Clinical Research Associate

Job Title: Clinical Research Associate

Job Summary:

We are seeking a highly motivated Clinical Research Associate to join our Clinical Operations team in Zurich. As a Clinical Research Associate, you will play a critical role in supporting the timely delivery of clinical investigations in collaboration with our Clinical Research Managers.

Main Responsibilities:

• Support the delivery of clinical investigations in accordance with regulatory requirements and quality standards.
• Perform monitoring visits, including site qualification, study site initiation, routine monitoring, and study site closure visits.
• Ensure source data verification and timely query resolution.
• Assist in investigation start-up activities, including site selection visits and review of regulatory documents.
• Establish and maintain regular contact with investigators and ethics committees as needed.
• Prepare and maintain investigator files, center files, and study master files.
• Communicate project-specific information to/from trial sites and document communication with investigators and teams.
• Present at and participate in investigator meetings, study trainings, and meetings as assigned.
• Support statistical evaluation of study results within clinical operations.
• Support the delivery of clinical documentation needed in product development projects.
• Screen and identify business and product-relevant scientific literature as assigned.

Requirements:

• A medical-related scientific degree (e.g. Bachelor, Master, Nursing qualifications).
• Strong knowledge of ISO GCP and ICH-GCP Guidelines.
• Minimum 1-2 years of experience in various clinical trial activities within a medical device industry, preferably dentistry.
• Knowledge of the dentistry sector and a strong scientific understanding are preferred.
• Good interpersonal skills.
• Ability to work both independently and collaboratively within a team.
• Fluency in English (reading and writing), any additional language is an advantage.
• Strong interest in data analyses, graphing, and plotting results, and report writing.
• Willingness and ability to travel, as required (25%).

Operating Company: Nobel Biocare

Envista and its family of companies will not accept unsolicited resumes from any source other than directly from a candidate. Envista will consider unsolicited referrals and/or resumes submitted by vendors such as search firms, staffing agencies, professional recruiters, fee-based referral services, and recruiting agencies (Agency) to have been referred by the Agency free of charge and Envista will not pay a fee for any placement resulting from the receipt of such unsolicited resumes. An Agency must obtain advance written approval from Envista's internal Talent Acquisition or Human Resources team to submit resumes, and then only in conjunction with a valid fully-executed contract approved by the Global Talent Acquisition leader and in response to a specific job opening. Envista will not pay a fee to any Agency that does not have such agreement and written approval in place.