Sr Associate, Clinical Research

Let's talk about some of the key responsibilities of the role :

• As an investigator site facing role, the Sr. CRA will act as a customer advocate through a study life cycle.
• Understand and support study goals in alignment with corporate goals.
• Organize and maintain clinical study documentation (e.g., Trial Master Study Files) including preparation for internal / external audits, final reconciliation and archival.
• Where appropriate, responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits and appropriate documentation (confirmation, follow-up letters, communication logs, as required).
• When monitoring has been delegated to a CRO, provides Sponsor oversight of monitoring activities.
• Assists in the development of study specific monitoring procedures and guidelines.
• Involved in the development or review of protocols, Case Report Forms (CRFs), informed consent forms and any other study-related documents as assigned.
• Assists in managing the identification, selection and feasibility processes of study sites.
• Ensures the study sites have received the proper materials and instructions to safely enter patients into the study; helps to train the study staff in conducting the study per GCP and in performing procedures per protocol.
• Ensures the protection of study patients by verifying that informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements.
• Where appropriate, ensures the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document review and monitors for missing or implausible data.
• Prepares accurate and timely trip reports or site audit reports in accordance with Good Clinical Practice Guidance E6 R2 and internal SOPs.
• Interacts with internal groups to evaluate needs, resources and timelines.
• Acts as a contact for clinical trial supplies and other suppliers (vendors) as assigned.
• Supports the revision and implementation of Clinical Affairs SOPs / procedures.
• Supports inspection readiness for the company, to ensure its contractors and vendors are prepared for FDA and other Health Authority GCP inspections.
• Supports oversight of Trial Master Files.
• Provides support to Clinical Development and Operations for clinical planning, start-up, execution and close-out.

Factors for Success :

A Few Other Details Worth Mentioning :

At Tarsus, we understand the importance of attracting and retaining top talent. The expected base pay range for this position is $105,000 - $147,000 plus bonus, stock equity, and comprehensive benefits. The base pay range reflects the target range for this position, but individual pay will be determined by additional factors such as job-related skills, experience and relevant education or training. Our benefits include health, dental and vision insurance benefits to ensure your well-being. We believe in work-life balance and offer generous paid time off, including vacation, holidays, and personal days. For more details regarding Tarsus benefits, please visit : https : / / alliantbenefits.cld.bz / 25tarsusbenesnap.

LI-Hybrid

LI-Remote

Tarsus Pharmaceuticals, Inc. is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex including sexual orientation and gender identity, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law.

Salary : $105,000 - $147,000