Degree in medical disciplines. At least two (2) years of medical experience Previous experience or knowledge of the clinical trial process. Fluent in English and local language(s). Proficiency in Microsoft Office (e.g. Word, Excel, Outlook). Willingness to travel. The Application Process Once you have submitted your CV, you will receive an acknowledgement that we received it. If you have the requirements we need, you will be invited for phone interview as the first step. Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful. Who will you be working for? About ClinChoice ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. We have over 28 years of proven high-quality delivery and results across all our services with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific. We are on a mission to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Join our passionate team and make a meaningful impact on global healthcare! Our Company Ethos Our mission drives our culture: to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Our employees are the most valuable company asset and they are the fulcrum around which all ClinChoice activities are built and close management and training is the core instrument to develop and maintain highly-qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives to all personnel the clear tools needed to manage both internal and client processes with the same methodology. The success of these core values is evidenced by our below industry average turnover rates. ClinChoice is an equal opportunity employer. We have based our success on attracting, developing, and promoting talent guided by diversity and inclusivity. Our employees come from very diverse backgrounds: gender, race, beliefs, and ethnicities. We recognize this is our strength and celebrate it. Key words: Medical Monitor, Clinical Research Physician, Medical Doctor, MD, CRO, Contract Research Organisation. #LI-CM1 #LI-FULLTIME

Responsibilities

The Medical Monitor will provide clinical support to the Clinical Operations team throughout the clinical trial lifecycle. Responsibilities include answering medical questions, reviewing study data, writing protocols, and providing training in specific disease areas.