Who Are We?
Founded in 1997 and built upon 26+ years of dermatology-specific experience, we are the only full-service dermatology CRO that takes products from concept to approval.
Voted one of San Diego’s Top Workplaces, we take pride in maintaining a company culture that values collaboration, diversity of background and thought, and dedicated talent.
When you join Therapeutics, you are not a number or a cog in the wheel, you are valued for your unique and important contributions that you bring to our team and our clients.
Who Are You?
You are a dedicated individual who is passionate about your work and you want to join a team that believes a company is only as successful as its people.
You lead with humility and know that your individual contribution is important to the team so you take pride in delivering great work.
You believe anything worth doing, is worth doing right.
You communicate clearly and have great attention to detail.
You love to collaborate with the team but are able to think on your feet to problem-solve independently.
What is the Primary Objective of the Clinical Data Associate?
Provide support to the Data Management (DM) department.
This will include administrative tasks, data entry of clinical trial data into study databases, participation in database validation, providing study status metrics and reports, and data review under the supervision of the lead Clinical Data Manager (CDM) to ensure the completeness, accuracy, and consistency of the data collected during clinical trials.
Your Main Responsibilities and Duties Include:
Supporting data management activities to meet project timelines.
Reviewing documents associated with data collection for paper CRFs: data handling conventions and data entry instructions.
Participating in study-specific database validation.
Performing pre-entry CRF reviews, data entry, and data verification, including resolution of any data clarification forms, as needed.
Performing data review under the supervision of the lead CDM.
Providing database administration support and EDC user training for clinical sites, clinical monitors, and clinical project managers.
Assisting lead CDM with ensuring all study specific documentation is filed appropriately in the study-specific Trial Master File.
Managing and prioritize data management activities to meet project schedules under supervision of lead CDM and/or Management.
Assisting with reporting on required data management metrics to ensure efficient review of data.
Providing EDC user support and training, including creating standard presentations and training documentation.
To Succeed in this Position:
You should have a scientific background (Bachelor’s degree or equivalent knowledge and experience).
Some relevant industry and/or data experience is preferred but not required.
Previous experience using electronic data capture (EDC) platforms and MS excel is desired.
Excellent written and oral communications skills, with the ability to handle multiple tasks and be detailed-oriented is essential.
The most likely starting base pay range for this position is $64,000 - $66,500 per year.
Several factors, such as experience, tenure, skills, geographic location and business needs will determine an individual’s exact level of compensation.
We at Therapeutics, Inc.
are committed to providing an environment of mutual respect where equal employment opportunities are available to all applicants and team members without regard to race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.
If you are smart and good at what you do, we welcome you to apply!
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