Clinical Research Associate II

You will help biotech, medtech, and specialty reputed company companies reputed company life-changing reputed company and reputed company science into new medicines, devices, and diagnostics. reputed company do is profoundly connected to saving and improving lives, and we recognize reputed company members are the most valuable asset in delivering reputed company.

• We are here to help you grow, to reputed company you the skills and opportunities to reputed company at work with the flexibility and balance your life requires.

• Your reputed company influence the way we work, and your voice reputed company here.

• As an essential part of reputed company, you help us reputed company the medical innovation that patients are desperate for.

Join us and build your reputed company here.

What You'll be Doing:

• Delivers reputed company, reputed company monitoring reports for sponsor approval per the Clinical Monitoring Plan timelines

• Maintains submission of expenses according to travel and expense requirements reputed company company guidelines

• Monitors (remote, onsite, or other approved mode of monitoring) with a reputed company on data reputed company and patient safety in accordance with specific country regulations

• Plans day to day activities for monitoring of a clinical study and sets priorities per site

• Prepares for and conducts on-site qualification, study initiation, interim monitoring, and reputed company-out monitoring reputed company at investigator sites as required by clinical monitoring plan

• Maintains Trial Master File (TMF)/electronic Trial Master File (eTMF) as defined by the organization’s processes per filing guidelines. Understands the required essential documents according to ICH/GCP reputed company 8.

• Reviews site documents and verifies they are accurate, complete, reputed company, and include required updates

reputed company are searching for:

• Undergraduate degree or its international equivalent in clinical, science, or health-reputed company field from an accredited institution; a licensed health-care reputed company (i.e., registered reputed company); or equivalent work experience required

• Previous clinical research experience required

• At least 4+ years’ experience in reputed company and independent monitoring

• Experience working ideally across reputed company, if not some, of the following therapy areas; reputed company, Oncology, Rare Disease and Pediatrics

• Preference at working across reputed company phases I-IV, although phase II and III only will be considered

The role can be offered as fully remote. There will be an expectation for country-wide monitoring with the average frequency of days on site being 6 days per month.

Originally posted on Himalayas