Careers
At ClinSearch, we are always interested to hear from job seekers with clinical research, medical writing, or biostatistics and SAS programming experience. At a minimum, our staff members have MS/PharmD/PhD in life sciences and speak French and English.
Fluency in an additional language such as Dutch, German, Swedish, Spanish etc. is beneficial when applying for a CRA job due to the pan-European focus of our monitoring department.
As an employer, ClinSearch is committed to offering:
- Dynamic and truly international work and working environment. We currently have 20 nations represented on the team and most of our projects are international in scope
- Opportunities for continued training and development in areas of company needs and individual interests. Regular training in new regulatory and technological developments
- A flat management structure loosely focused around projects, where everyone can contribute new ideas
- A beautiful, light and airy open office space at the border of Malakoff and Montrouge, with easy access to both Metro lines 4 and 13
- Flexible work hours, with core hours 10-16
- 1 day work from home weekly, confirmed in each individual job offer
- Support with visa requirements for candidates outside the EU, confirmed in each individual job offer
- Team buildings and company events
For ongoing evaluations, please send your CV to
info@clinsearch.net or contact
Bronwyn SECOURGEON to discuss your unique situation: confidentially and in detail.
Specific job offers will be posted when available here and on
our LinkedIn page.
OPEN POSITIONS AS OF JANUARY 2023
Senior Clinical Data Manager, SAS® Programmer (Paris based)
ClinSearch is a European Healthcare Organization which develops innovative solutions and apps in Clinical Research, Patient-Centered Healthcare Systems, Market Access and Public Health.
Responsibilities
The Senior Clinical Data Manager will be responsible for supportive oversight of clinical data management (CDM) activities for assigned programs.
The successful candidate will proactively support the Co-Directors of the Data Department in the execution of clinical evaluations and any other objectives as per corporate strategy and goals.
This position reports to the Co-Directors of the Data Department (Director of Methodology & Statistics and Senior Director of IS/IT).
Your key responsibility is to meet project deliverables in accordance with study milestones/timelines, including data acquisition, quality checking and reporting in compliance with GCP, SOPs and regulatory requirements.
You will oversee the development of study-specific CDM documentation such as eCRF specifications, eCRF completion guidelines, annotated CRFs, edit check specifications, and data management plans - identifying and mitigating risks to data quality, and proper inclusion into the Trial Master File.
You will also be responsible in performing thorough development testing of the eCRF prior to deployment, inclusive of creating UAT Plans, Test Scripts and executing testing as applicable, and in so ensuring completeness, accuracy and consistency of clinical data across all assigned studies.
Other activities include (non-exhaustive list):
- Attendance at internal study team meetings,
- Document query trends and data/query metrics,
- Review data transfer specifications/agreements for consistency with study and program needs,
- Assist the Data Department Managers in implementation of key performance and quality indicators,
- Perform regular tracking and review of key performance indicators,
- Participate in study document reviews, e.g. clinical study protocols, statistical analysis plans, Mock Tables, Figures and Listings shells,
- Review data listings prior to final database locks,
- Contribute to the development of data collection standards in compliance with CDISC, and corresponding standard edit checks and data review listings,
- Participate in the review of, and/or assist with the development of SOPs and working practices.
Qualifications
- Bachelor’s degree or equivalent. Master’s degree in a scientific discipline such as Computer Science, Life Sciences, Statistics, etc. preferred
- Programming and analytical skills using SAS,
- 7 Years of clinical data management experience in the pharmaceutical/CRO industry,
- 7 Years of Electronic Data Capture (EDC) experience,
- Strong knowledge of CDISC (CDASH, SDTM or ADaM), ICH/GCP guidelines, GCP, 21 CFR Part 11, Clinical Data Management best practices,
- Knowledge of R, Python or similar,
- Demonstrated ability to work independently to manage complex projects with multiple priorities,
- Knowledge of general medical coding in the pharmaceutical / biotechnology / Medical Device industries including knowledge of medical dictionaries, coding tools, and coding governance models,
- A high degree of accuracy and attention to detail,
- Excellent verbal and written communication skills.
- English / French bilingual.
ADVANTAGES
- Competitive Salary Package,
- Group Insurance Coverages,
- Flexible work hours with core business hours 10-16h,
- Work from home 2 days/week, rest of the week in the Malakoff office (bordering suburb of Paris on metro line)
- 5 weeks of holidays plus 10 extra days.
THE COMPANY
ClinSearch is a contract research organization providing clinical evaluation services.
Read more about our company: https://www.clinsearch.net and https://www.edclin.com
CONTACT
Bronwyn SECOURGEON bronwyn.secourgeon@clinsearch.net for additional information or to provide your CV.
Scientific Advisor/Epidemiologist-Clinical Trial Methodology/Biostatistics (Paris based)
ClinSearch is a European Healthcare Organization which develops innovative solutions and apps in Clinical Research, Patient-Centered Healthcare Systems, Market Access and Public Health.
The successful candidate will have the opportunity to work with our experienced Scientific Advisors across a portfolio of clinical evaluation projects for our global clients and to hone their expertise in current clinical evaluation, reimbursement and regulatory matters.
The benefits of joining our organization as it develops new service proposals such as MDR consultancy and a digital portfolio are numerous: familiarization with new European legislation, consultancy best practices and the application of scientific methods to real-world industry projects.
DAY TO DAY DUTIES
As Scientific Advisor, you will:
- Apply epidemiological principles and methods to make recommendations regarding the validity of epidemiological data,
- Monitor the scientific and methodological information published in the medical press or presented in scientific congresses,
- Design or evaluate study proposals,
- Evaluate and interpret existing data from literature,
- Prepare study protocol(s), CRFs, and questionnaires,
- Perform power calculations/sample size calculations,
- Prepare/validate data handling manuals and statistical analysis plans in collaboration with the statisticians (when appropriate),
- Perform data analysis (when necessary),
- Summarize results of the analysis and draw conclusions,
- Determine likely sources of bias, limitations of study, sample selection etc.,
- Prepare and review study reports,
- Actively participate in the creation of technical documents, working tools and research regarding relevant issues of interest for the company,
- Interact with the other departments of the company to provide knowledge and support in the preparation, conduct and analysis of epidemiological studies,
- Participate in client meetings and bid preparations, with exposure to the project management lifecycle,
- This position reports to the Director of Methodology & Statistics.
As an Epidemiologist and Scientific Advisor your participation in Scientific Committees may be required and you will build effective partnerships with Key Opinion Leaders and Healthcare Professionals. You will have the opportunity to develop strong oral and written communication skills through presenting at congresses and participating in the development of publications as well as other scientific communication materials.
PROFILE
- PhD, MPH-MSc Statistics or Epidemiology with a broad medical/scientific background and with a significant experience in Medical Statistics,
- Previous experience working with Public Health Insurance and/or Governmental Agencies preferred,
- Scientific accuracy,
- Strong customer focus,
- English and French bilingual.
ADVANTAGES
- Competitive Salary Package,
- Group Insurance Coverages,
- Flexible work hours with core business hours 10-16h,
- Work from home 2 days/week, rest of the week in the Malakoff office (bordering suburb of Paris on metro line),
- 5 weeks of holidays plus 10 extra days.
THE COMPANY
ClinSearch is a contract research organization providing clinical evaluation services.
Read more about our company: https://www.clinsearch.net and https://www.edclin.com
CONTACT
Bronwyn SECOURGEON bronwyn.secourgeon@clinsearch.net for additional information or to provide your CV.
Clinical Research Associate (Paris based)
ClinSearch is a European Healthcare Organization which develops innovative solutions and apps in Clinical Research, Patient-Centered Healthcare Systems, Market Access and Public Health.
We are looking for a Clinical Research Associate (CRA) to join our Clinical Research team located in the Paris Region, France. The successful candidate will preferably have good knowledge of ISO guidelines within Medical Device Sector and ICH guidelines for the development of medicines.
The CRA will be responsible for coordinating and performing clinical monitoring activities and site management. He/she will contact study sites in France, and therefore must be a French speaker (with good level of English). It is anticipated that the CRA will travel between 3 and 4 days per week within France. European travel may be required from time to time.
SKILLS, DUTIES AND RESPONSIBILITIES
- Excellent French language and grammar skills;
- Good level of English;
- Able to travel 60 to 80% of the time;
- Good oral and written communication skills;
- Good organizational and time management skills;
- Attention to detail, and able to take initiative and work with changing priorities;
- Flexibility and adaptability;
- Good computer skills: good knowledge of Microsoft Office and the ability to learn appropriate software;
- Ability to work closely with clinical personnel and the Principal Investigator to ensure that clinical documents are produced to the standards required by Good Clinical Practice (GCP);
- Ensure accurate and complete documentation of all clinical study source documents and/or forms according to company’s SOP, GCP and other applicable guidelines;
- Compile study documents;
- Perform clinical data entry and Quality Control when required;
- Carry out admin tasks including archiving; and
- Perform other work as assigned;
Qualifications
BS or Master’s degree in Life Sciences/Psychology/Sociology and, preferably, at least 6 months of experience in Pharma industry or CRO.
ADVANTAGES
- Competitive Salary Package,
- Group Insurance Coverages,
- Flexible work hours with core business hours 10-16h,
- Work from home 2 days/week, rest of the week in the Malakoff office (bordering suburb of Paris on metro line)
- 5 weeks of holidays plus 10 extra days.
THE COMPANY
ClinSearch is a contract research organization providing clinical evaluation services.
Read more about our company: https://www.clinsearch.net and https://www.edclin.com
CONTACT
Bronwyn SECOURGEON bronwyn.secourgeon@clinsearch.net for additional information or to provide your CV.
