COVINGTON, LAPosted 30+ days ago

Job summary

• Job post source

  This job is directly from Tandem Clinical Research

• Job overview

  The Clinical Site Manager at Tandem Clinical Research oversees clinic operations and staff to ensure clinical trials are conducted efficiently and according to protocols.

• Responsibilities and impact

  The role involves managing daily clinic operations, supervising and training staff, organizing clinical trial activities, ensuring compliance with protocols and regulations, handling specimens and data, and supporting quality assurance and outreach efforts.

• Experience and skills

  Candidates must have strong leadership, organizational, communication, multi-tasking skills, ability to handle confidential information, technical proficiency with office and study equipment, and effective time management.

Company overview

Tandem Clinical Research is a company that specializes in conducting clinical trials and research studies, primarily focusing on advancing medical science and improving patient care. They generate revenue by partnering with pharmaceutical companies, biotechnology firms, and medical device manufacturers to conduct trials that test the safety and efficacy of new treatments and therapies. Founded with a commitment to innovation and quality, Tandem Clinical Research has built a reputation for its rigorous approach to clinical trial management and its ability to deliver reliable and timely results. The company is known for its collaborative work environment and dedication to ethical research practices, making it an attractive employer for those passionate about contributing to medical advancements.

How to land this job

• Tailor your resume to highlight leadership and clinic operations management experience, emphasizing your ability to oversee clinical trial activities and staff supervision as outlined in the Clinical Site Manager role at Tandem Clinical Research.

• Focus on showcasing your knowledge of regulatory compliance, protocol adherence, and quality control measures, as these are critical components of the job description.

• Apply through multiple platforms such as Tandem Clinical Research’s official corporate careers page, LinkedIn job postings, and other reputable clinical research job boards to maximize your application visibility.

• Connect with current employees or managers in the clinical operations or site management division at Tandem Clinical Research on LinkedIn; start conversations with ice breakers like commenting on recent clinical trial advancements or expressing interest in their approach to trial compliance and staff training.

• Optimize your resume for ATS by incorporating keywords from the job description such as 'clinical trial management,' 'protocol compliance,' 'staff supervision,' 'regulatory standards,' and 'data management' to ensure your resume passes automated screenings.

• Utilize Jennie Johnson's Power Apply feature to automate tailored applications, identify multiple application channels, and discover LinkedIn connections for networking, allowing you to focus more on preparing for interviews and advancing your clinical research career.