Sr Clin Res Assoc Ii

1) The below statements are intended to describe the general nature of the job and are not intended to be an exhaustive list of all responsibilities, skills and duties.

2) 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; liaise with vendors; and other duties, as assigned

3) Responsible for all aspects of site management as prescribed in the project plans

4) General On-Site Monitoring Responsibilities:
5) Ensure the study staff who will conduct the protocol have received the proper materials and instructions to safely enter patients into the study

6) Ensure the protection of study patients by verifying that informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements

7) Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document review

8) Monitor data for missing or implausible data

9) Ensure the resources of the Sponsor and Covance are spent wisely by performing the required monitoring tasks in an efficient manner, according to SOPs and established guidelines, including managing travel expenses in an economical fashion according to Covance travel policy

10) Ensure audit readiness at the site level

11) Travel, including air travel, may be required and is an essential function of the job.

12) Prepare accurate and timely trip reports

13) Manage small projects under direction of a Project Manager/Director as assigned

14) Serve as lead monitor for a protocol or project, and may assist in establishing monitoring plans and trip report review as assigned

15) Review progress of projects and initiate appropriate actions to achieve target objectives

16) Organize and make presentations at Investigator Meetings

17) Participate in the development of protocols and Case Report Forms as assigned

18) Participate in writing clinical trial reports as assigned

19) Interact with internal work groups to evaluate needs, resources and timelines

20) Act as contact for clinical trial supplies and other suppliers (vendors) as assigned

21) Responsible for all aspects of registry management as prescribed in the project plans

22) Undertake feasibility work when requested

23) Conduct, report and follow-up on Quality Control (QC) visits when requested

24) Recruitment of potential investigators, preparation of EC submissions, notifications to regulatory authorities, translation of study-related documentation, organization of meetings and other tasks as instructed by supervisor as assigned

25) Negotiate study budgets with potential investigators and assist the Covance legal department with statements of agreements as assigned

26) Track and follow-up on Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs

27) Independently perform CRF review; query generation and resolution against established data review guidelines on Covance or client data management systems as assigned by management

28) Assist with training, mentoring and development of new employees, e.g. co-monitoring

29) Coordinate designated clinical projects as a Local Project Coordinator (with supervision, if applicable), and may act as a local client contact as assigned

30) Perform other duties as assigned by management

Fortrea is proud to be an Equal Opportunity Employer:
As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.

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