*Hi,*


Hope you are doing well !

My name is *Steven* and I am a Recruiter with *Infotree Services*. With
reference to your resume registered at *Monster.com*.

I have an urgent opening with me, which appears to be a potential match for
the client's requirement. I have listed the job description for your
reference.

Please let me know if you would be interested in this position.

If so, please send me a copy of your updated resume with contact details
and the best time to reach you.

I will appreciate your response at the earliest, as the manager tends to
move fast !



*Job Details** :*



*Job Title*

*Senior Medical Data Specialist *CODING *(Pharmaceutical Industry)* *2306*

*Project Location*

*Woodcliff Lake, NJ 07677*

*Duration*

*12+ months/Contract*



*Job Description** :*


Senior Medical Data Specialist CODING

Responsible for the selection codes using MedDRA and WHODD terminologies,
which most accurately describe each panel according to established coding
guidelines and conventions
Responsible for review of appropriate codes of reported terms in clinical
trials not limited to adverse events, medical history and medications.
Ensures that the term is clear, appropriate and complete as per
investigator’s entry on the CRF otherwise, he/she is responsible for the
coding query.
Familiar with grouping of terms for Adverse events of special interest or
prohibited medications in a clinical trial setting.

Quantitative analysis – Performs a comprehensive review for the all the
reported terms and coding assignments To assure the presence of all coding
hierarchy in the CRFs not limited to LLT, PT and SOC and Trade name,
Preferred Name ATC 2 and ATC 4 and their respective dictionary versions.

Qualitative analysis – Evaluates the record for coding consistency and
adequacy. Ensures that the selected codes accurately reflect the term as
provided by the investigator. Reviews the codes for ICH compliance and
adherence to coding guidelines and conventions. Adequate Clinical Data
review.

Performs all duties according to company policy and regulations and
guidance. Performs other duties assigned by the Director/Sr Manager or
designee. No travel required.

QUALIFICATIONS:
- A graduate of allied health care related course with commensurate
experience in data management
- Minimum of 5 years coding experience required
- At least 2 years of Coding in Clinical Research/Data Management.
- Strong knowledge of ICH guideline, or adequate background and have
attended seminars for MedDRA and WHODD use
- Knowledge of coding tool Central coding, INFORM a plus
- Proficiency on all related regulations, GCP, and Good Clinical DM
Practice
- Computer proficiency and knowledge of medical terminology
- Expertise on use of Excel
- Strong oral and written communication skills

We are looking for someone who is enthusiastic and willing to take a
challenge in a fast growing company. Willing to explore further
understanding of Clinical development from Data base design to Day to Day
data Cleaning until Regulatory Submission.






*Thanks & Regards,*

Steven - Associate Technical Recruiter

Phone (Direct): 734-888-8174

Email: ste...@infotreeservice.com <st...@infotreeservice.com> | Website:
www.infotreeservice.com

LinkedIn:  https://www.linkedin.com/pub/steven-fernandez/104/956/240

Hangout: steven.usrecruiter | Yahoo: steven.usrecruiter

Mailing Address: 215 Ann Arbor Rd. Suite 304 Plymouth, MI 48170

-- 
You received this message because you are subscribed to the Google Groups 
"US_IT.Groups" group.
To unsubscribe from this group and stop receiving emails from it, send an email 
to us_itgroups+unsubscr...@googlegroups.com.
To post to this group, send email to us_itgroups@googlegroups.com.
Visit this group at https://groups.google.com/group/us_itgroups.
For more options, visit https://groups.google.com/d/optout.

Reply via email to