Clinical Trial Coordinator (m/f/d) - #10525666

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Job Description

We are a research-driven biopharmaceutical company. Our mission is built on the simple premise that if we “follow the science” that great medicines can make a significant impact to our world. We believe that a research-driven enterprise dedicated to world-class science can succeed by inventing medicine and vaccine innovations that make a difference for patients across the globe.

Our Clinical Research and Pharmacovigilance team push the boundaries of global healthcare through research and innovation. Through clinical trials and surveillance, we ensure the safety and efficacy of our existing and pipeline products to produce safe, effective, innovative medicine.

We are continually striving to improve the understanding of health care within the local community. Our site in 1100 Vienna (ICON Tower) is a strategic location for the distribution of our high quality and innovative health care products, as well as digitally integrated solutions for our patients and clients. To ensure sustainable company growth, we continually aim to offer attractive career opportunities for more than 170 employees at our Vienna site.

Clinical Trial Coordinator (m/f/d)

As a Clinical Trial Coordinator you are responsible for comprehensive trial and site administration in Austria. The person prepares, collates, distributes and archives clinical documents and ensures timely maintenance of tracking and reporting tools. The role is critical to meet planned Site Ready dates. The CTC is collaborating at local level closely with the country operations manager (COM), the project manager (CRM) and the clinical research associate (CRA). Furthermore, the CTC is managing payments according to contracts with clinical trial sites.

Our Clinical Research and Pharmacovigilance team push the boundaries of global healthcare through research and innovation. Through clinical trials and surveillance, we ensure the safety and efficacy of our existing and pipeline products to produce safe, effective, innovative medicine.

Responsibilities

Trial and site administration:

• Tracking (e.g. essential documents) and reporting (e.g. Safety Reports)
• Ensuring collation and distribution of study documents
• Updating databases and trackers
  
  

Document Management

• Preparing documents and correspondence
• Collating, distributing and archiving clinical documents
• Preparing Investigator trial file binders
  
  

Regulatory & Site Start-Up Responsibilities, In Collaboration With Country

• Providing to and collecting from investigators documents for site start-up and submissions
• Obtaining, tracking and updating study insurance certificates
• Supporting preparation documents for EU CTR submission
  
  

Budgeting, Agreement And Payments, In Collaboration With Finance/budgeting Representatives

• Calculating and executing payments to investigators
• Controlling trial site payments against budget, tracking payments from site set-up until close-out
• Maintaining tracking tools
  
  

Qualifications

• Completed job training (office management, administration, finance, health care preferred) or Bachelor’s Degree
• Good understanding of Global, Country/Regional Clinical Research Guidelines and ability to work within these guidelines
• Hands on knowledge of Good Documentation Practices
• Good IT skills (use of MS office, use of some clinical IT applications on computer) - strong MS Excel skills required
• ICH-GCP Knowledge appropriate to role
• Effective time management, organizational and interpersonal skills, conflict management
• Ability to set priorities and handle multiple tasks simultaneously in a changing environment
• Works effectively in a matrix multicultural environment
• Able to work independently
• Excellent communication skills
• Proactive attitude to solving problems / proposing solutions
• Excellent verbal and written communication skills in German and English
  
  

We offer an attractive salary, outstanding social benefits and an exciting work environment with varied tasks in an international environment. The minimum annual salary for this position is EUR 39.900,- and varies according to the qualifications and experience of the successful candidate. We are looking forward to receiving your application.

We are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. The fastest way to breakthrough innovation is when diverse ideas come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively. We are an equal opportunity employer, committed to fostering an inclusive and diverse workplace.

Current Employees apply HERE

Current Contingent Workers apply HERE

Secondary Language(s) Job Description

NA

Search Firm Representatives Please Read Carefully

Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.

Employee Status

Regular

Relocation:

VISA Sponsorship

Travel Requirements:

Flexible Work Arrangements

Not Applicable

Shift

Valid Driving License:

Hazardous Material(s)

Job Posting End Date:

07/2/2024

• A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.
  
  

Job Posting End Date:07/02/2024

A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.

Requisition ID:R292370