Research Data Associate

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Fahrenheit IT
Project, Management, Biology, Protocol, Research, Project Manager, Medical Device, IT
Contract W2
Work from home not available Travel not required

Job Description

Id: 177757 Location: Boston, MA Job Type: Contract to Hire One of our client, a multidisciplinary and leading scientific organization , focusing on achieving research advances in all aspects of cancer care is seeking for multiple (3-5 openings) Clinical Data Associate reporting to Project Coordinator, Data Management located in Boston, MA . ***We are looking for recent graduate with exposure to clinical research/biology during internships or volunteer work*** Please apply if you are a recent grad in Biology/Science/Pharmaceutical Science, looking to start your pharmaceutical career!!!

We also have multiple opportunities with highly motivated Protocol Associate, Pharmaceutical Liaison, Clinical Research Associate, Clinical Project Manager and more.

These opportunities are Contract-to-hire (W2/1099/C2C) roles. If you are interested in aligning with a highly regarded organization that values quality and integrity and fosters an environment where teamwork and professionalism thrive, then don't hesitate to contact Rose Chu, VP in Pharmaceutical & Biotech Services Group at #610-822-1256 for questions.

Company offer abundant opportunities for motivated pharmaceutical professionals to pursue their scientific/clinical interests, make an impact and maximize their growth potential. Please find the qualifications and requirements below. If you feel that this position is one that you are excited about and qualified for, please send over your most recent CV. We are always interested in talking to candidates for current AND future opportunities! ***Please respond directly at rchu@gesnetwork.com with your resume attached -WORD document***

Education & Experience

A Bachelor's degree or equivalent work and/or relevant professional experience is required
Backgrounds in Medical, Biological sciences, Oncology, or Clinical Trials are strongly preferred
Recent graduate with exposure to clinical research/biology during internships or volunteer work
Proficiency in database and word processing skills, and MS Office
Knowledge/experience with electronic data submission is a plus

Responsibilities:

Responsible for the quality control of patient data on one or more studies, working with Clinical Research Associates at member institutions, physicians and statisticians throughout this process.
Review and evaluation of clinical patient data utilizing the electronic data capture system Medidata Rave®.
Assist with the creation and validation of electronic case report forms and edit checks for their assigned studies.
Using a study specific Data Management Plan, review site reported data elements, generate manual queries, resolve answered queries.
Perform serious adverse event reconciliation between Rave® and the National Cancer Institute's safety database.
Review treatment information, evaluate response to treatment, and ensure follow-up and survival data are accurately coded and updated in the database in a timely way.
Work with the Study Chair to perform final case review. Review and provide input for protocols in development.
Assist the study chair and statistician with the preparation of the database for analysis

Qualifications:

Bachelor's degree or equivalent work and/or life experience; Backgrounds in Medical, Biological sciences, Oncology, or Clinical Trials are strongly preferred
Knowledge/experience with electronic data submission a plus,
Proficiency in database and word processing skills, and MS Office
Excellent written and verbal communication skills; Strong customer service skills
Attention to detail; Reliability

As a country leading clinical company, company offers comprehensive benefits package. Interested individuals are encouraged to contact or submit their CV to the following email address: rchu@gesnetwork.com

Keywords: recent graduate with exposure to clinical research/biology during internships or volunteer work; Science, Research Data Assistant, Clinical Data Associate, CDA, Clinical Data Management, CDC, EDC, electronic data submission, clinical patient data, Medidata Rave, creation and validation of electronic case report forms and edit checks for assigned studies, study specific Data Management Plan to review site reported data elements, generate manual queries, resolve answered queries, serious adverse event reconciliation between Rave, safety database, survival data are accurately coded, final case review, Assists the Study Chair, Clinical Data Assistant, CDA, CDM, database for analysis

We appreciate your understanding, in that; we will only be able to respond to those inquiries who meet the stated requirements. To protect our client's interests, we will not be responding to inquiries that do not contain a CV/Resume. Finally, please include the position ID (rc- Clinical Data Associate) in the subject line of your correspondence to ensure review.

Please forward your credentials in Word format through Indeed or call Rose Chu at 610-822-1256 for questions. Our clinical recruiter/manager will contact the qualified candidates IMMEDIATELY to set up interviews.

Rose Chu

Vice President - Pharmaceutical, CRO, Biotech, Medical Device

Global Employment Solutions/Fahrenheit IT

P (610)822-1256 | C (215)-317-2999 | F (610-668-5000) | rchu@gesnetwork.com

One Presidential Blvd. North, Suite 310, Bala Cynwyd, PA 19004

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Company Information

Founded in 1998, Fahrenheit IT specializes in IT consulting and direct hire staffing solutions. The company delivers the highest quality technology professionals and an array of customized IT talent solutions designed to improve productivity and drive results. The Company is deeply integrated in the communities it serves and combines significant local market intelligence with the support and resources of a nationwide company.
Dice Id : 10111360
Position Id : 177757
Originally Posted : 3 months ago

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